As 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
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inquiryProduct Name: 2,2,2-TRIFLUORO-1-(4-HYDROXY-PHENYL)-ETHANONE Synonyms: 2,2,2-TRIFLUORO-1-(4-HYDROXY-PHENYL)-ETHANONE;Ethanone, 2,2,2-trifluoro-1-(4-hydroxyphenyl)-;3-(1-amino-2,2,2-trifluoroethyl)phenol;4'-Hydroxy-2,2,2-trifluoroace
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inquiry1.In No Less 10 years exporting experience. you 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 Specializ
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inquiry2,2,2-TRIFLUORO-1-(4-HYDROXY-PHENYL)-ETHANONE CAS:1823-63-8 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 h
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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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inquiryA substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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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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inquirySuperior quality moderate price & quick delivery Appearance:powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used to make other chemic
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inquiry2,2,2-TRIFLUORO-1-(4-HYDROXY-PHENYL)-ETHANONE Chemical Properties Melting point 114 °C Boiling point 261.9±35.0 °C(Predicted) density 1.400±0.06 g/cm3(Predicted) storage temp. Sealed in dry,2-8°C pka 7.60&
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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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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
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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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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
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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
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
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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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inquiry2,2,2-Trifluoro-1-(4-hydroxy-phenyl)-ethanone cas 1823-63-8Appearance: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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inquiryreagent grade ex stockAppearance:white or off-white crystalline powder Storage:Keep away of light,cool place Package:1L 5L 10L 25L bottle Application:pharma intermediate Transportation:by Fedex, ship or plane
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inquiryBest quality with low price Storage:ln stock Package:25kg/Barrel Application:Chemicals Transportation:Express/Sea/Air Port:Shanghai
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inquiry1823-63-8 Application:intermediate
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inquiryR & D enterprises have their own stock in stockAppearance:To be subject to the object Package:Customized Application:pharmaceutical intermediates Transportation:Air Port:Shanghai;Guangzhou
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inquiryGood Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen
high purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
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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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inquiryBest Seller, High Quality, Competitive Price, Fast Delivery, Quick ResponseAppearance:powder, or liquid Storage:Stored in room temperature, ventilated place Package:Bottle, barrel, cargo, container, etc. Application:Pharmaceuticals, intermediates, AP
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inquiryOur mission is to provide high-quality and innovative products to our customers. By offering a broad range of products, custom synthesis and personalized services, Bide can help scientists speeding up their research in the chemical and pharmaceutical
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inquiry4'-methoxy-2,2,2-trifluoroacetophenone
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
Conditions | Yield |
---|---|
With boron tribromide In dichloromethane at -78 - 20℃; for 16h; | 96% |
With lithium chloride In N,N-dimethyl-formamide for 2h; Heating; | 88% |
With boron tribromide In dichloromethane at -78 - 20℃; | 88% |
1-[4-[{(1,1-dimethylethyl)dimethylsilyl}oxy]phenyl]-2,2,2-trifluoroethan-1-one
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
Conditions | Yield |
---|---|
With tetrabutyl ammonium fluoride In tetrahydrofuran at 20℃; | 90% |
(4-bromophenoxy)trimethylsilane
ethyl trifluoroacetate,
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
Conditions | Yield |
---|---|
With n-butyllithium In tetrahydrofuran | 68% |
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 100 percent / imidazole / dimethylformamide / 0 - 20 °C 2: 56 percent / Mg / tetrahydrofuran / 20 °C 3: 90 percent / TBAF / tetrahydrofuran / 20 °C View Scheme |
t-butyldimethylsilyl-4-bromophenol
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 56 percent / Mg / tetrahydrofuran / 20 °C 2: 90 percent / TBAF / tetrahydrofuran / 20 °C View Scheme |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethyl alcohol
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
Conditions | Yield |
---|---|
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In ethyl acetate for 12h; Reflux; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1.1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 20 °C 1.2: 4 h / Acidic conditions 2.1: 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione / ethyl acetate / 12 h / Reflux View Scheme |
bromoacetic acid tert-butyl ester
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
C14H15F3O4
Conditions | Yield |
---|---|
With potassium carbonate; potassium iodide In acetonitrile at 120℃; for 0.666667h; Microwave irradiation; | 95% |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
Conditions | Yield |
---|---|
With tetra-(n-butyl)ammonium iodide; caesium carbonate In N,N-dimethyl-formamide at 65℃; | 90% |
4-chloromethyl-3,5-dimethylisoxazole
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 16h; | 90% |
(S)-Methyl lactate
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
Conditions | Yield |
---|---|
Stage #1: (S)-Methyl lactate; 2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one With triphenylphosphine In dichloromethane at 0℃; for 0.166667h; Mitsunobu Displacement; Stage #2: With diethylazodicarboxylate In dichloromethane at 0 - 20℃; for 8h; Mitsunobu Displacement; | 78% |
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate In ethyl acetate Reflux; | 76.8% |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
(2S,3R)-1,3-di-O-benzoyl-2-(tert-butoxycarbonylamino)-(4E)-tetradecene-1,3,14-triol
(2S,3R)-1,3-di-O-benzoyl-2-(tert-butoxycarbonylamino)-14-O-(4'-(trifluoroacetyl)phenyl)-(4E)-tetradecene-1,3,14-triol
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In dichloromethane at 0 - 20℃; Mitsunobu reaction; | 74% |
(R)-Methyl lactate
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
Conditions | Yield |
---|---|
Stage #1: (R)-Methyl lactate; 2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one With triphenylphosphine In dichloromethane at 0℃; for 0.166667h; Mitsunobu Displacement; Stage #2: With diethylazodicarboxylate In dichloromethane at 0 - 20℃; for 8h; Mitsunobu Displacement; | 74% |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
2-(tert-butyldimethylsilyloxy)ethyl bromide
1-(4-(2-((tert-butyldimethylsilyl)oxy)ethoxy)phenyl)-2,2,2-trifluoroethan-1-one
Conditions | Yield |
---|---|
With 18-crown-6 ether; potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 60℃; for 12h; Inert atmosphere; Schlenk technique; | 70% |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
ethyl bromoacetate
C12H11F3O4
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 0 - 60℃; for 4h; Inert atmosphere; | 33% |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
2-(diethylamino)ethyl chloride
2,2,2-Trifluor-4'-(2-diethylamino-ethoxy)-acetophenon
Conditions | Yield |
---|---|
(i) Na, (ii) /BRN= 605300/; Multistep reaction; |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
4-pentylbenzoic acid
4-Pentyl-benzoic acid 4-(2,2,2-trifluoro-acetyl)-phenyl ester
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
4-trans-pentyl-cyclohexane-1-carboxylic acid
4-Pentyl-cyclohexanecarboxylic acid 4-(2,2,2-trifluoro-acetyl)-phenyl ester
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
trans-trans-4-n-pentylcyclohexyl-cyclohexane-4'-carboxylic acid
4'-Pentyl-bicyclohexyl-4-carboxylic acid 4-(2,2,2-trifluoro-acetyl)-phenyl ester
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
p-(4-trans-n-Pentylcyclohexyl)benzoic acid
4-(4-Pentyl-cyclohexyl)-benzoic acid 4-(2,2,2-trifluoro-acetyl)-phenyl ester
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethyl alcohol
Conditions | Yield |
---|---|
With sodium tetrahydroborate In 1,4-dioxane; isopropyl alcohol at 20℃; Rate constant; | |
With sodium cyanoborohydride; zinc(II) iodide In 1,1-dichloroethane at 20℃; for 18h; |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
(2S,3R)-2-amino-14-O-[4'-[3-(trifluoromethyl)diazirin-3-yl]phenyl]-(4E)-tetradecene-1,3,14-triol
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1: 74 percent / DIAD; Ph3P / CH2Cl2 / 0 - 20 °C 2: 99 percent / hydroxylamine hydrochloride; pyridine / ethanol / 12 h / 50 - 60 °C 3: 99 percent / triethylamine; DMAP / CH2Cl2 / 0 - 20 °C 4: 80 percent / ammonia / CH2Cl2 / -78 - 20 °C 5: 97 percent / NaOH; MeOH / 20 °C 6: 82 percent / I2; Et3N / methanol / 1 h / 20 °C 7: 80 percent / aq. HCl / tetrahydrofuran / 20 °C View Scheme |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
(2S,3R)-2-(tert-butoxycarbonylamino)-14-O-[4'-[3-(trifluoromethyl)diazirin-3-yl]phenyl]-(4E)-tetradecene-1,3,14-triol
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1: 74 percent / DIAD; Ph3P / CH2Cl2 / 0 - 20 °C 2: 99 percent / hydroxylamine hydrochloride; pyridine / ethanol / 12 h / 50 - 60 °C 3: 99 percent / triethylamine; DMAP / CH2Cl2 / 0 - 20 °C 4: 80 percent / ammonia / CH2Cl2 / -78 - 20 °C 5: 97 percent / NaOH; MeOH / 20 °C 6: 82 percent / I2; Et3N / methanol / 1 h / 20 °C View Scheme |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
(2S,3R)-2-(tert-butoxycarbonylamino)-14-O-[4'-[3-(trifluoromethyl)diaziridin-3-yl]phenyl]-(4E)-tetradecene-1,3,14-triol
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: 74 percent / DIAD; Ph3P / CH2Cl2 / 0 - 20 °C 2: 99 percent / hydroxylamine hydrochloride; pyridine / ethanol / 12 h / 50 - 60 °C 3: 99 percent / triethylamine; DMAP / CH2Cl2 / 0 - 20 °C 4: 80 percent / ammonia / CH2Cl2 / -78 - 20 °C 5: 97 percent / NaOH; MeOH / 20 °C View Scheme |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
(2S,3R)-1,3-di-O-benzoyl-2-(tert-butoxycarbonylamino)-14-O-[4'-[3-(trifluoromethyl)diaziridin-3-yl]phenyl]-(4E)-tetradecene-1,3,14-triol
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 74 percent / DIAD; Ph3P / CH2Cl2 / 0 - 20 °C 2: 99 percent / hydroxylamine hydrochloride; pyridine / ethanol / 12 h / 50 - 60 °C 3: 99 percent / triethylamine; DMAP / CH2Cl2 / 0 - 20 °C 4: 80 percent / ammonia / CH2Cl2 / -78 - 20 °C View Scheme |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
(2S,3R)-1,3-di-O-benzoyl-2-(tert-butoxycarbonylamino)-14-O-(4'-(trifluoroacetyl)phenyl)-(4E)-tetradecene-1,3,14-triol oxime
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 74 percent / DIAD; Ph3P / CH2Cl2 / 0 - 20 °C 2: 99 percent / hydroxylamine hydrochloride; pyridine / ethanol / 12 h / 50 - 60 °C View Scheme |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
(2S,3R)-1,3-di-O-benzoyl-2-(tert-butoxycarbonylamino)-14-O-(4'-(trifluoroacetyl)phenyl)-(4E)-tetradecene-1,3,14-triol O-tosyl oxime
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: 74 percent / DIAD; Ph3P / CH2Cl2 / 0 - 20 °C 2: 99 percent / hydroxylamine hydrochloride; pyridine / ethanol / 12 h / 50 - 60 °C 3: 99 percent / triethylamine; DMAP / CH2Cl2 / 0 - 20 °C View Scheme |
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
1-(4-Chlor-phenyl)-2-<4-(2-diethylamino-ethoxy)-phenyl>-3,3,3-trifluor-propan-2-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: (i) Na, (ii) /BRN= 605300/ View Scheme |
dibromodifluoromethane
2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one
4'-bromodifluoromethoxy-2,2,2-trifluoroacetophenone
Conditions | Yield |
---|---|
Stage #1: 2,2,2-trifluoro-1-(4-hydroxyphenyl)ethan-1-one With sodium hydride In 1,3-dimethyl-2-imidazolidinone at 20℃; for 0.5h; Stage #2: dibromodifluoromethane In 1,3-dimethyl-2-imidazolidinone at 0 - 10℃; Stage #3: With potassium tert-butylate In 1,3-dimethyl-2-imidazolidinone at 20℃; for 1h; |
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