Purity: 99% Excellent product quality and competitive price Faxt delivery Appearance:Colorless liquid Storage:Store in cool dry place Package:170 kg/drum Application:used in the fragrance industry due to its pleasant smell. Port:Shanghai, N
Cas:111-70-6
Min.Order:1 Metric Ton
Negotiable
Type:Manufacturers
inquiryHebei Yanxi Chemical Co., Ltd. is a professional research, development and production of lead acetate benzene acetamide enterprise backbone members by local well-known entrepreneurs and professional senior engineers in the party's "low car
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
Shanghai Seasonsgreen Chemical is a high-tech research and development, production, sale and custom synthesis set in one high-tech chemical products enterprises. Our sales and marketing division is located in Shanghai, serving international pharmaceu
Cas:111-70-6
Min.Order:1 Kilogram
FOB Price: $1.0
Type:Manufacturers
inquiryAs a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem’s R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis
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
Our company engages in Sodium Tripolyphosphate (STPP) and Sodium Hexametabphosphate (SHMP) production; development of noble metal catalysts, synthesis of electronic chemical materials and general chemicals Imp&Exp trading business. The company
Cas:111-70-6
Min.Order:1 Kilogram
FOB Price: $1000.0
Type:Lab/Research institutions
inquiryOur advantages: 1. All inquiries will be replied within 12 hours. 2. Dedication to quality, supply & service. 3. Strictly on selecting raw materials. 4. Reasonable & competitive price, fast lead time. 5. Sample is available for your eva
Cas:111-70-6
Min.Order:1 Gram
FOB Price: $1.0 / 99.0
Type:Trading Company
inquiryWITH US,YOUR MONEY IN SAFE,YOUR BUSINESS IN SAFE 1)Quick Response Within 12 hours; 2)Quality Guarantee: All products are strictly tested by our QC, confirmed by QA and approved by third party lab in China, USA, Canada, Germany, UK, Italy, France et
Cas:111-70-6
Min.Order:10 Gram
FOB Price: $146.0 / 176.0
Type:Trading Company
inquiry1. Product advantages ♦ High purity, all above 98.5%, no impurities after the dissolution ♦ We will test each batch to ensure quality ♦ OEM and private brand services designed for free ♦ Various cap colors available &diam
Cas:111-70-6
Min.Order:1 Kilogram
FOB Price: $7.0 / 9.0
Type:Trading Company
inquiry1.No Less 8 years exporting experience. Clients can 100% received goods 2.Lower Price with higher quality 3,Free sample 4,We are sincerely responsible for the "product quality" and "After Service" Upbio is Specialized
Cas:111-70-6
Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
inquiryProduct Name: 1-Heptanol CAS: 111-70-6 MF: C7H16O MW: 116.2 EINECS: 203-897-9 1-Heptanol Structure 1-Heptanol Chemical Properties Melting point -36 °C (lit.) Boiling point 176 °C (lit.) density 0.822 g/mL at 25 &d
1-Heptanol CAS:111-70-6 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic intermediates,
Cas:111-70-6
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryHello, dear friend! I'm Hansen and Allen from China. Welcome to my lookchem mall! The following is a brief introduction of our company's products and services. If you are interested in our products, please contact us by emai
Minimum Order Qty. 10 Gram Supply Ability 500 Kilograms/Month Storage store in cool, dry, ventilated place 20℃ Delivery Time 3 business days after payment Payment Term TT,western union,Paypal,MoneyGram Package 10g,20g,50g,100g,500g,1KGS,
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
Best quality & Attractive price & Professional service; Trial & Pilot & Commercial Hisunny Chemical is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality intermediates, specia
Appearance:Colorless liquid Storage:Store in a cool,dry place and keep away from direct strong light Package:As customer request Application:used in the fragrance industry due to .. Transportation:Common products:Sea/Air/Courie
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
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 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
High quality, competitive price, fast delivery and first-class service we possesses have won the trust and praise of customers. Standard: BP/USP/EP The purity is equal or greater than 99%. As a supplier, we can provide high-quality products. Cle
Cas:111-70-6
Min.Order:1 Metric Ton
Negotiable
Type:Lab/Research institutions
inquiryHangzhou Huarong Pharm Co., Ltd.established since 2006 , has been actively developing specialty products for Finished Dosages, APIs, Intermediates, and Fine chemicals markets in North America, Europe, Korea, Japan, Mid-East and all over the World. Hu
1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
Cas:111-70-6
Min.Order:1 Metric Ton
FOB Price: $7.0 / 8.0
Type:Trading Company
inquiryLower price, sample is available,SDS test documents are available,large stock in warehouseAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:Fine chemical intermediates, used as the main raw material for the synthe
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
AN ISO 9001, ISO 14001, ISO 22022 CERTIFIED FACTORY,HALAL 、KOSHER、FCC AND FDA CERTIFICATE ARE AVAILABLE. Storage:1000KG Package:25/170KG per drum Application:Daily flavor, food additives Transportation:by air /by sea or by courier like DHL or Fedex P
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
Q1: Are you a manufacturer Answer: Yes, we are factory founded on 2012.Q2: How to contact with us Click "contact supplier" And then send us message the product you interest in, you will get reply within 12 hours.Q3:Which kind of payment terms do you
Acmec is a leading manufacturer and supplier of biochemical reagents and life science products. We have over 40,000 items in stock (real-time inventory) and offer discounted prices to registered members of the online store ( www.acmec.com.cn ) Appea
Cas:111-70-6
Min.Order:1 bottle
Negotiable
Type:Lab/Research institutions
inquiryConditions | Yield |
---|---|
With Triethoxysilane; potassium fluoride at 25℃; for 20h; | 100% |
With Triethoxysilane; 1,3-Diphenylpropanone; potassium fluoride at 25℃; for 7h; | 100% |
With 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane In benzene-d6 at 25℃; for 6h; Inert atmosphere; Glovebox; Sealed tube; | 98% |
1-<(tert-butyldimethylsilyl)oxy>heptane
n-heptan1ol
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran for 21h; Ambient temperature; | 100% |
With methanol at 20℃; for 2h; | 100% |
sulfonic acid functionalized nanoporous silica In methanol at 35℃; for 1.2h; | 93% |
With water; 2,3-dicyano-5,6-dichloro-p-benzoquinone In ethyl acetate at 20 - 25℃; for 26h; | 14% |
2-(heptyloxy)tetrahydro-2H-pyran
n-heptan1ol
Conditions | Yield |
---|---|
With methanol; Montmorillonite K-10 clay at 20℃; Methanolytic deprotection; | 97% |
With bismuth(lll) trifluoromethanesulfonate In methanol for 0.0833333h; Heating; | 97% |
With Oxone In methanol for 1.25h; Heating; | 82% |
With bismuth(lll) trifluoromethanesulfonate In methanol; N,N-dimethyl-formamide at 110℃; for 24h; | 67% |
Conditions | Yield |
---|---|
With sodium tetrahydroborate; palladium diacetate In methanol at 20℃; for 1h; | 96% |
heptanol trimethylsilyl ether
n-heptan1ol
Conditions | Yield |
---|---|
With Oxone In methanol for 0.15h; Heating; | 95% |
With Nafion-H(R); silica gel In hexane at 20℃; for 0.416667h; | 95% |
With ethylenebis(N-methylimidazolium) chlorochromate In acetonitrile for 1h; Reflux; | 92% |
Conditions | Yield |
---|---|
In toluene for 24h; Alkylation; reduction; Title compound not separated from byproducts.; | A 95% B 2% |
Conditions | Yield |
---|---|
With hydrogen In ethanol; benzene | 95% |
n-heptan1ol
Conditions | Yield |
---|---|
With silica gel In methanol at 50℃; for 3h; | 95% |
With methanol; silica gel at 50℃; for 3h; | 82% |
With hydrogenchloride In water | |
With methanol; silica gel at 50℃; for 1.91667h; | 88 %Spectr. |
n-heptan1ol
Conditions | Yield |
---|---|
With whole cell cultures of dichomitus albidofuscus at 24℃; for 96h; Darkness; Microbiological reaction; | 95% |
heptyl 4-methylbenzenesulfinate
A
1-Bromoheptane
B
n-heptan1ol
C
1,2-dibromoheptane
D
toluene-p-sulfonyl bromide
Conditions | Yield |
---|---|
With bromine In chloroform for 2.5h; Ambient temperature; | A 89 % Chromat. B 3 % Chromat. C 1 % Chromat. D 94% |
Conditions | Yield |
---|---|
With potassium hydroxide; tetrafluoroboric acid; sodium hydrogencarbonate; mercury(II) oxide In tetrahydrofuran 1.) room temp., 3 h; | 93% |
With water; tetra-(n-butyl)ammonium iodide; caesium carbonate In dimethyl sulfoxide at 100℃; for 24h; Schlenk technique; | 58% |
With water; tetra-(n-butyl)ammonium iodide; caesium carbonate; dimethyl sulfoxide at 100℃; for 24h; Schlenk technique; Sealed tube; | 58% |
1-heptyl 4-methylbenzenesulfonate
n-heptan1ol
Conditions | Yield |
---|---|
With cerium(III) chloride; sodium iodide In acetonitrile for 4h; tosylate cleavage; Heating; | 90% |
Conditions | Yield |
---|---|
In toluene for 0.166667h; Alkylation; reduction; dimerization; Title compound not separated from byproducts.; | A 90% B 3% C 2% |
methoxymethyl heptyl ether
n-heptan1ol
Conditions | Yield |
---|---|
phosphotungstic acid In ethanol for 3.5h; Heating; | 90% |
Conditions | Yield |
---|---|
With N-methylpyrrolidine zinc borohydride In tetrahydrofuran at 20℃; for 1.16667h; | 89% |
Conditions | Yield |
---|---|
With tert-butyl alcohol In tetrahydrofuran electrolysis (Mg electrodes, LiClO4); | 88% |
With tert-butyl alcohol In tetrahydrofuran Product distribution; Mechanism; electrolysis (Mg electrodes, LiClO4); or Al electrodes; | 88% |
With 5 wt% Re/TiO2; hydrogen In octane at 180℃; under 37503.8 Torr; for 24h; Autoclave; chemoselective reaction; | 85% |
Conditions | Yield |
---|---|
With (CH3C6H4CH(CH3)2)RuCl((NH2)2C6H4)(1+)*Cl(1-)={(CH3C6H4CH(CH3)2)RuCl((NH2)2C6H4)}Cl; water In 1,4-dioxane at 105℃; for 20h; Schlenk technique; Inert atmosphere; | A n/a B 87% |
bei der Einw.von Schweineleber-Brei; | |
With water; NADPH at 25℃; for 18h; pH=9; aq. buffer; Enzymatic reaction; |
Conditions | Yield |
---|---|
dodecacarbonyl-triangulo-triruthenium; P(C4H9)3 In pyridine at 180℃; for 10h; | 86% |
ethoxymethyl heptyl ether
n-heptan1ol
Conditions | Yield |
---|---|
phosphotungstic acid In ethanol for 3.5h; Heating; | 86% |
Conditions | Yield |
---|---|
With bis(acetylacetonate)oxovanadium; methyl 3,5-bis((1H-1,2,4-triazol-1-yl)methyl)benzoate; oxygen; sodium acetate at 120℃; for 48h; | A 79% B 86% |
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In tetrahydrofuran; hexane at -78℃; for 0.166667h; | 85% |
Conditions | Yield |
---|---|
In toluene for 0.166667h; Alkylation; reduction; dimerization; Title compound not separated from byproducts.; | A 85% B 9% C 2% |
heptyl boronic acid
n-heptan1ol
Conditions | Yield |
---|---|
With dihydrogen peroxide at 30℃; for 5h; Green chemistry; | 85% |
Conditions | Yield |
---|---|
With methanol; sodium tetrahydroborate In tetrahydrofuran for 1h; Ambient temperature; | A 84% B 78% |
With sodium tetrahydroborate; nickel dichloride In diethylene glycol dimethyl ether for 1h; Product distribution; Ambient temperature; other symmetric and mixed anhydrides of carboxylic acids and carboxylic carbonic anhydrides; | A 78% B 80% |
Conditions | Yield |
---|---|
With tert-butyl alcohol In tetrahydrofuran electrolysis (Mg electrodes, LiClO4); | 82% |
(E)-1-ethoxyhept-1-ene
n-heptan1ol
Conditions | Yield |
---|---|
With chloro-trimethyl-silane; Benzyltriethylammonium borohydride; oxygen In dichloromethane at 0℃; for 6h; | 80% |
Conditions | Yield |
---|---|
With sodium periodate; C18H15ClFN2Ru(1+)*Cl(1-) In water; tert-butyl alcohol at 60℃; for 1h; Catalytic behavior; Schlenk technique; Inert atmosphere; | 80% |
Conditions | Yield |
---|---|
Stage #1: 1-Heptene With sodium tetrahydroborate; malonic acid In tetrahydrofuran at 60℃; for 5h; Stage #2: With sodium hydroxide; dihydrogen peroxide In tetrahydrofuran; water at 40 - 50℃; for 2h; Further stages.; | 79.5% |
Multi-step reaction with 2 steps 2: NaOH; H2O2 View Scheme |
Conditions | Yield |
---|---|
With 1-Phenylprop-1-yne; copper In tetrahydrofuran at 80℃; for 12h; | 76% |
Conditions | Yield |
---|---|
With oxygen; potassium carbonate In water at 50℃; for 24h; Green chemistry; | 100% |
With 4-methoxy-TEMPO; sodium hypochlorite; Aliquat 336; potassium bromide In dichloromethane; water at 0℃; for 0.0833333h; pH = 8.6; | 96% |
With dichloro(1,5-cyclooctadiene)ruthenium(II); C30H30N3P2(1+)*Cl(1-); potassium hydroxide In toluene at 120℃; for 24h; Time; Inert atmosphere; Schlenk technique; | 95% |
Conditions | Yield |
---|---|
potassium hydrogencarbonate at 180℃; for 1h; | 100% |
With potassium formate at 180℃; |
Conditions | Yield |
---|---|
potassium thioacyanate at 180℃; for 0.5h; | 100% |
With potassium thioacyanate at 180℃; |
Conditions | Yield |
---|---|
potassium phthalate at 180℃; for 0.3h; | 100% |
With potassium formate at 180℃; |
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Enzymatic reaction; | 100% |
With diphenylphosphinopolystyrene; diethylazodicarboxylate In tetrahydrofuran at 25℃; for 4h; | 90% |
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Enzymatic reaction; | 100% |
With diphenylphosphinopolystyrene; diethylazodicarboxylate In tetrahydrofuran at 25℃; for 4h; | 84% |
Conditions | Yield |
---|---|
K5 In acetonitrile at 20℃; for 0.416667h; | 100% |
With boron trifluoride diethyl etherate In ethyl acetate for 0.00138889h; | 100% |
With bismuth(lll) trifluoromethanesulfonate In acetonitrile at 20℃; for 0.0833333h; | 99% |
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Solvent; Enzymatic reaction; | 100% |
With 4-nitro-diphenylammonium triflate In toluene at 80℃; for 30h; | 95% |
With zirconocene bis(perfluorooctanesulfonate) trihydrate*(tetrahydrofuran) In neat (no solvent) at 80℃; Sealed tube; Green chemistry; chemoselective reaction; | 90% |
Conditions | Yield |
---|---|
With CuI; caesium carbonate In dodecane | 100% |
With CuI; caesium carbonate In dodecane; toluene | 68% |
With CuI; caesium carbonate In dodecane | 18% |
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Enzymatic reaction; | 100% |
With 25 wtpercent H3PO4/ZrO2-TiO2 at 130℃; for 1.75h; Neat (no solvent); chemoselective reaction; | 80% |
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Enzymatic reaction; | 100% |
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Enzymatic reaction; | 100% |
n-heptan1ol
4-trifluoromethylbenzoic acid
heptyl 4-(trifluoromethyl)benzoate
Conditions | Yield |
---|---|
With Candida antarctica lipase B immobilised in a macroporous DVB crosslinked polymer (Novozym 435) In cyclohexane at 80℃; for 24h; Enzymatic reaction; | 100% |
diethylphosphonoacetic acid
n-heptan1ol
heptyl 2-(diethoxyphosphoryl)acetate
Conditions | Yield |
---|---|
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine In ethyl acetate; toluene at 20℃; for 4h; Inert atmosphere; | 100% |
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine In tetrahydrofuran; ethyl acetate; toluene at 20℃; for 4h; Inert atmosphere; |
n-heptan1ol
3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-mannopyranosyl trichloroacetimidate
Conditions | Yield |
---|---|
Stage #1: n-heptan1ol; 3,4,6-tri-O-acetyl-2-deoxy-2-fluoro-α-D-mannopyranosyl trichloroacetimidate In dichloromethane at 20℃; for 0.5h; Molecular sieve; Inert atmosphere; Stage #2: With trimethylsilyl trifluoromethanesulfonate In dichloromethane at 20℃; for 2h; Molecular sieve; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With pyridine chromium peroxide In dichloromethane for 1.25h; Ambient temperature; | 99% |
With polymeric complex of oxodiperoxochromium(VI) compound and pyrazine (Pyz-CrO5)n In dichloromethane for 1.5h; Ambient temperature; | 99% |
With pyridine chromium peroxide In dichloromethane for 1.25h; Product distribution; Ambient temperature; effect of various chromium(VI) based oxidants; | 99% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; | 99% |
With triethylamine In dichloromethane at 0 - 20℃; | 99% |
With pyridine at 0℃; | |
With triethylamine In chloroform at 0 - 5℃; for 0.25h; |
Conditions | Yield |
---|---|
With bismuth(lll) trifluoromethanesulfonate at 20℃; for 0.5h; | 99% |
With K5 for 0.5h; Heating; | 98% |
With zinc(II) oxide for 3h; Reflux; | 73% |
Conditions | Yield |
---|---|
With iodine at 20℃; for 1h; Inert atmosphere; | 99% |
Stage #1: formic acid With silica gel at 20℃; for 0.0166667h; Stage #2: n-heptan1ol With silica gel at 110℃; for 0.05h; | 94% |
n-heptan1ol
di(n-butyl)tin oxide
1,1,3,3-tetra-n-butyl-1,3-diheptyloxydistannoxane
Conditions | Yield |
---|---|
at 150℃; for 8h; Inert atmosphere; Industry scale; | 99% |
at 150℃; under 760.051 Torr; for 8.5h; Inert atmosphere; Industry scale; | 99 %Spectr. |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 55℃; under 760.051 Torr; for 1h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With Co2Rh2 nanoparticles immobilized on charcoal at 140℃; for 24h; Schlenk technique; Inert atmosphere; Green chemistry; chemoselective reaction; | 99% |
Conditions | Yield |
---|---|
With Co2Rh2 nanoparticles immobilized on charcoal at 165℃; for 24h; Inert atmosphere; Schlenk technique; Green chemistry; chemoselective reaction; | 99% |
Conditions | Yield |
---|---|
With C26H42ClN2Ru(1+)*F6P(1-); potassium hydroxide In toluene at 120℃; for 3h; | 99% |
Conditions | Yield |
---|---|
With diphenylammonium trifluoromethanesulfonate In toluene at 80℃; for 6h; | 98.3% |
With sulfuric acid In toluene Fischer-Speier Esterification; Heating; | 76% |
With toluene-4-sulfonic acid In benzene Heating; |
Conditions | Yield |
---|---|
With dihydrogen peroxide; bromine In dichloromethane; water at 20℃; for 6h; Solvent; | 98% |
With N-Bromosuccinimide; L-proline In water at 20℃; for 1h; | 97% |
With sodium bromate; sulfuric acid; sodium bromide In water at 20℃; for 24h; | 97% |
Conditions | Yield |
---|---|
With tetrabutoxytitanium at 170 - 220℃; under 760.051 Torr; for 4.5h; Inert atmosphere; Large scale; | 98% |
With sulfuric acid at 150 - 200℃; |
n-heptan1ol
4-Chloro-2-(4-methyl-1-piperazinyl)quinazoline
4-Heptyloxy-2-(4-methyl-piperazin-1-yl)-quinazoline
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide | 98% |
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