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inquiryGood quality Good price Promptly delivery Appearance:White or off-white Solid Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:intermediate Transportation:Ac
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inquiryDayangChem 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
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inquiryOur Advantage Rich Experience Our products are sold all over Europe,North&South America, Sino-East, Asia and pacific area as well as Africa,we establish long term. Quality service Company cooperates with research institutes. We strictly con
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inquiryAppearance:White to off-white powder Storage:room temperature Package:25kg/drum Application:Chemicals Transportation:Express/Sea/Air Port:any port in china
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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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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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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
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 present
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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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inquiryOur company was built in 2009 with an ISO certificate.In the past 6 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
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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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inquiryZhenyu biotech exported this product to many countries and regions at best price. if you are looking for the material's manufacturer or supplier in china, zhenyu biotech is your best choice. pls contact with us freely for getting detailed
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inquiry1.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
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inquiryhigh 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
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Shanghai Lonwin Chemical company is a subsidiary of Lonwin Industry Group Limited, was established in 2011 and is headquartered in Shanghai, adjacent to China National Convention and Exhibition Center and Hongqiao transportation hub.Lonwinchem is
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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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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
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inquiryOur clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
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inquiryAnsciep 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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inquiryWe product this chemical more than 10 years . We are very experience to export it to many countries, Our superior & stable quality , competitive price gain warm reception from our customers. Application:Pharm intermediate
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inquiryBenzenepropanol,4-hydroxy- cas 10210-17-0Appearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
3-(4-hydroxyphenyl)propionic acid methyl ester
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
Stage #1: 3-(4-hydroxyphenyl)propionic acid methyl ester With lithium aluminium tetrahydride In tetrahydrofuran at 20℃; for 4 - 5h; Heating / reflux; Stage #2: With sodium hydroxide; water In tetrahydrofuran; ethyl acetate | 100% |
Stage #1: 3-(4-hydroxyphenyl)propionic acid methyl ester With lithium aluminium tetrahydride In tetrahydrofuran at 20℃; for 4 - 5h; Heating / reflux; Stage #2: With sodium hydroxide In tetrahydrofuran; water; ethyl acetate at 20℃; Stage #3: With hydrogenchloride In tetrahydrofuran; water; ethyl acetate pH=7.0; | 100% |
With lithium aluminium tetrahydride In tetrahydrofuran at 20℃; for 4 - 5h; Heating / reflux; | 100% |
4-hydroxyphenylpropionic acid
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With borane-THF; Trimethyl borate In tetrahydrofuran at 0℃; for 4h; Inert atmosphere; | 99% |
With sodium tetrahydroborate; Trimethyl borate; dimethyl sulfate In tetrahydrofuran at 20℃; for 1.5h; | 98% |
With dimethylsulfide borane complex In tetrahydrofuran at 0 - 20℃; | 98% |
para-coumaryl alcohol
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With palladium 10% on activated carbon; hydrogen In methanol at 20℃; for 12h; | 98% |
methyl 3-(4-acetyloxyphenyl)propanoate
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With lithium borohydride In tetrahydrofuran at 70℃; for 22h; | 95.5% |
With lithium aluminium tetrahydride; diethyl ether |
3-(4-hydroxy-phenyl)-propionic acid ethyl ester
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran at 0 - 20℃; for 1h; Inert atmosphere; | 95% |
Stage #1: 3-(4-hydroxy-phenyl)-propionic acid ethyl ester With lithium aluminium tetrahydride In tetrahydrofuran for 6h; Heating / reflux; Stage #2: With ethyl acetate; sodium sulfate In tetrahydrofuran; water Stage #3: With hydrogenchloride In tetrahydrofuran; water pH=7.0; | 68% |
With lithium aluminium tetrahydride In tetrahydrofuran at 55℃; for 12h; | 13.5 g |
Multi-step reaction with 3 steps 1: 89.1 percent / K2CO3; NaI / acetone / 48 h / Heating 2: 66.2 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating 3: 84.3 percent / H2 / 10 percent Pd/C / ethanol / 20 °C / 760 Torr View Scheme |
3-(4-acetoxyphenyl)propyl acetate
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With aluminum oxide In neat (no solvent) at 65℃; for 0.0416667h; microwave irradiation; | 92% |
3-[4-(benzyloxy)phenyl]propan-1-ol
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With hydrogen; palladium on activated charcoal In acetic acid | 89% |
With hydrogen; palladium on activated charcoal In ethanol at 20℃; under 760 Torr; Hydrogenolysis; | 84.3% |
With hydrogen; palladium on activated charcoal In ethanol Ambient temperature; | 0.149 g |
p-Coumaric Acid
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With whole cell cultures of dichomitus albidofuscus at 24℃; for 72h; Darkness; Microbiological reaction; | 82% |
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 4 steps 1.1: pyridine / 1 h / 20 °C 2.1: chloroformic acid ethyl ester; triethylamine / 1,4-dioxane / 1 h / Inert atmosphere 2.2: 1 h / Inert atmosphere 3.1: potassium hydroxide / ethanol / 8 h / Inert atmosphere 4.1: 5%-palladium/activated carbon; hydrogen / ethyl acetate / 6 h / 20 °C / 2250.23 Torr View Scheme |
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
aluminum oxide for 0.183333h; Irradiation; | 78% |
With cerium(IV) triflate In acetonitrile at 20℃; for 0.25h; | 75% |
4-(3-hydroxypropyl)-2,6-di-tert-butylphenol
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
at 324℃; for 11h; | 76% |
4-(3-hydroxypropyl)-2,6-di-tert-butylphenol
A
3-(4-hydroxyphenyl)propan-1-ol
B
2-tert-butyl-4-(3-hydroxypropyl)phenol
Conditions | Yield |
---|---|
at 280 - 300℃; for 24h; Inert atmosphere; | A 57% B 9% |
4-hydroxyphenylpropionic acid
A
3-(4-hydroxyphenyl)propan-1-ol
B
4-(3-hydroxypropyl)cyclohex-3-enol
Conditions | Yield |
---|---|
With samarium diiodide; water; triethylamine In tetrahydrofuran at 20℃; for 3h; Inert atmosphere; | A 48% B 23% |
(E)-4-(3-hydroxyprop-1-enyl)phenol
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With 5%-palladium/activated carbon; hydrogen In ethyl acetate at 20℃; under 2250.23 Torr; for 6h; | 48% |
3-(4-Hydroxy-phenyl)-1-(2,4,6-trihydroxy-phenyl)-propan-1-on
A
3-(4-hydroxyphenyl)propan-1-ol
B
4-hydroxyphenylpropionic acid
C
recorcinol
Conditions | Yield |
---|---|
With sodium hydroxide; sodium tetrahydroborate In water at 100℃; Product distribution; | A 22% B 8% C 38% |
acetic acid 4-[3-oxo-3-(2,4,6-triacetoxy-phenyl)propyl]phenyl ester
A
3,5-dihydroxyphenol
B
3-(4-hydroxyphenyl)propan-1-ol
C
2-(3-(4-hydroxyphenyl)propyl)benzene-1,3,5-triol
Conditions | Yield |
---|---|
With sodium tetrahydroborate In ethanol Product distribution; | A 7.5% B 6% C 6% |
3-(p-methoxyphenyl)-1-propanol
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With hydrogen bromide; acetic acid |
3-(4-hydroxyphenyl)propanoic acid amide
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With ethanol; sodium |
4-(3-chloropropyl)phenol
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With sodium acetate; acetic acid Erwaermen des Reaktionsprodukts mit Alkalilauge; |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether | A 2 mg B 5 mg |
dehydrocuspidiol
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With zinc In acetic acid for 1h; Heating; | 0.004 g |
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With lithium borohydride In tetrahydrofuran for 16h; Yield given; |
3-(4'-acetoxyphenyl)propionic acid
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 100 percent / K2CO3 / dimethylformamide / 23 h / 20 °C 2: 95.5 percent / LiBH4 / tetrahydrofuran / 22 h / 70 °C View Scheme |
ethyl 3-(4-(benzyloxy)phenyl)propanoate
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 66.2 percent / LiAlH4 / tetrahydrofuran / 2 h / Heating 2: 84.3 percent / H2 / 10 percent Pd/C / ethanol / 20 °C / 760 Torr View Scheme |
4-hydroxyphenylpropionic acid
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: tetrahydrofuran / 6 h / Ambient temperature 2: LiBH4 / tetrahydrofuran / 16 h View Scheme |
4-benzyloxybenzyl alcohol
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1: 2.840 g / thionyl chloride / benzene; pyridine / 1 h / Ambient temperature 2: 0.603 g / NaH / paraffin; dimethylformamide / 3 h / Ambient temperature 3: 0.370 g / KON / ethanol; H2O / 3 h / Heating 4: 0.249 g / 150 - 160 °C / 15 - 20 Torr 5: 1.663 g / diethyl ether / 2 h / Ambient temperature 6: 1.305 g / LiAlH4 / diethyl ether; tetrahydrofuran / 1.) room temperature, 1 h, 2.) reflux, 1 h 7: 0.149 g / H2 / 10percent Pd-charcoal / ethanol / Ambient temperature View Scheme | |
Multi-step reaction with 7 steps 1: 2.840 g / thionyl chloride / benzene; pyridine / 1 h / Ambient temperature 2: diethyl malonate / paraffin; dimethylformamide / 3 h / Ambient temperature 3: 0.370 g / KON / ethanol; H2O / 3 h / Heating 4: 0.249 g / 150 - 160 °C / 15 - 20 Torr 5: 1.663 g / diethyl ether / 2 h / Ambient temperature 6: 1.305 g / LiAlH4 / diethyl ether; tetrahydrofuran / 1.) room temperature, 1 h, 2.) reflux, 1 h 7: 0.149 g / H2 / 10percent Pd-charcoal / ethanol / Ambient temperature View Scheme |
4-[4-(3-hydroxy-propyl)-phenoxy]-2-methyl-but-2-en-1-ol
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 0.088 g / manganese dioxide / CHCl3 / 4 h / Ambient temperature 2: 0.004 g / Zn / acetic acid / 1 h / Heating View Scheme |
methyl (E)--2-methylcrotonate
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 0.077 g / LiAlH4 / tetrahydrofuran; diethyl ether / 1.) room temperature, 1h, 2.) reflux, 2 h 2: 0.088 g / manganese dioxide / CHCl3 / 4 h / Ambient temperature 3: 0.004 g / Zn / acetic acid / 1 h / Heating View Scheme |
methyl 3-(4-benzyloxyphenyl)propanoate
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.305 g / LiAlH4 / diethyl ether; tetrahydrofuran / 1.) room temperature, 1 h, 2.) reflux, 1 h 2: 0.149 g / H2 / 10percent Pd-charcoal / ethanol / Ambient temperature View Scheme |
3-(4-benzyloxyphenyl)propanoic acid
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 1.663 g / diethyl ether / 2 h / Ambient temperature 2: 1.305 g / LiAlH4 / diethyl ether; tetrahydrofuran / 1.) room temperature, 1 h, 2.) reflux, 1 h 3: 0.149 g / H2 / 10percent Pd-charcoal / ethanol / Ambient temperature View Scheme | |
Multi-step reaction with 2 steps 1: 85 percent / lithium aluminium hydride / diethyl ether / 2.5 h / Heating 2: 89 percent / hydrogen / 10percent palladium-carbon / acetic acid View Scheme |
ortho-nitrophenyl selenocyanate
3-(4-hydroxyphenyl)propan-1-ol
4-[3-(2-Nitro-phenylselanyl)-propyl]-phenol
Conditions | Yield |
---|---|
With tributylphosphine In tetrahydrofuran for 5h; Ambient temperature; | 100% |
2-(3-bromopropyl)isoindole-1,3-dione
3-(4-hydroxyphenyl)propan-1-ol
2-{3-[4-(3-hydroxy-propyl)-phenoxy]-propyl}-isoindole-1,3-dione
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 24h; Heating; | 100% |
With potassium carbonate In acetone for 24h; Heating; | 73% |
3-(4-hydroxyphenyl)propan-1-ol
carbonic acid dimethyl ester
3-(4-hydroxyphenyl)propyl methyl carbonate
Conditions | Yield |
---|---|
With 1,8-diazabicyclo[5.4.0]undec-7-ene Reflux; | 100% |
With zeolite NaY at 90℃; for 240h; Reagent/catalyst; |
2-(2,6-dimethyl-4-tritylphenoxy)ethyl toluene-4-sulfonate
3-(4-hydroxyphenyl)propan-1-ol
3-{4-[2-(2,6-dimethyl-4-tritylphenoxy)ethoxy]phenyl}propan-1-ol
Conditions | Yield |
---|---|
With sodium ethanolate In acetonitrile for 6h; Heating; | 99% |
3-(4-hydroxyphenyl)propan-1-ol
2,6-dibromo-4-(3-hydroxypropyl)phenol
Conditions | Yield |
---|---|
With bromine In acetic acid at 20℃; | 99% |
With bromine; acetic acid at 20℃; |
3-(4-hydroxyphenyl)propan-1-ol
methanesulfonyl chloride
dimesylate of p-hydroxydihydrocinnamyl alcohol
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere; | 98% |
With triethylamine In dichloromethane at 0 - 20℃; for 16h; | 61% |
With triethylamine In dichloromethane at 0 - 20℃; for 16h; | 61% |
3-(4-hydroxyphenyl)propan-1-ol
chloroformic acid ethyl ester
Conditions | Yield |
---|---|
With triethylamine In acetonitrile at -80 - 20℃; Inert atmosphere; | 98% |
3-(4-hydroxyphenyl)propan-1-ol
dibenzyl [[bis(benzyloxy)phosphoryl]oxy]phosphonate
Conditions | Yield |
---|---|
With tetrahexylammonium iodide; silver(l) oxide In dichloromethane at 20℃; for 20h; | 97% |
3-(4-hydroxyphenyl)propan-1-ol
4-(3-bromopropyl)phenol
Conditions | Yield |
---|---|
With hydrogen bromide at 80℃; for 20h; | 96% |
With carbon tetrabromide; triphenylphosphine In dichloromethane Appel reaction; Cooling with ice; | 95% |
With hydrogen bromide In water at 80℃; for 20h; | 92% |
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide at 20℃; for 40h; | 96% |
3-iodopyridine
3-(4-hydroxyphenyl)propan-1-ol
Conditions | Yield |
---|---|
With 2-Picolinic acid; potassium phosphate; copper(l) iodide In dimethyl sulfoxide at 80℃; for 21h; Inert atmosphere; chemoselective reaction; | 96% |
Conditions | Yield |
---|---|
With rubidium fluoride In acetonitrile at 80℃; for 0.5h; | 96% |
3-(4-hydroxyphenyl)propan-1-ol
benzyl chloride
3-[4-(benzyloxy)phenyl]propan-1-ol
Conditions | Yield |
---|---|
With potassium carbonate In ethanol for 6h; Inert atmosphere; Reflux; | 95% |
With potassium carbonate In ethanol for 3h; Heating; | 94% |
With sodium hydride 1.) DMF, 50 deg C 2.) 50 deg C; Yield given. Multistep reaction; |
3-(4-hydroxyphenyl)propan-1-ol
benzyl bromide
3-[4-(benzyloxy)phenyl]propan-1-ol
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 20℃; for 12h; | 95% |
With potassium carbonate In N,N-dimethyl-formamide at 20℃; | 92% |
With sodium hydride In N,N-dimethyl-formamide for 12h; Heating; | 90% |
3-(4-hydroxyphenyl)propan-1-ol
(2-methylallyl)tertiobutyl-dimethylsilane
3-(4-((tert-butyl(dimethyl)silyl)oxy)phenyl)propan-1-ol
Conditions | Yield |
---|---|
Stage #1: 3-(4-hydroxyphenyl)propan-1-ol; (2-methylallyl)tertiobutyl-dimethylsilane With scandium tris(trifluoromethanesulfonate) In various solvent(s) at 20℃; for 4h; Stage #2: With water In various solvent(s) at 20℃; for 3h; | 95% |
di-tert-butyl dicarbonate
3-(4-hydroxyphenyl)propan-1-ol
3-(4-t-butoxycarbonyl)phenyl-1-propanol
Conditions | Yield |
---|---|
With 18-crown-6 ether; potassium carbonate In dichloromethane at 0 - 20℃; Inert atmosphere; | 95% |
With 18-crown-6 ether; potassium carbonate In dichloromethane at 0 - 20℃; Inert atmosphere; | 95% |
3-(4-hydroxyphenyl)propan-1-ol
methyl iodide
3-(p-methoxyphenyl)-1-propanol
Conditions | Yield |
---|---|
With potassium carbonate In acetone | 94.9% |
With potassium carbonate In diethyl ether; acetone | 94.93% |
vinyl laurate
3-(4-hydroxyphenyl)propan-1-ol
3-(4-hydroxyphenyl)propyl dodecanoate
Conditions | Yield |
---|---|
With lipase B from Candida sp. expressed in Aspergillus niger In aq. buffer for 20h; pH=7.2; Green chemistry; Enzymatic reaction; | 94.1% |
With Candida antarctica lipase B in agarose gel droplets Pickering-stabilized by UiO-66/Fe3O4 nanoparticles In acetone at 20℃; for 12h; Reagent/catalyst; Enzymatic reaction; |
3-(4-hydroxyphenyl)propan-1-ol
A
4,6-dichloro-2-hydroxy-1,3,5-triazine
Conditions | Yield |
---|---|
In dichloromethane at 25℃; for 0.25h; | A n/a B 94% |
3-(4-hydroxyphenyl)propan-1-ol
4-(3-iodopropyl)phenol
Conditions | Yield |
---|---|
With hydrogen iodide at 100℃; | 94% |
With 1H-imidazole; iodine; triphenylphosphine In dichloromethane at 20℃; for 5h; | 32% |
With hydrogen iodide |
3-(4-hydroxyphenyl)propan-1-ol
tert-butylchlorodiphenylsilane
3-(4-hydroxyphenyl)-1-(tert-butyldiphenylsilyloxy)propane
Conditions | Yield |
---|---|
With 1H-imidazole; dmap In N,N-dimethyl-formamide at 0 - 20℃; Inert atmosphere; | 94% |
3-(4-hydroxyphenyl)propan-1-ol
2,2,2-trichloroacetophenone
Conditions | Yield |
---|---|
With N,N,N',N'',N'''-pentamethyldiethylenetriamine In acetonitrile at 20 - 25℃; for 12h; | 94% |
3-(4-hydroxyphenyl)propan-1-ol
4-Phenylbutyric acid
Conditions | Yield |
---|---|
tetrachlorobis(tetrahydrofuran)hafnium(IV) In toluene for 6h; Heating; | A n/a B 93% C n/a |
3-(4-hydroxyphenyl)propan-1-ol
prenyl bromide
3-methyl-2-butenyl 3-[4-(3-methyl-2-butenyloxy)-phenyl]propyl ether
Conditions | Yield |
---|---|
With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; for 2h; | 93% |
3-(4-hydroxyphenyl)propan-1-ol
4-Phenylbutyric acid
Conditions | Yield |
---|---|
tetrachlorobis(tetrahydrofuran)hafnium(IV) In toluene for 6h; Heating; | 93% |
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