Shandong Xinhua Pharmaceutical Co.,Ltd
Shandong Xinhua Pharmaceutical Company Limited ("Shandong Xinhua") is in an leading position in the manufacturing technology and capacity for antipyretics and analgesics in China and is an important manufacturer in China for the drugs
Cas:98-00-0
Min.Order:1000 Kilogram
Negotiable
Type:Manufacturers
inquiryAlity Chemical Corporation
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
Aecochem Corp.
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Simagchem Corporation
Welcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
Hefei TNJ chemical industry co.,ltd
1. Quality Our products meet MSDS safe standard and we have ISO and other certificate so yan can get high quality products from our company. 2. Price We are the company which is the joint of trade and industry so we cao provide the competiti
Cas:98-00-0
Min.Order:1 Metric Ton
Negotiable
Type:Trading Company
inquiryDayang Chem (Hangzhou) Co.,Ltd.
DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:98-00-0
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryChemwill Asia Co., Ltd.
Our main production base is located in Xuzhou industry park. We are certified both to the ISO 9001 and ISO 14001 Standards, have a safety management system in place.Our R&D team masters core technology for process-design of target building block
Hebei yanxi chemical co.,LTD.
D - glucuronic acid and N - acetyl glucosamine disaccharides unit composed of hyaluronic acid (Hyaluronan), also called uronic acid, hyaluronic acid, basic structure is made up of two disaccharides unit D - glucuronic acid and N - acetyl glucosamin
Henan Tianfu Chemical Co., Ltd.
Product Name: Furfuryl alcohol Synonyms: (2-furyl)-methano;2-furanemethanol;2-Furanmethanol (furfuryl alcohol);2-Furanylmethanol;2-Furfurylalkohol;2-furfurylalkohol(czech);2-Hydroxymethyklfuran;2-hydroxymethylfurane CAS: 98-00-0
Cas:98-00-0
Min.Order:1 Gram
FOB Price: $8900.0
Type:Lab/Research institutions
inquiryHenan Sinotech Import&Export Corporation
Chemical Name: Furfuryl alcohol Synonyms: 2-Furan methanol; CAS No.: 98-00-0 Molecular Formula: C5H6O2 Furfuryl Alcohol Furfuryl alcohol is a furan derivative, also named furan methanol. It is clean to light yellow transparent liq
Cas:98-00-0
Min.Order:5 Metric Ton
FOB Price: $1.0 / 2.0
Type:Other
inquiryBaoji Guokang Healthchem co.,ltd
Our company has been in existence for 10 years since its establishment. We have our own unique team. The company integrates independent research and development, production and sales. We have established famous brands at home and abroad. At prese
Cas:98-00-0
Min.Order:1 Kilogram
FOB Price: $98.0 / 100.0
Type:Trading Company
inquiryHenan Wentao Chemical Product Co., Ltd.
Henan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Changchun Artel lmport and Export trade company
Product Detail Minimum Order Qty. 10 Gram
Cas:98-00-0
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiryHangzhou Keyingchem Co.,Ltd
Hangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
Cas:98-00-0
Min.Order:0 Metric Ton
Negotiable
Type:Lab/Research institutions
inquiryHangzhou J&H Chemical Co., Ltd.
J&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Zibo Hangyu Biotechnology Development Co., Ltd
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:98-00-0
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquiryHangzhou Lingrui Chemical Co.,Ltd.
Furfuryl alcoholAppearance:clear yellow liquid Storage:KEEP COLD Package:according to customers' requirements Application:Pharmaceuticals Transportation:By air(EMS or EUB or FedEx or TNT ect...) or by sea(FOB or CIF or CNF ect...)or according to your
HANGZHOU YUNUO CHEMICAL CO.,LTD
Superior quality, moderate price & quick delivery. Appearance:colourless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:200kg/drum, or as per your request. Application:Used as Pharmaceutical Intermedia
Siwei Development Group Ltd.
Product name: Furfuryl Alcohol CAS No.：98-00-0 Molecule Formula：C5H6O2 Molecule Weight：98.10 Purity: 99.0% Package: 200kg/drum Description：Colorless to light yellow transparent liquid Manufacture Standards：Enterprise Standard
Cas:98-00-0
Min.Order:1 Kilogram
Negotiable
Type:Trading Company
inquiryZibo Dorne chemical technology co. LTD
Product Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
Cas:98-00-0
Min.Order:1 Metric Ton
Negotiable
Type:Lab/Research institutions
inquiryHunan chemfish Pharmaceutical co.,Ltd
Appearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
Xi'an yuanfar international trade company
Best quality, best price and best service. We have a professional factory ，and production capacity isveryhigh, welcome to purchase Appearance:Colorless to light yellow color,transparent liquid Application:Furfuryl alcohol is an important organic
Cas:98-00-0
Min.Order:0 Metric Ton
Negotiable
Type:Trading Company
inquiryKono Chem Co.,Ltd
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
JINHUA HUAYI CHEMICAL CO., LTD.
Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
Hangzhou Dingyan Chem Co., Ltd
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
Wuhan Fortuna Chemical Co.,Ltd
good quality and cheap price Package:25kg/200kg Application:as intermediates Transportation:by courier/sea/air
Henan Allgreen Chemical Co.,Ltd
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Enke Pharma-tech Co.,Ltd. （Cangzhou, China ）
Cangzhou Enke Pharma Tech Co.,ltd. is located in Cangzhou City, Hebei province ,where is a famous petroleum chemical industry city?in China. Enke Pharma a high-tech enterprise ,and we are dedicated to developing and manufacturing new api,?intermediat
Zhuozhou Wenxi import and Export Co., Ltd
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:98-00-0
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAntimex Chemical Limied
Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
Synthetic route
| Conditions | Yield |
|---|---|
| With Pt(3)Co(3)/C; hydrogen In water at 35℃; under 750.075 Torr; for 10h; Reagent/catalyst; Pressure; Temperature; Solvent; Concentration; | 100% |
| With HRO/TiO2; hydrogen In water at 150℃; under 15001.5 Torr; for 3h; | 100% |
| With hydrogen In isopropyl alcohol at 179.84℃; under 22502.3 Torr; for 1.25h; Reagent/catalyst; | 100% |
-
-
98-00-0
(2-furyl)methyl alcohol
| Conditions | Yield |
|---|---|
| With water | 100% |
| Conditions | Yield |
|---|---|
| Stage #1: furfural With potassium hydroxide for 0.0833333h; Cannizzaro Reaction; Milling; Inert atmosphere; Sealed tube; Green chemistry; Stage #2: With hydrogenchloride In water for 0.0833333h; Green chemistry; | A 99% B 99% |
| With TEA; magnesium bromide In dichloromethane at 20℃; for 48h; Cannizzaro reaction; | A 90% B n/a |
| With sodium hydroxide In water at 0 - 20℃; for 12h; Reagent/catalyst; Cannizzaro Reaction; | A 88% B 83% |
| Conditions | Yield |
|---|---|
| With ethanol; [bis({2‐[bis(propan‐2‐yl)phosphanyl]ethyl})amine](borohydride)(carbonyl)(hydride)iron(II) at 100℃; for 24h; Inert atmosphere; Sealed tube; Darkness; | 99% |
| With C13H34BFeNOP2; hydrogen In tetrahydrofuran at 100℃; under 22502.3 Torr; for 18h; Autoclave; Inert atmosphere; | 95% |
| With [Ru(2-(methylthio)-N-[(pyridin-2-yl)methyl]ethan-1-amine)(triphenylphosphine)Cl2]; potassium tert-butylate; hydrogen In toluene at 80℃; under 37503.8 Torr; for 10h; | 80% |
-
-
67-47-0
5-hydroxymethyl-2-furfuraldehyde
-
-
14694-95-2
Wilkinson's catalyst
-
A
-
98-00-0
(2-furyl)methyl alcohol
-
B
-
15318-33-9, 16353-77-8, 13938-94-8
chlorocarbonylbis(triphenylphosphine)rhodium(I)
| Conditions | Yield |
|---|---|
| In further solvent(s) argon-filled glovebox, durene, bibenzyl, heating 24h at 70°C; detn. of products by GC; | A 99% B n/a |
| In further solvent(s) argon-filled glovebox, durene, bibenzyl, heating 2h at 70°C; detn. of products by GC; | A 48% B n/a |
-
-
65148-89-2
2-(furan-2-ylmethoxy)tetrahydro-2H-pyran
-
-
98-00-0
(2-furyl)methyl alcohol
| Conditions | Yield |
|---|---|
| With chloral hydrate In hexane at 0 - 5℃; for 0.5h; Inert atmosphere; | 98% |
| With methanol; Montmorillonite K-10 clay at 20℃; Methanolytic deprotection; | 95% |
| With zinc tetrafluoroborate In methanol; dichloromethane; water at 20℃; for 0.75h; | 92% |
| Conditions | Yield |
|---|---|
| With C30H34Cl2N2P2Ru; potassium methanolate; hydrogen In tetrahydrofuran at 100℃; under 38002.6 - 76005.1 Torr; for 5h; Glovebox; Autoclave; | 97% |
| With ethanol; ruthenium(bis[2‐(ethylsulfanyl)ethyl]amine)(dichloro)(triphenylphosphine); potassium tert-butylate In toluene at 80℃; for 16h; | 95% |
| With ethylmagnesium bromide; poly(methylhydrosiloxane); bis(cyclopentadienyl)titanium dichloride In tetrahydrofuran; diethyl ether for 17.5h; Ambient temperature; | 89% |
-
-
98-01-1
furfural
-
-
62-53-3
aniline
-
A
-
98-00-0
(2-furyl)methyl alcohol
-
B
-
4439-56-9
N-(furan-2-ylmethyl)aniline
| Conditions | Yield |
|---|---|
| Stage #1: furfural; aniline at 25℃; for 0.166667h; Stage #2: With sodium tetrahydroborate; toluene-4-sulfonic acid at 25℃; for 0.166667h; | A n/a B 97% |
| With hydrogen; edetate disodium; iron(II) sulfate In water at 150℃; under 20686.5 Torr; for 12h; Title compound not separated from byproducts.; | A 7 % Chromat. B 72 % Chromat. |
| Stage #1: furfural at 40℃; for 0.166667h; Stage #2: aniline With sodium tetrahydroborate at 40℃; for 3h; Stage #3: With methanol at 0℃; for 0.5h; chemoselective reaction; |
-
-
121389-55-7
tert-butyl(furan-2-ylmethoxy)dimethylsilane
-
-
98-00-0
(2-furyl)methyl alcohol
| Conditions | Yield |
|---|---|
| With Decaborane In methanol at 20℃; for 0.5h; | 96% |
| With sodium hydride In N,N,N,N,N,N-hexamethylphosphoric triamide at 25℃; for 8h; | 93% |
| With acetyl chloride In methanol at 20℃; for 0.583333h; | 85% |
| With tin(ll) chloride In water for 5h; Heating; | 85% |
| With acetonyltriphenylphosphonium bromide In methanol; dichloromethane at 20℃; for 0.166667h; | 83% |
| Conditions | Yield |
|---|---|
| With palladium nanoparticles deposited on porous SBA-15 In cyclohexane at 130℃; for 12h; Reagent/catalyst; Temperature; Solvent; Time; Molecular sieve; | 96% |
| With palladium/alumina In hexane at 145℃; under 45004.5 Torr; for 4h; Catalytic behavior; Reagent/catalyst; Green chemistry; | 95.6% |
| With zirconium hydroxide; ethanol at 150℃; Flow reactor; | 84% |
-
-
98-00-0
(2-furyl)methyl alcohol
| Conditions | Yield |
|---|---|
| With sodium hydroxide In water Inert atmosphere; | 95% |
-
-
98-01-1
furfural
-
A
-
98-00-0
(2-furyl)methyl alcohol
-
B
-
4464-77-1, 69314-24-5, 69314-25-6, 116204-42-3
1,2-di-furan-2-yl-ethane-1,2-diol
| Conditions | Yield |
|---|---|
| With potassium hydroxide at 20℃; under 760.051 Torr; Reagent/catalyst; Electrochemical reaction; Green chemistry; | A n/a B 94% |
| With sodium hydroxide; aluminium In methanol; water for 0.166667h; pinacol coupling; microwave irradiation; | A 10% B 70% |
| With acetic acid; zinc In water at 20℃; for 0.333333h; Green chemistry; | A 39% B 51% |
| With naphthalene; lithium; manganese(ll) chloride In tetrahydrofuran at 50 - 54℃; for 1h; sonication; | A 12% B 37% |
| With manganese; 2,4,6-collidine hydrochloride In tetrahydrofuran; water at 27℃; for 24h; Inert atmosphere; Schlenk technique; Overall yield = 95 %; Overall yield = 92 mg; chemoselective reaction; |
-
-
14694-95-2
Wilkinson's catalyst
-
A
-
98-00-0
(2-furyl)methyl alcohol
-
B
-
15318-33-9, 16353-77-8, 13938-94-8
chlorocarbonylbis(triphenylphosphine)rhodium(I)
-
C
-
87-99-0
XYLITOL
| Conditions | Yield |
|---|---|
| In further solvent(s) argon-filled glovebox, durene, bibenzyl, heating 6h; | A 59% B 94% C 1% D 5% |
-
-
98-00-0
(2-furyl)methyl alcohol
| Conditions | Yield |
|---|---|
| With silica gel In ethyl acetate; Petroleum ether | 94% |
| With water; silica gel In methanol at 60℃; Inert atmosphere; | 88% |
| In methanol at 20℃; for 6h; Inert atmosphere; Glovebox; | 74% |
-
-
67-47-0
5-hydroxymethyl-2-furfuraldehyde
-
A
-
534-22-5
2-methylfuran
-
B
-
98-00-0
(2-furyl)methyl alcohol
-
C
-
625-86-5
2,5-dimethylfuran
| Conditions | Yield |
|---|---|
| With hydrogen In 1,4-dioxane at 180℃; under 11251.1 Torr; for 2h; Catalytic behavior; | A n/a B n/a C 93.4% |
| Conditions | Yield |
|---|---|
| With 1,4-diazabicyclo[2.2.2]octane tribromide supported on magnetic Fe3O4 nanoparticles In methanol at 20℃; for 0.0833333h; | 93% |
| With water; boric acid at 20℃; for 1h; | 87% |
| With aminosulfonic acid; water at 20℃; for 2h; | 85% |
-
-
98-01-1
furfural
-
-
108-91-8
cyclohexylamine
-
A
-
98-00-0
(2-furyl)methyl alcohol
-
B
-
4439-54-7
N-cyclohexan-1-(furan-2-yl)methanamine
-
C
-
69819-61-0
N-(furan-2-ylmethylene)cyclohexanamine
| Conditions | Yield |
|---|---|
| With hydrogen; Pd on polytris(hydroxymethyl)melamine In ethanol at 45℃; under 757.6 Torr; for 1h; Rate constant; Kinetics; activation energy, other catalysts: Pd/C, palladium on aminated and chloromethylated styrene-divinylbenzene copolymer anion exchange resin AV-17-8 matrix, other solvents: 1-propanol, 2-propanol, 1-butanol, 2-methyl-2-propanol, toluene, hexane; | A n/a B n/a C n/a D 92% |
-
-
1899-24-7
5-bromo-2-furancarboxaldehyde
-
A
-
98-00-0
(2-furyl)methyl alcohol
-
B
-
27230-58-6
(5-bromo-2-furan-2-yl)methanol
| Conditions | Yield |
|---|---|
| With lithium aluminium tetrahydride In diethyl ether at 0℃; for 2h; | A 9% B 91% |
-
-
67-47-0
5-hydroxymethyl-2-furfuraldehyde
-
A
-
98-00-0
(2-furyl)methyl alcohol
-
B
-
823-82-5
2,5-diformylfurane
| Conditions | Yield |
|---|---|
| With carbon dioxide; palladium/alumina In tetrahydrofuran at 145℃; under 45004.5 Torr; for 4h; Catalytic behavior; Reagent/catalyst; Green chemistry; | A 90.9% B 5.5% |
| With Pd/γ-Al2O3 In 1,4-dioxane at 160℃; for 16h; Inert atmosphere; Autoclave; |
| Conditions | Yield |
|---|---|
| With hydrogen at 90℃; under 15001.5 Torr; Reagent/catalyst; | A 90.5% B 8.4% |
| With hydrogen In butan-1-ol at 40℃; under 30003 Torr; for 7h; Catalytic behavior; Reagent/catalyst; | A 12% B 85% |
| With hydrogen In tetrahydrofuran at 175℃; under 7500.75 Torr; for 8h; Catalytic behavior; Pressure; Temperature; Time; chemoselective reaction; | A 10% B 79.5% |
| Conditions | Yield |
|---|---|
| With dodecatungstosilic acid; formic acid In tert-butyl alcohol for 3h; Kinetics; Activation energy; Reagent/catalyst; chemoselective reaction; | 90.1% |
| Multi-step reaction with 2 steps 1.1: formic acid / tetrahydrofuran; dimethyl sulfoxide / 150 °C 2.1: Cp*Ir(TsDPEN); triethylamine / tetrahydrofuran; dimethyl sulfoxide / 0.08 h / 40 °C 2.2: 40 °C View Scheme | |
| Multi-step reaction with 2 steps 1: sodium chloride; aluminum (III) chloride / iso-butanol / 140 °C / Autoclave 2: isopropyl alcohol; iron oxide / 5 h / 160 °C / Autoclave View Scheme |
-
-
98-01-1
furfural
-
-
67-63-0
isopropyl alcohol
-
A
-
98-00-0
(2-furyl)methyl alcohol
-
B
-
623-15-4
4-(furan-2-yl)but-3-en-2-one
-
C
-
113984-01-3
isopropopyl (2-methylfuran) ether
| Conditions | Yield |
|---|---|
| With iron oxide at 160℃; for 5h; Reagent/catalyst; Temperature; Autoclave; | A 90.1% B n/a C n/a |
| at 219.84℃; under 760.051 Torr; Temperature; Flow reactor; Inert atmosphere; | |
| With 2 wt% MgO loaded on amorphous silica at 159.84℃; under 3750.38 Torr; for 12h; Reagent/catalyst; Inert atmosphere; | A 9.2 %Chromat. B 9.2 %Chromat. C 14.2 %Chromat. |
| Conditions | Yield |
|---|---|
| With strain of the zygomycete fungus S. racemosum MUT 770 In dimethyl sulfoxide for 72h; Enzymatic reaction; | 90% |
| Stage #1: 2-furanoic acid With trimethylphenylsilane; C69H55ClP3Ru In tetrahydrofuran at 60℃; for 16h; Glovebox; Stage #2: With hydrogenchloride In tetrahydrofuran; water at 20℃; for 1h; Glovebox; chemoselective reaction; | 65% |
| With sodium tetrahydroborate; N,N-dimethylchloromethyleniminium chloride 1.) acetonitrile, THF, 0 deg C, 1 h; 2.) acetonitrile, THF, N,N-dimethylformamide, -78 deg C to -20 deg C, 2 h; Yield given. Multistep reaction; |
| Conditions | Yield |
|---|---|
| With lipase B from Candida antarctica immobilized on Immobead 150 In aq. phosphate buffer at 40℃; for 0.333333h; pH=7.4; | 89% |
| With methanol; potassium permanganate; trimethylsulphonium iodide at 25℃; under 760.051 Torr; chemoselective reaction; | 80% |
| With methanol; potassium permanganate at 25℃; chemoselective reaction; | 78% |
| With [t-Bu2SnOH(Cl)]2 In methanol at 30℃; for 24h; Deacetylation; | 82 % Chromat. |
| [t-Bu2SnOH(Cl)]2 In methanol at 30℃; for 24h; | 82 % Chromat. |
| Conditions | Yield |
|---|---|
| With sodium tetrahydroborate; nickel(II) chloride hexahydrate In methanol at 20℃; for 4h; chemoselective reaction; | 86% |
| Conditions | Yield |
|---|---|
| With C22H21ClN3RuS2(1+)*F6P(1-); isopropyl alcohol; potassium hydroxide In acetonitrile at 80℃; for 3h; Catalytic behavior; Concentration; Reagent/catalyst; | 85% |
-
-
98-00-0
(2-furyl)methyl alcohol
| Conditions | Yield |
|---|---|
| With sodium hydroxide In water Schlenk technique; Inert atmosphere; | 85% |
| With sodium hydroxide In water |
| Conditions | Yield |
|---|---|
| With hydrogen at 160℃; under 760.051 Torr; for 24h; Reagent/catalyst; Temperature; | A n/a B 84.7% |
| With hydrogen; CuO on Al2O3 at 250℃; Product distribution; gas phase, flow reactor, oth. temperature, var. ratio of reactants; | A 69.7% B 4.2% |
| With hydrogen In isopropyl alcohol at 200℃; under 22502.3 Torr; Autoclave; | A 66% B 6% |
-
-
17357-38-9
S-phenyl furan-2-carbothioate
-
-
98-00-0
(2-furyl)methyl alcohol
| Conditions | Yield |
|---|---|
| With zinc(II) tetrahydroborate In tetrahydrofuran; diethyl ether for 96h; Ambient temperature; | 84% |
| Conditions | Yield |
|---|---|
| With 3% Pd/C; hydrogen In isopropyl alcohol at 219.84℃; under 25858.1 Torr; for 5h; Inert atmosphere; | 100% |
| With hydrogen In isopropyl alcohol at 25℃; under 7500.75 Torr; for 3h; Green chemistry; | 100% |
| With palladium on activated charcoal; ammonia; hydrogen In tetrahydrofuran at 160℃; for 4h; Reagent/catalyst; Autoclave; | 100% |
-
-
98-00-0
(2-furyl)methyl alcohol
-
-
18162-48-6
tert-butyldimethylsilyl chloride
-
-
121389-55-7
tert-butyl(furan-2-ylmethoxy)dimethylsilane
| Conditions | Yield |
|---|---|
| With dmap; triethylamine In dichloromethane at -78 - 20℃; | 100% |
| With 1H-imidazole In N,N-dimethyl-formamide | 99% |
| With 1H-imidazole In N,N-dimethyl-formamide at 23℃; for 0.5h; | 97% |
-
-
98-00-0
(2-furyl)methyl alcohol
-
-
106-96-7
propargyl bromide
-
-
32904-79-3
2-((prop-2-yn-1-yloxy)methyl)furan
| Conditions | Yield |
|---|---|
| Stage #1: (2-furyl)methyl alcohol With sodium hydride In N,N-dimethyl-formamide at 0℃; for 1.5h; Stage #2: propargyl bromide In N,N-dimethyl-formamide at 20℃; Reagent/catalyst; | 100% |
| With para-chlorotoluene; lithium In tetrahydrofuran at -35 - 20℃; for 10h; Heating / reflux; | 93% |
| Stage #1: (2-furyl)methyl alcohol With sodium hydride In N,N-dimethyl-formamide at 0℃; for 0.166667h; Stage #2: propargyl bromide In N,N-dimethyl-formamide; toluene at 23℃; for 4h; | 86% |
| Conditions | Yield |
|---|---|
| With bis(2,2'-bipyridyl) copper(II) permanganate In acetone for 0.1h; Ambient temperature; | 100% |
| With 4 A molecular sieve; tetrabutylammonium perchlorate; Ru-Cu-Al-hydrotalcite In toluene at 60℃; for 3h; | 100% |
| With potassium carbonate In toluene at 70℃; for 2.5h; Reagent/catalyst; | 100% |
-
-
98-00-0
(2-furyl)methyl alcohol
-
-
22536-63-6
2-chloro-4-methoxypyrimidine
| Conditions | Yield |
|---|---|
| With sodium alkoxide | 100% |
-
-
98-00-0
(2-furyl)methyl alcohol
| Conditions | Yield |
|---|---|
| Stage #1: potassium 4-(methoxy)phenyltrifluoroborate With dmap; copper diacetate; 4 A molecular sieve In dichloromethane at 20℃; for 0.0833333h; Stage #2: (2-furyl)methyl alcohol With oxygen In dichloromethane at 20℃; for 24h; | 100% |
-
-
98-00-0
(2-furyl)methyl alcohol
-
-
819813-95-1
2-nitro-N-[2-(tetrahydropyran-2-yloxy)ethyl]benzenesulfonamide
-
-
819813-96-2
N-furfuryl-2-nitro-N-[2-(tetrahydropyran-2-yloxy)ethyl]benzenesulfonamide
| Conditions | Yield |
|---|---|
| With triphenylphosphine; diethylazodicarboxylate In toluene at 20℃; for 1h; | 100% |
-
-
504-29-0
2-aminopyridine
-
-
98-00-0
(2-furyl)methyl alcohol
-
-
46230-01-7
furan-2-ylmethyl-pyridin-2-yl-amine
| Conditions | Yield |
|---|---|
| With dichloro-[1,3-bis(4-tert-butylbenzyl)perhydrobenzimidazol-2-ylidene](p-cymene)ruthenium(II); potassium tert-butylate at 120℃; for 24h; Reagent/catalyst; Inert atmosphere; Schlenk technique; Sealed tube; | 100% |
| With [RuCl(N,N-dimethyl-1-[6-(4'-methylphenyl)pyridin-2-yl]methaneamine(-H))(dppb)]; potassium tert-butylate In tetrahydrofuran; toluene at 110℃; for 24h; Inert atmosphere; Molecular sieve; | 81% |
| With C46H45ClN4PRu(1+)*F6P(1-); potassium 2-methylbutan-2-olate In toluene at 150℃; for 18h; | 77% |
| Conditions | Yield |
|---|---|
| With dichloro-[1,3-bis(4-methylbenzyl)perhydrobenzimidazol-2-ylidene](p-cymene)ruthenium(II); potassium tert-butylate at 120℃; for 24h; Reagent/catalyst; Inert atmosphere; Schlenk technique; Sealed tube; | 100% |
| With titanium triflimide complex; pyridine ligand In toluene at 100℃; for 2h; Microwave irradiation; | 98% |
| With C36H35IrN2P(1+)*C32H12BF24(1-); potassium tert-butylate In diethylene glycol dimethyl ether at 50℃; for 24h; Inert atmosphere; | 94% |
| Conditions | Yield |
|---|---|
| In cyclohexane Inert atmosphere; Reflux; | 100% |
| In cyclohexane for 0.5h; Schlenk technique; Inert atmosphere; Reflux; | 100% |
-
-
98-00-0
(2-furyl)methyl alcohol
-
-
79-04-9
chloroacetyl chloride
-
-
51618-39-4
(furan-2-yl)methyl 2-chloroacetate
| Conditions | Yield |
|---|---|
| With pyridine In diethyl ether at 0℃; | 100% |
| Conditions | Yield |
|---|---|
| With dichloro-[1,3-bis(4-isopropylbenzyl)perhydrobenzimidazol-2-ylidene](p-cymene)ruthenium(II); potassium tert-butylate at 120℃; for 24h; Reagent/catalyst; Inert atmosphere; Schlenk technique; Sealed tube; | 100% |
| With dichloro(1‐(2‐vinyloxyethyl)benzimidazole)‐(p‐cymene)ruthenium(II); potassium tert-butylate at 120℃; for 24h; Reagent/catalyst; Schlenk technique; Inert atmosphere; | |
| With [dichloro‑[1,3‑bis(4‑phenylbenzyl)perhydrobenzimidazol‑2‑ylidene](η6-p‑cymene)ruthenium(II)]; potassium tert-butylate In neat (no solvent) at 120℃; for 24h; Reagent/catalyst; Inert atmosphere; Schlenk technique; Sealed tube; | 100 %Chromat. |
| With potassium tert-butylate; C46H56Cl2N2Ru In neat (no solvent) at 120℃; for 24h; Reagent/catalyst; Inert atmosphere; Schlenk technique; Sealed tube; | 76 %Chromat. |
-
-
98-00-0
(2-furyl)methyl alcohol
| Conditions | Yield |
|---|---|
| With pyridine In dichloromethane at 0 - 20℃; Inert atmosphere; | 100% |
| Conditions | Yield |
|---|---|
| With dmap; dicyclohexyl-carbodiimide In tetrahydrofuran at 20℃; for 3h; | 100% |
| Conditions | Yield |
|---|---|
| at 20 - 80℃; for 6h; Temperature; Reagent/catalyst; | 99.32% |
| Conditions | Yield |
|---|---|
| With 5-sulfosalicylic Acid at 118℃; under 760.051 Torr; for 10h; Catalytic behavior; Temperature; | 99.3% |
| With toluene-4-sulfonic acid at 80℃; for 4h; Reagent/catalyst; Temperature; Inert atmosphere; | 94.2% |
| With [BmimSO3H]3PW12O40; water at 110℃; for 12h; | 93% |
-
-
98-00-0
(2-furyl)methyl alcohol
-
-
109-87-5
Dimethoxymethane
-
-
126825-52-3
2-((methoxymethoxy)methyl)furan
| Conditions | Yield |
|---|---|
| With Mo(VI)/ZrO2 at 40℃; for 0.333333h; Reagent/catalyst; Reflux; Inert atmosphere; Green chemistry; | 99.2% |
-
-
98-00-0
(2-furyl)methyl alcohol
-
-
75-15-0
carbon disulfide
-
-
89712-86-7
potassium O-furfuryl dithiocarbonate
| Conditions | Yield |
|---|---|
| With potassium hydroxide In diethyl ether at 20℃; for 12h; | 99% |
| With potassium hydroxide In acetone | 67% |
| With potassium hydroxide | |
| With potassium hydroxide In tetrahydrofuran at 20℃; under 760.051 Torr; | |
| With potassium hydroxide |
| Conditions | Yield |
|---|---|
| With tin(IV) tetraphenylporphyrin perchlorate at 20℃; for 0.0833333h; | 99% |
| tetradecafluorohexane at 20℃; for 6h; | 99% |
| With [{CpHf(OH2)3}2(μ2-OH)2][OSO2C8F17]4*4H20*2THF at 20℃; for 0.0833333h; chemoselective reaction; | 98% |
| Conditions | Yield |
|---|---|
| With manganese(IV) oxide; oxygen; sodium hydrogencarbonate In water at 100℃; under 7500.75 Torr; for 24h; | 99% |
| With oxygen; 1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazolium chloride; sodium t-butanolate In dichloromethane at 20℃; for 30h; Reagent/catalyst; Molecular sieve; | 95% |
| With sodium carbonate In water at 30℃; for 40h; Wavelength; Irradiation; | 93% |
| Conditions | Yield |
|---|---|
| With 1,4-diaza-bicyclo[2.2.2]octane In dichloromethane | 99% |
| With tributylphosphine In dichloromethane for 0.0833333h; Ambient temperature; | 98% |
-
-
98-00-0
(2-furyl)methyl alcohol
-
-
59995-47-0, 59995-49-2, 61305-27-9, 61740-29-2
4-Hydroxycyclopent-2-enone
| Conditions | Yield |
|---|---|
| With sodium hydroxide In water at 240℃; Temperature; Reagent/catalyst; Solvent; Autoclave; | 99% |
| With sodium hydroxide In water at 240℃; for 0.02h; Catalytic behavior; Reagent/catalyst; Solvent; Temperature; Autoclave; | 99% |
| With sodium hydroxide In water at 240℃; for 0.02h; Reagent/catalyst; Temperature; Solvent; Concentration; | 99% |
-
-
98-00-0
(2-furyl)methyl alcohol
-
-
999-97-3
1,1,1,3,3,3-hexamethyl-disilazane
-
-
2846-62-0
(furan-2-ylmethoxy)trimethylsilane
| Conditions | Yield |
|---|---|
| With phenyltrimethylammonium tribromide In dichloromethane at 20℃; for 0.166667h; chemoselective reaction; | 99% |
| With lithium perchlorate; silica gel In dichloromethane at 20℃; for 0.0833333h; | 96% |
| With Nafion SAC-13 at 20℃; for 0.0833333h; | 96% |
-
-
98-00-0
(2-furyl)methyl alcohol
-
-
2325-27-1
N-phenyltriphenyliminophosphorane
-
-
4439-56-9
N-(furan-2-ylmethyl)aniline
| Conditions | Yield |
|---|---|
| With cesium hydroxide; palladium diacetate In toluene at 150℃; for 48h; Aza-Wittig reaction; | 99% |
| With 1,1'-bis-(diphenylphosphino)ferrocene; potassium carbonate; bis(1,5-cyclooctadiene)diiridium(I) dichloride In toluene at 110℃; for 24h; indirect aza-Wittig reaction; | 71% |
-
-
98-00-0
(2-furyl)methyl alcohol
-
-
60750-38-1
1,2,3,4-tetrahydro-1,6-dimethyl-2-oxo-4-phenylpyrimidine-5-carboxylic acid
-
-
95928-47-5
Furfuryl Ester of 1,6-Dimethyl-4-phenyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic Acid
| Conditions | Yield |
|---|---|
| With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; for 0.00833333h; Mitsunobu esterification; | 99% |
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