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Cas:2305-13-7
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inquiryDIHYDROCONIFERYL ALCOHOL CAS:2305-13-7 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 i
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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
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inquiryHenan 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
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inquiryJ&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
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inquiryZibo 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
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inquiryDIHYDROCONIFERYL ALCOHOL Basic information Product Name: DIHYDROCONIFERYL ALCOHOL Synonyms: 3-(4-HYDROXY-3-METHO
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inquiryProduct 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,
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inquiryStock products, own laboratory Package:Grams, Kilograms Application:For R&D Transportation:According to customer request Port:Shanghai
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inquiryhigh purity,in stock Package:25kg/drum,or as per customers'demand Application:API,Pharmaceutical intermediates Transportation:air,sea,courier
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inquiryAcmec 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
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inquiryhigh 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
Hunan chemfish Pharmaceutical co.,Ltd.located in Lugu High-tech industral park ,Hunan province . with its own R&D center and more than 10000㎡manufacture plant . Chemfish owns 40 reactors from 1000L to 8000L. With complete auxiliary equipment as
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
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inquiry3-(4-Hydroxy-3-methoxyphenyl)-1-propanol cas 2305-13-7Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
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inquiryfactory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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inquirygood quality, competitive price, thoughtful after sale serviceAppearance:white powder Storage:Keep it in dry,shady and cool place Package:5mg Application:Pharma;Industry;Agricultural;chemical reaserch Transportation:by express or by sea Port:Any port
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factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
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inquiryChangzhou Extraordinary Pharmatech co., LTD. As a leading chemical manufacturer and supplier in China.DAS authentication is passed.We can provide the popular precursor chemicals, we have our own strong R & D team, have our own laboratories and fa
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United Scientific Company Located in Shanghai of China , is a competitive player in the global specialty and fine chemical market. Fenghua has both the expertise and flexibility to produce a wide range of chemicals. Focusing on developing the innovat
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inquirytrans-coniferyl aldehyde
A
3-Guaiacylpropanol
B
coniferal alcohol
Conditions | Yield |
---|---|
With sodium tetrahydroborate In ethyl acetate for 1h; Ambient temperature; | A 1% B 99% |
guaiacylglycerol-β-guaiacyl ether
A
2-methoxy-4-n-propylphenol
B
3-Guaiacylpropanol
C
2-methoxy-phenol
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen; zinc(II) acetate dihydrate In methanol at 225℃; under 26618.1 Torr; Catalytic behavior; | A 69% B 20% C 98% |
With hydrogen In methanol at 260℃; under 22502.3 Torr; for 12h; Catalytic behavior; Temperature; Time; | A 43 %Chromat. B 11 %Chromat. C 71 %Chromat. |
With hydrogen In methanol at 220℃; under 22502.3 Torr; for 8h; Catalytic behavior; Temperature; | A 11 %Chromat. B 44 %Chromat. C 76 %Chromat. |
guaiacylglycerol-β-guaiacyl ether
A
3-Guaiacylpropanol
B
2-methoxy-phenol
Conditions | Yield |
---|---|
With formic acid In water at 120℃; for 3h; Green chemistry; | A 93% B 95% |
With palladium 10% on activated carbon; hydrogen In methanol at 225℃; under 26618.1 Torr; Catalytic behavior; | A 74% B 74% |
With 10% nickel/activated carbon; hydrogen In 1,4-dioxane at 150℃; under 15001.5 Torr; for 2h; Autoclave; | A 7.7% B 6.4% |
coniferal alcohol
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With ferrous ammonium sulphate hexahydrate; isopropyl β-D-thiogalactopyranoside In aq. phosphate buffer at 37℃; for 48h; | 91% |
With hydrogen; palladium on activated charcoal In methanol at 20℃; for 4h; | 90% |
With hydrogen; palladium on activated charcoal In ethyl acetate for 3h; | 55 mg |
methyl 3-(4-hydroxy-3-methoxyphenyl)propanoate
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With sodium tetrahydroborate In water for 8h; Ambient temperature; | 90% |
With lithium aluminium tetrahydride In diethyl ether | |
With lithium borohydride In diethyl ether; toluene for 0.25h; Heating; | |
With lithium aluminium tetrahydride Reduction; |
4-allylguaiacol
A
3-Guaiacylpropanol
B
1-(4-hydroxy-3-methoxyphenyl)-2-propanol
Conditions | Yield |
---|---|
Stage #1: 4-allylguaiacol With dimethylsulfide borane complex In tetrahydrofuran Stage #2: With sodium hydroxide; dihydrogen peroxide In tetrahydrofuran | A 84% B n/a |
Stage #1: 4-allylguaiacol With dimethylsulfide borane complex In tetrahydrofuran at 0 - 20℃; for 2h; Stage #2: With dihydrogen peroxide; sodium hydroxide In tetrahydrofuran at 0 - 20℃; for 1h; Inert atmosphere; | A 80% B n/a |
With sodium hydroxide; tetrabutylammonium boranate; dihydrogen peroxide; methyl iodide 1.) CH2Cl2, reflux, 30 min, 2.) 1.5 h; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts; |
Conditions | Yield |
---|---|
With whole cell cultures of dichomitus albidofuscus at 24℃; for 72h; Darkness; Microbiological reaction; | 77% |
Multi-step reaction with 2 steps 1: LiAlH4 / tetrahydrofuran / 1 h / -30 °C 2: H2 / 10percent Pd-charcoal / methanol / 2 h / 1810.02 Torr View Scheme | |
With D-Glucose; Escherichia coli endogenous alcohol dehydrogenase; Segniliparus rugosus carboxylic acid reductase; dimethyl sulfoxide; magnesium chloride In aq. phosphate buffer at 30℃; for 18h; pH=7.5; Enzymatic reaction; |
guaiacylglycerol-β-guaiacyl ether
A
3-Guaiacylpropanol
B
3-Hydroxy-1-methoxy-2-(2-methoxy-phenoxy)-1-(4-hydroxy-3-methoxy-phenyl)-propan
C
2-methoxy-phenol
Conditions | Yield |
---|---|
With 10% nickel/activated carbon; hydrogen In methanol at 120℃; under 15001.5 Torr; for 2h; Time; Autoclave; | A 7.4% B 72.8% C 9.2% |
coniferaldehyde
A
3-Guaiacylpropanol
B
3-(3'-methoxy-4'-hydroxyphenyl)propionaldehyde
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen for 2h; | A 70.4% B 11.9% |
1,3-dihydroxy-1-(4-O-benzyl-3-methoxyphenyl)propane
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With hydrogenchloride In water | 45% |
(E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid
A
trans-coniferyl aldehyde
B
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With D-glucose In aq. phosphate buffer at 30℃; for 16h; pH=8; Enzymatic reaction; | A n/a B 22% |
ethanol
ethyl 3-(4-hydroxy-3-methoxyphenyl)propanoate
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With sodium anschliessendes Kochen mit Wasser; |
Conditions | Yield |
---|---|
With ethanol; nickel Hydrogenation; | |
With tetrahydrofuran; palladium Hydrogenation; | |
With hydroxide; hydrogen; nickel In ethanol | |
With hydrogen; palladium on activated charcoal In methanol under 1810.02 Torr; for 2h; |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride | |
Multi-step reaction with 2 steps 1: 98 percent H2SO4 2: LiAlH4 / diethyl ether View Scheme |
ethyl 3-(4-hydroxy-3-methoxyphenyl)propanoate
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With ethanol; sodium |
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With sodium hydroxide; nickel at 165℃; under 154457 Torr; Hydrogenation; |
3.6-Bis-hydroxymethyl-2.5-bis-<4-hydroxy-3-methoxy-phenyl>-1.4-dithian
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With sodium hydroxide; nickel In ethylene glycol |
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With sodium hydroxide at 170℃; |
1-(4-hydroxy-3-methoxyphenyl)-2-<4-(ω-hydroxypropyl-2-methoxy)-phenoxy>-propane-1,3-diol
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With sodium sulfide; sodium hydroxide at 135℃; |
Conditions | Yield |
---|---|
With sodium hydroxide; dimethylsulfide; borane; dihydrogen peroxide other reagents: borane/THF, 9-borabicyclo<3.3.1>nonane; Multistep reaction; |
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With Trimethyl borate; sodium |
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With ethanol; hydrogen; nickel at 170℃; under 154457 Torr; |
diethyl ether
ω-hydroxypropioguaiacone diacetate
A
3-Guaiacylpropanol
B
3-hydroxy-3-(4-hydroxy-3-methoxyphenyl)-1-propanol
bis-[3-(4-hydroxy-3-methoxy-phenyl)-3-oxo-propyl]-ether
A
2-methoxy-4-n-propylphenol
B
3-Guaiacylpropanol
Conditions | Yield |
---|---|
at 165℃; under 154457 Torr; Hydrogenation; |
A
carbon dioxide
B
carbon monoxide
C
3-Guaiacylpropanol
D
coniferal alcohol
Conditions | Yield |
---|---|
With air Oxidation; Formation of xenobiotics; Further byproducts given; |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: H+ 2: H2 / 10 percent Pd/C 3: LiAlH4 View Scheme | |
Multi-step reaction with 3 steps 1: aq. HCl / 6 h / Heating 2: H2 / 10percent Pd/C / methanol / 0.5 h / 760 Torr / Ambient temperature 3: LiBH4 / diethyl ether; toluene / 0.25 h / Heating View Scheme | |
Multi-step reaction with 3 steps 1: sulfuric acid / 12 h / Reflux; Inert atmosphere 2: diisobutylaluminium hydride / dichloromethane; hexane / 3 h / -78 °C / Inert atmosphere 3: ferrous ammonium sulphate hexahydrate; isopropyl β-D-thiogalactopyranoside / aq. phosphate buffer / 48 h / 37 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: H2 / 10 percent Pd/C 2: LiAlH4 View Scheme | |
Multi-step reaction with 2 steps 1: H2 / 10percent Pd/C / methanol / 0.5 h / 760 Torr / Ambient temperature 2: LiBH4 / diethyl ether; toluene / 0.25 h / Heating View Scheme |
A
2-methoxy-4-n-propylphenol
B
4-n-propylsyringol
C
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With rhodium on carbon; hydrogen In water at 199.84℃; under 25858.1 Torr; for 1h; Autoclave; | |
With rhodium on carbon; hydrogen In water at 199.84℃; under 25858.1 Torr; for 4h; Autoclave; |
3-Guaiacylpropanol
3-(3',4'-dihydroxyphenyl)-1-propanol
Conditions | Yield |
---|---|
With zeolite beta (Zeolyst, CP814C) In water at 250℃; under 37503.8 Torr; for 6h; Reagent/catalyst; Sealed tube; Inert atmosphere; | 98% |
8-methylnonanoic acid
3-Guaiacylpropanol
8-methylnonanoic acid 3-(4-hydroxy-3-methoxyphenyl)propyl ester
Conditions | Yield |
---|---|
novozyme 435 at 50℃; for 16h; Enzymatic reaction; Neat (no solvent); | 95.4% |
3-Guaiacylpropanol
allyl bromide
3-(4-(allyloxy)-3-methoxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With potassium carbonate In acetone | 83% |
With potassium carbonate; potassium iodide In acetone Reflux; | 46% |
With ethanol; potassium carbonate |
3-Guaiacylpropanol
ethyl acetate
3-(4-hydroxy-3-methoxyphenyl)-propyl acetate
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate; silica gel at 20℃; for 9h; | 80% |
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With 1,1,3-trimethyl-3-phenylindan-4',5-dicarboxylic acid In dichloromethane | 74% |
3-Guaiacylpropanol
Conditions | Yield |
---|---|
With 2-Picolinic acid; potassium phosphate; copper(l) iodide In dimethyl sulfoxide at 100℃; for 20h; Glovebox; Sealed tube; | 74% |
3-Guaiacylpropanol
tert-butyldimethylsilyl chloride
Conditions | Yield |
---|---|
With dmap; triethylamine In dichloromethane for 24h; silylation; 0 deg C up to RT; | 55% |
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; for 48h; Mitsunobu Displacement; chemoselective reaction; | 50% |
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; for 48h; Mitsunobu Displacement; chemoselective reaction; | 50% |
3-Guaiacylpropanol
4-nitrobenzaldehdye
8-hydroxy-7-methoxy-1-(4-nitrophenyl)-1,3,4,5-tetrahydrobenzo[c]oxepine
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate; aluminium trichloride In 1,4-dioxane at 20℃; for 168h; oxa-Pictet-Spengler reaction; | 47% |
3-Guaiacylpropanol
3-(3'-methoxy-4'-hydroxyphenyl)propionaldehyde
Conditions | Yield |
---|---|
With dimethyl sulfoxide; triethylamine In dichloromethane at 20℃; for 0.5h; | 27.5% |
With coniferyl alcohol dehydrogenase isosyme I from cell free extract of Stretomyces sp. NL15-2K; nicotinamide adenine dinucleotide pH=9.5; Kinetics; Concentration; pH-value; Reagent/catalyst; Glycine-NaOH buffer; Enzymatic reaction; |
pyridine
3-Guaiacylpropanol
4-nitro-benzoyl chloride
2-methoxy-1-(4-nitro-benzoyloxy)-4-[3-(4-nitro-benzoyloxy)-propyl]-benzene
Conditions | Yield |
---|---|
With potassium hydroxide; ethanol; chloroform | |
Multi-step reaction with 4 steps 1: K2CO3; ethanol 2: 240 °C 3: KOH; water / 170 - 175 °C 4: ozone; ethyl acetate / und Erwaermen des Reaktionsprodukts mit Wasser View Scheme |
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