manufacturer,good quality . Appearance:colorless liquid Package:200kg galvanized metal pail or 20T storage tank Application:used as Food addiitive , edible pigment , flavour and fragrance.also used in Eye drops solution. Transportation:by air or
Items Standard Result Appearance Colorless transparent liquid Complies Order Warm rose and honey
Cas:60-12-8
Min.Order:1 Kilogram
FOB Price: $7.0 / 15.0
Type:Manufacturers
inquiryWelcome 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
Cas:60-12-8
Min.Order:1 Kilogram
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inquiryProduct Description
Cas:60-12-8
Min.Order:1 Kilogram
FOB Price: $5.0 / 30.0
Type:Lab/Research institutions
inquiryhebei yanxi chemical co., LTD who registered capital of 10 million yuan, nearly to $2 million, we have a pharmaceutical raw materials factory production of pharmaceutical raw materials, and a reagent r&d center, and we do research and developm
Cas:60-12-8
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Type:Manufacturers
inquiryPhenethyl alcohol CAS RN 60-12-8;1321-27-3 EINECS 200-456-2 Molecular formula C8H10O Molecular weight 122.16 Structural formula
Cas:60-12-8
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Type:Manufacturers
inquiryThe 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
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Cas:60-12-8
Min.Order:1 Gram
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Type:Manufacturers
inquiryShanghai 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:60-12-8
Min.Order:1 Kilogram
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Type:Manufacturers
inquiryColorcom is a global leader in industrial chemical manufacturing and is continuously innovating and transforming to exceed client expectations and industry standards. Colorcom prides itself on superior customer and technical focus, while focusing on
Dayangchem’s 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. DayangChem can provide different quantiti
Cas:60-12-8
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Type:Lab/Research institutions
inquiryOur 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
Cas:60-12-8
Min.Order:5 Kiloliter
FOB Price: $1.2 / 5.0
Type:Manufacturers
inquiryOur company was built in 2009 with an ISO certificate.In the past 5 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.O
Cas:60-12-8
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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
WITH 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
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Type:Trading Company
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Cas:60-12-8
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Type:Trading Company
inquiryName: Phenethyl alcohol Synonyms: 1-Phenyl-2-Ethanol CAS:60-12-8 MF: C8H10O Appearance:Colorless transparent liquid, Storage: Preserve in well-closed, light-resistant and airtight containers. Package: 25kgs/drum Application:Daily Flavor, In
We are leading fine chemicals supplier in China and Our main business covers the fields below: 1.Noble Metal Catalysts (Pt.Pd...) 2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...) 3.OLED interme
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inquiry1. Guaranteed purity; 2. Large quantity in stock; 3. Largest manufacturer; 4. Best service after shipment with email; 5. High quality & competitive price; Appearance:White Crystalline Powder Storage:Store in sealed conta
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Min.Order:10 Gram
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Type:Other
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
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Type:Lab/Research institutions
inquiryPhenethyl alcohol CAS: 60-12-8 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 intermedi
Cas:60-12-8
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
Cas:60-12-8
Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiryHubei CuiRan Biotechnology Co., Ltd is a leading company in the research, development, manufacture and marketing of High Quality Phytochemicals and Extracts(especially Active Ingredients from Traditional Chinese Medicine,Traditional Chinese Medicine)
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Cas:60-12-8
Min.Order:10 Gram
Negotiable
Type:Trading Company
inquiry1. Timely and efficient service to ensure communication with customers 2. Produce products of different specifications and sizes according to your requirements. 3. Quality procedures and standards recognized by SGS. Advanced plant equipment ensures s
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Min.Order:1 Kilogram
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Type:Lab/Research institutions
inquiry1) For products exported we can offer COA Certificate and official PI. 2) We are manufacturer with own lab and factory, can provide high quality products with factory price. 3) Products can be sent out in 24 hours after payment. Tracking number avai
Cas:60-12-8
Min.Order:100 Kilogram
Negotiable
Type:Trading Company
inquiryBest 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
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Cas:60-12-8
Min.Order:0 Metric Ton
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Type:Lab/Research institutions
inquiryCompany Introduction 1. Established in 2005, with two independent business divisions: Fine chemicals division; Pharmaceutical division. 2. Main product: Optical brightener Textile auxiliary Dye stuff Pigments
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
Conditions | Yield |
---|---|
With morpholine-borane; boron trifluoride diethyl etherate In diethyl ether for 2h; Product distribution; Ambient temperature; | 100% |
With ammonium formate; palladium on activated charcoal In methanol for 2h; Heating; | 100% |
With hydrogen In methanol at 25℃; under 750.075 Torr; Reagent/catalyst; Flow reactor; regioselective reaction; | 100% |
trimethyl(phenethyloxy)silane
2-phenylethanol
Conditions | Yield |
---|---|
With Dowex 1-X8 In ethanol for 8h; Ambient temperature; | 100% |
With bismuth(lll) trifluoromethanesulfonate In methanol at 20℃; for 0.0166667h; | 98% |
With methanol; 1,3-disulfonic acid imidazolium hydrogen sulfate at 20℃; for 0.0833333h; Green chemistry; | 98% |
1-tert-butyldimethylsilyloxy-2-phenylethane
2-phenylethanol
Conditions | Yield |
---|---|
With iron(III) chloride In methanol at 23℃; for 3.5h; | 100% |
With water; scandium tris(trifluoromethanesulfonate) In acetonitrile for 1h; Ambient temperature; | 98% |
sulfonic acid functionalized nanoporous silica In methanol at 35℃; for 1.5h; | 98% |
Conditions | Yield |
---|---|
With potassium tert-butylate; hydrogen In ethanol at 40℃; under 7600.51 Torr; for 19h; Solvent; Autoclave; Inert atmosphere; | 100% |
With magnesium sulfate In tetrahydrofuran; dichloromethane | 92% |
With magnesium sulfate In tetrahydrofuran; dichloromethane | 92% |
Conditions | Yield |
---|---|
With phosphate buffer; Phenyl acetate In diethyl ether for 2.75h; Ambient temperature; pig liver acetone powder; | A 18% B 100% |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; silica gel In hexane for 3h; Heating; | 100% |
With methanol; sodium tetrahydroborate In diethyl ether at 20℃; for 38h; Reduction; | 96% |
With sodium tetrahydroborate In diethylene glycol dimethyl ether at 104℃; | 95% |
1-(triethylsiloxy)-2-phenylethane
2-phenylethanol
Conditions | Yield |
---|---|
With iron(III) chloride In methanol at 23℃; for 0.0833333h; | 100% |
With methanol; trimethylsilyl bromide at 20℃; for 0.166667h; chemoselective reaction; | 98% |
With Selectfluor In acetonitrile at 150℃; for 0.05h; Microwave irradiation; | 82% |
With iron(III) p-toluenesulfonate hexahydrate In methanol at 20℃; for 0.333333h; | 80% |
With hydrogenchloride In methanol at 20℃; for 16h; |
C24H20O3
2-phenylethanol
Conditions | Yield |
---|---|
With (triphenylphosphine)gold(I) chloride; silver trifluoromethanesulfonate In ethanol; benzene at 20℃; for 0.3h; | 100% |
allyl 2-phenylethyl carbonate
2-phenylethanol
Conditions | Yield |
---|---|
[RuCp(η3-C3H5)(QA)]PF6, QA=quinaldic acid In methanol at 30℃; for 0.5h; | 99% |
With Fe3O4@SiO2-[(4-(5-O3Si-pentylcarbamoyl)-2-pyridinecarboxylato)CpRu(η3-C3H5)]PF6 In methanol at 30℃; for 2h; Inert atmosphere; chemoselective reaction; | 99.9% |
[RuCp(η3-C3H5)(QA)]PF6, QA=quinaldic acid In methanol at 30℃; for 0.5h; Product distribution; Further Variations:; Solvents; | 99 % Spectr. |
ethylbenzene
A
4-Ethylphenol
B
1-Phenylethanol
C
2-phenylethanol
Conditions | Yield |
---|---|
With rabbit liver microsomal cytochrome P-450 In water at 25℃; for 12h; | A 0.13% B 99.8% C 0.08% |
Conditions | Yield |
---|---|
With [carbonylchlorohydrido{bis[2-(diphenylphosphinomethyl)ethyl]amino}ethylamino] ruthenium(II); potassium tert-butylate; hydrogen In toluene at 75℃; under 37503.8 Torr; for 24h; Catalytic behavior; Pressure; Temperature; Reagent/catalyst; regioselective reaction; | A 99% B n/a |
With lithium triethylborohydride In tetrahydrofuran at 0℃; for 0.0833333h; Product distribution; | A 97% B 3% |
With Li(1+)*C12H28AlO3(1-) In tetrahydrofuran; hexane at 0℃; for 0.17h; Yields of byproduct given; | A 95% B n/a |
Conditions | Yield |
---|---|
With N,N,N,N,N,N-hexamethylphosphoric triamide; tri-n-butyl-tin hydride for 2h; Product distribution; Ambient temperature; different aldehydes, reagents, reaction temperature and time; | 99% |
With N,N,N,N,N,N-hexamethylphosphoric triamide; tri-n-butyl-tin hydride for 2h; Ambient temperature; | 99% |
With hydrogen In water at 60℃; under 22502.3 Torr; for 0.00611111h; Flow reactor; Green chemistry; chemoselective reaction; | 99% |
Conditions | Yield |
---|---|
With C30H34Cl2N2P2Ru; potassium methanolate; hydrogen In tetrahydrofuran at 100℃; under 38002.6 - 76005.1 Torr; for 5h; Glovebox; Autoclave; | 99% |
95% | |
With lithium borohydride In diethyl ether; toluene at 100℃; for 1h; | 92% |
2-(2-propenyloxy)ethylbenzene
2-phenylethanol
Conditions | Yield |
---|---|
With quinoline-2-carboxylic acid; cyclopentadienylruthenium(II) trisacetonitrile hexafluorophosphate In methanol at 30℃; for 3h; | 99% |
[RuCp(η3-C3H5)(QA)]PF6, QA=quinaldic acid In methanol at 30℃; for 3h; | 99% |
quinoline-2-carboxylic acid; cyclopentadienylruthenium(II) trisacetonitrile hexafluorophosphate In methanol; dichloromethane at 30℃; for 0.5h; Conversion of starting material; | 99% |
Conditions | Yield |
---|---|
With tri-n-butyl-tin hydride; hafnium tetrachloride In tetrahydrofuran at -20℃; for 3h; Inert atmosphere; | 99% |
With (Ppyz)Zr(BH4)2Cl2 In diethyl ether for 8h; Heating; | 92% |
With phenylsilane; potassium tert-butylate; water; sodium triethylborohydride; cobalt(II) chloride In 1,4-dioxane; toluene at 60℃; for 15h; Inert atmosphere; Glovebox; Schlenk technique; | 84% |
2-phenylethanol
Conditions | Yield |
---|---|
With Oxone; water In acetone at 20℃; for 0.0333333h; | 99% |
Conditions | Yield |
---|---|
With zinc(II) tetrahydroborate; N,N,N,N,-tetramethylethylenediamine In diethyl ether at 0℃; for 0.5h; | 98% |
With methyltriphenylphosphonium tetrahydroborate In dichloromethane Reduction; | 98% |
With Zr(BH4)2Cl2(dabco)2 In tetrahydrofuran for 1.2h; Heating; | 98% |
Conditions | Yield |
---|---|
With bismuth(lll) trifluoromethanesulfonate In methanol for 0.05h; Heating; | 98% |
With dimethylbromosulphonium bromide In methanol; dichloromethane at 20℃; for 0.416667h; | 97% |
With trichloroisocyanuric acid In methanol at 20℃; for 5h; | 96% |
Conditions | Yield |
---|---|
Stage #1: isopropyl phenylacetate With diethylzinc; lithium chloride In tetrahydrofuran; hexane at 20℃; for 6h; Inert atmosphere; Stage #2: With sodium hydroxide In tetrahydrofuran; hexane; water at 20℃; for 8h; Catalytic behavior; Concentration; Time; Inert atmosphere; chemoselective reaction; | 98% |
With phenylsilane; potassium tert-butylate; water; sodium triethylborohydride; cobalt(II) chloride In 1,4-dioxane; toluene at 60℃; for 15h; Inert atmosphere; Glovebox; Schlenk technique; | 93% |
Stage #1: isopropyl phenylacetate With diethoxymethylane; zinc diacetate In tetrahydrofuran at 65℃; for 24h; Inert atmosphere; Stage #2: With methanol; potassium hydroxide chemoselective reaction; | 98 %Chromat. |
Stage #1: isopropyl phenylacetate With iron (II) stearate; ethylenediamine In toluene at 20℃; for 0.0833333h; Inert atmosphere; Schlenk technique; Stage #2: In toluene at 100℃; for 20h; Inert atmosphere; Schlenk technique; | 71 %Chromat. |
With 1,1'-methylene-bis(3-benzyl-1H-imidazol-3-ium) diiodide; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; potassium tert-butylate; hydrogen In 1,4-dioxane at 100℃; under 37503.8 Torr; for 6h; | 50 %Chromat. |
allyl 2-phenylethyl carbonate
2-propanethiol
A
allylisopropyl sulfide
B
carbon dioxide
C
2-phenylethanol
Conditions | Yield |
---|---|
With [Bu4N][Fe(CO)3(NO)]; tris(2,4,6-trimethylphenyl)phosphine In ethanol at 40℃; Inert atmosphere; | A n/a B n/a C 98% |
(2-phenylethyl)boronic acid
2-phenylethanol
Conditions | Yield |
---|---|
With pyrene-1,6-dione; oxygen; isopropyl alcohol at 20℃; under 760.051 Torr; for 40h; Irradiation; Green chemistry; | 98% |
With rose bengal; triethylamine In ethanol at 25℃; for 12h; Schlenk technique; Irradiation; | 97% |
With 2,5-dimethylfuran; zinc(II) phthalocyanine; oxygen In tetrahydrofuran at 25℃; under 760.051 Torr; for 2h; Time; Irradiation; Sealed tube; Schlenk technique; | 95% |
(+/-)-2-(3-cyclohexenyl)ethanol
2-phenylethanol
Conditions | Yield |
---|---|
With hydrogen at 250℃; under 750.075 Torr; Reagent/catalyst; Green chemistry; | 97.92% |
Conditions | Yield |
---|---|
With [Zn(BH4)2(py)] In tetrahydrofuran for 1.5h; Heating; | 97% |
With zinc(II) tetrahydroborate In tetrahydrofuran for 3h; Heating; | 95% |
With borane-THF In tetrahydrofuran for 3.25h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With iron(III) sulfate; water In toluene at 110℃; for 1h; Ionic liquid; | 97% |
With sodium carbonate at 160 - 165℃; | |
With sodium carbonate at 175℃; |
Conditions | Yield |
---|---|
With methanol; sodium tetrahydroborate In tetrahydrofuran for 1h; Ambient temperature; | A 94% B 97% |
N-(4-Phenethyloxymethyl-phenyl)-acetamide
2-phenylethanol
Conditions | Yield |
---|---|
With 2,3-dicyano-5,6-dichloro-p-benzoquinone | 97% |
(2-(methoxymethoxy)ethyl)benzene
2-phenylethanol
Conditions | Yield |
---|---|
phosphotungstic acid In ethanol for 3h; Heating; | 97% |
With 1-methylimidazole hydrogen sulfate at 120℃; for 0.025h; Microwave irradiation; chemoselective reaction; | 95% |
With 1-thiopropane; zinc dibromide In dichloromethane at 20℃; for 0.1h; Inert atmosphere; | 90% |
Conditions | Yield |
---|---|
With [2,2]bipyridinyl; formic acid; (η5-cyclopentadienyl) (η6-naphthalene)ruthenium hexafluorophosphate; water In tetrahydrofuran at 55℃; for 48h; | 97% |
With 1-hydroxytetraphenylcyclopentadienyl(tetraphenyl-2,4-cyclopentadien-1-one)-μ-hydrotetracarbonyldiruthenium(II); Ru(Cp)(PPh2PytBu)2(MeCN)PF6; water In isopropyl alcohol at 70℃; for 48h; Concentration; Reagent/catalyst; Inert atmosphere; regioselective reaction; | 90% |
With formic acid; F6P(1-)*C16H22N3Ru(1+); water In 1-methyl-pyrrolidin-2-one at 25℃; for 48h; Inert atmosphere; Sealed tube; | 83% |
Multi-step reaction with 2 steps 1: cyclopentadienylruthenium(II) trisacetonitrile hexafluorophosphate; [2,2]bipyridinyl; formic acid / water; 1-methyl-pyrrolidin-2-one / 24 h / 25 °C / Inert atmosphere; Sealed tube 2: N1,N1-dimethyl-N2-(pyridin-2-ylmethylene)ethane-1,2-diamine; cyclopentadienylruthenium(II) trisacetonitrile hexafluorophosphate; formic acid; water / 1-methyl-pyrrolidin-2-one / 24 h / 25 °C / Inert atmosphere; Sealed tube View Scheme |
Conditions | Yield |
---|---|
With water at 20℃; for 0.166667h; | 96% |
With methanol; potassium permanganate at 25℃; chemoselective reaction; | 92% |
With 2,2-dibutyl-1,3,2-dioxastannane; cesium fluoride In N,N-dimethyl-formamide at 20℃; for 0.5h; | 85% |
2-phenylethanol
2-phenethyl iodide
Conditions | Yield |
---|---|
With 1H-imidazole; iodine; triphenylphosphine In diethyl ether at 0℃; for 1h; | 100% |
With trimethylsilylphosphate; sodium iodide for 10h; Ambient temperature; | 98% |
With N-iodosaccharine; triphenylphosphine In dichloromethane at 20℃; for 0.5h; | 95% |
Conditions | Yield |
---|---|
With magnesium(II) perchlorate at 20℃; for 0.25h; | 100% |
Stage #1: acetic anhydride With molybdenium(VI) dioxodichloride In dichloromethane at 20℃; for 0.5h; Stage #2: 2-phenylethanol In dichloromethane at 20℃; for 0.1h; | 100% |
With boron trifluoride diethyl etherate In ethyl acetate for 0.00138889h; | 100% |
2-phenylethanol
trichloroacetonitrile
β-phenylethyl trichloroacetimidate
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene In dichloromethane | 100% |
With sodium | |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In dichloromethane at 20℃; |
Conditions | Yield |
---|---|
With TiO(acac)2 In xylene for 15h; Heating; | 100% |
With iron(III)-acetylacetonate In 5,5-dimethyl-1,3-cyclohexadiene for 15h; Inert atmosphere; Reflux; | 97% |
With 4-nitro-diphenylammonium triflate In toluene at 80℃; for 30h; | 95% |
2-phenylethanol
N-(tert-butyloxycarbonyl)(2-trimethylsilylethyl)sulfonamide
Conditions | Yield |
---|---|
With triphenylphosphine; diethylazodicarboxylate In tetrahydrofuran at 0℃; for 0.0833333h; | 100% |
Conditions | Yield |
---|---|
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium hypochlorite; sodium chlorite In acetonitrile at 35℃; pH 6.7; | 100% |
With sodium hypochlorite; sodium chlorite; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical In aq. phosphate buffer; water; acetonitrile at 35℃; pH=6.7; Green chemistry; | 100% |
With oxygen; sodium hydroxide In water at 90℃; for 18h; Catalytic behavior; | 100% |
carbon disulfide
2-phenylethanol
methyl iodide
S-methyl O-phenylethyl carbonodithioate
Conditions | Yield |
---|---|
Stage #1: 2-phenylethanol With sodium hydride In tetrahydrofuran; mineral oil for 0.333333h; Stage #2: carbon disulfide In tetrahydrofuran; mineral oil at 20℃; for 0.333333h; Stage #3: methyl iodide In tetrahydrofuran; mineral oil for 0.333333h; | 100% |
Stage #1: carbon disulfide; 2-phenylethanol With 1H-imidazole; sodium hydride In tetrahydrofuran at 20℃; for 0.5h; Stage #2: methyl iodide In tetrahydrofuran at 20℃; for 0.5h; | 95% |
With sodium hydroxide; tetrabutylammomium bromide In water | 75% |
Yield given. Multistep reaction; |
Conditions | Yield |
---|---|
at 20℃; for 0.0833333h; Neat (no solvent); | 100% |
With lanthanum(III) nitrate at 20℃; for 0.166667h; | 96% |
With pyridine In dichloromethane at 25℃; for 5h; Acylation; | |
With picoline In dichloromethane for 1h; Reflux; | |
Stage #1: 2-phenylethanol With bis(cyclopentadienyl)titanium dichloride; manganese; diiodomethane In tetrahydrofuran at 20℃; for 2.5h; Inert atmosphere; Stage #2: pivaloyl chloride In tetrahydrofuran at 20℃; for 1.5h; Solvent; Inert atmosphere; |
3,4-dihydro-2H-pyran
2-phenylethanol
2-(2-phenylethoxy)tetrahydro-2H-pyran
Conditions | Yield |
---|---|
With H6P2W18O62 In toluene at 20℃; for 2h; | 100% |
With phosphotungstic acid In toluene at 20℃; for 1h; | 100% |
With iron(III) sulfate at 20℃; for 1h; | 98% |
2-phenylethanol
4-carboxymethoxy-benzoic acid
Conditions | Yield |
---|---|
With [Cl(C6F13C2H4)2SnOSn(C2H4C6F13)2Cl]2 In various solvent(s) at 150℃; for 16h; | 100% |
Conditions | Yield |
---|---|
With [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold (I) at 150℃; for 0.5h; Kinetics; Inert atmosphere; Microwave irradiation; | 100% |
With (triphenylphosphine)gold(I) chloride at 150℃; for 1.5h; Microwave irradiation; Green chemistry; | 96% |
With n-butyllithium; 2,3,5,6-tetrafluoro-1,4-benzoquinone; chloro-diphenylphosphine In dichloromethane at 20℃; for 3h; Product distribution; Further Variations:; Reagents; | 72% |
Conditions | Yield |
---|---|
Stage #1: butanoic acid anhydride With molybdenium(VI) dioxodichloride In dichloromethane at 20℃; for 0.5h; Stage #2: 2-phenylethanol In dichloromethane at 20℃; for 0.15h; | 100% |
With iron(III) p-toluenesulfonate hexahydrate In neat (no solvent) at 20℃; for 1h; | 85% |
di-n-butyloxymethane
2-phenylethanol
formaldehyde-(butyl-phenethyl-acetal)
Conditions | Yield |
---|---|
With Nafion-H SAC-13 silica nanocomposite at 100℃; | 100% |
2-phenylethanol
chloro-diphenylphosphine
2-phenylethyl diphenylphosphinite
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran; hexane at 0℃; for 1h; | 100% |
With n-butyllithium In tetrahydrofuran at 0℃; for 1h; | |
With triethylamine In dichloromethane at 20℃; for 2h; Inert atmosphere; | |
Stage #1: 2-phenylethanol With n-butyllithium In tetrahydrofuran at 0℃; for 1h; Inert atmosphere; Schlenk technique; Stage #2: chloro-diphenylphosphine In tetrahydrofuran at 20℃; for 1h; Inert atmosphere; Schlenk technique; |
Conditions | Yield |
---|---|
at 50℃; for 120h; | 100% |
Stage #1: 2-phenylethanol; caffeic acid at 20℃; for 0.25h; Molecular sieve; Ionic liquid; Inert atmosphere; Stage #2: With Tocopherol at 130℃; under 760.051 Torr; for 0.15h; Solvent; Reagent/catalyst; Temperature; Molecular sieve; Ionic liquid; Inert atmosphere; Microwave irradiation; | 95% |
In benzene for 84h; Heating; Dean-Stark trap; | 40% |
2-phenylethanol
Conditions | Yield |
---|---|
With 2,6-dimethylpyridine; diazaphospholidinium-based reagent In acetonitrile at 20℃; for 0.166667h; | 100% |
Conditions | Yield |
---|---|
With 1,1'-bis-(diphenylphosphino)ferrocene; 3 A molecular sieve; potassium carbonate; [Ru(p-cumene)Cl2]2 In toluene at 110℃; for 24h; Product distribution; Further Variations:; Catalysts; | 100% |
With 1,1'-bis(diphenylphosphino)ferrocene; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; potassium carbonate In toluene at 20℃; for 24.1667h; Inert atmosphere; Molecular sieve; Reflux; | 88% |
With C61H45N3OP2RuS; potassium hydroxide In toluene at 110℃; for 12h; Schlenk technique; | 79% |
Stage #1: 2-phenylethanol With 1,1'-bis-(diphenylphosphino)ferrocene; [RuCl2(p-cymene)(3-INC5H4)] In toluene for 0.166667h; Reflux; Stage #2: tert-butylamine In toluene; acetonitrile for 24h; Reagent/catalyst; Reflux; | |
Stage #1: 2-phenylethanol With [bis((μ-chloro)chloro(η6-phenylacetic acid)ruthenium(II))] In toluene at 110℃; for 0.166667h; Reflux; Stage #2: tert-butylamine In toluene; acetonitrile at 110℃; for 24h; Catalytic behavior; Reagent/catalyst; Time; Reflux; |
2-phenylethanol
ethenyltrimethylsilane
A
ethene
B
trimethyl(phenethyloxy)silane
Conditions | Yield |
---|---|
hydrogenchloride; chlorobis(ethylene)rhodium(I) dimer In 1,4-dioxane; chloroform at 20℃; for 2h; Product distribution / selectivity; | A n/a B 100% |
chlorobis(cyclooctene)rhodium(I) dimer In toluene at 70℃; for 3h; Product distribution / selectivity; | A n/a B 100% |
hydrogenchloride; chlorobis(cyclooctene)rhodium(I) dimer In 1,4-dioxane; chloroform at 20℃; for 2h; Product distribution / selectivity; | A n/a B 96% |
Conditions | Yield |
---|---|
Stage #1: acetic anhydride; TiO(OTf)2 In dichloromethane at 20℃; for 0.5h; Stage #2: 2-phenylethanol In dichloromethane at 20℃; for 0.3h; Product distribution / selectivity; | 100% |
Stage #1: acetic anhydride; bis(tetrahydrofurane)oxovanadium(IV) dichloride In dichloromethane at 20℃; for 0.5h; Stage #2: 2-phenylethanol In dichloromethane at 20℃; for 12h; Product distribution / selectivity; | 99% |
Stage #1: acetic anhydride; bis(acetylacetonato)dioxidomolybdenum(VI) In dichloromethane at 20℃; for 0.5h; Stage #2: 2-phenylethanol In dichloromethane at 20℃; for 16h; Product distribution / selectivity; | 98% |
4-[(6,7-dimethoxy-4-quinolyl)oxy]-2,5-dimethylaniline
bis(trichloromethyl) carbonate
2-phenylethanol
sodium hydrogencarbonate
Conditions | Yield |
---|---|
With triethylamine In methanol; dichloromethane; chloroform; toluene | 100% |
2-phenylethanol
Conditions | Yield |
---|---|
100% |
Conditions | Yield |
---|---|
With cyclooctadiene ruthenium(II) dichloride; potassium tert-butylate; 1,3-diisopropyl-1H-imidazol-3-ium chloride; tricyclopentylphosphonium tetrafluoroborate In toluene for 24h; Inert atmosphere; Reflux; | 100% |
With dichloro(1,5-cyclooctadiene)ruthenium(II); potassium tert-butylate; 1,3-diisopropyl-1H-imidazol-3-ium chloride; tricyclopentylphosphonium tetrafluoroborate In toluene at 110℃; for 24h; Inert atmosphere; | 100% |
With pyridine; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; sodium hydride; 1,3-di(propan-2-yl)-1H-imidazol-3-ium bromide In toluene for 36h; Inert atmosphere; Reflux; | 98% |
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