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Cas:37470-42-1
Min.Order:1 Kilogram
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Cas:37470-42-1
Min.Order:1 Gram
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Cas:37470-42-1
Min.Order:1 Kilogram
FOB Price: $2.0
Type:Lab/Research institutions
inquiryShandong Mopai Biotechnology 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 chemicals. W
Cas:37470-42-1
Min.Order:1 Gram
Negotiable
Type:Lab/Research institutions
inquiryhigh qualityAppearance:white crystalline powder Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
hight degree of purity Application:Fine chemical intermediates, used as the main raw material for he synthesis of various pesticides, medicines, surfactants, polymer monomers, Ond Ontifungal agents
Cas:37470-42-1
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquiry4'-ETHOXY-2'-HYDROXYACETOPHENONEAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
factory?direct?sale Application:Fine chemical intermediates, used as the main raw material for the synthesis of various pesticides, medicines, surfactants, polymer monomers, and antifungal agents
factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin
FINETECH INDUSTRY LIMITED is a LONDON based CRO company providing drug discovery & development services to worldwide clients. FINETECH INDUSTRY LIMITED supplies the 1-(4-Ethoxy-2-hydroxyphenyl)ethanone, CAS:37470-42-1 with the most competitive price
Cas:37470-42-1
Min.Order:0
Negotiable
Type:Trading Company
inquiry2',4'-dihydroxy-4-acetophenone
ethyl iodide
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With potassium carbonate In acetone at 80℃; for 6h; | 97% |
With potassium carbonate In N,N-dimethyl-formamide for 4h; | 63% |
diethyl sulfate
2',4'-dihydroxy-4-acetophenone
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 2h; Reflux; | 78% |
In acetone at 20℃; for 25h; Reflux; |
ethyl bromide
2',4'-dihydroxy-4-acetophenone
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 13h; Reflux; | 73.5% |
With potassium carbonate In acetone for 24h; Heating; Yield given; |
ethyl bromide
2',4'-dihydroxy-4-acetophenone
A
1-(4-ethoxy-2-hydroxyphenyl)ethanone
B
2',4'-dimethoxyacetophenone
Conditions | Yield |
---|---|
With potassium carbonate |
2',4'-dihydroxy-4-acetophenone
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With water; silver nitrate und Erwaermen des erhaltenen Silber-Salzes mit Aethyljodid in Aceton; |
7-ethoxy-2-methyl-chromen-4-one
sodium ethanolate
1-(4-ethoxy-2-hydroxyphenyl)ethanone
sodium ethanolate
A
1-(4-ethoxy-2-hydroxyphenyl)ethanone
B
propionic acid
7-ethoxy-2-phenyl-4H-chromen-4-one
sodium ethanolate
A
1-(4-ethoxy-2-hydroxyphenyl)ethanone
B
benzoic acid
sodium ethanolate
A
phenylacetic acid
B
1-(4-ethoxy-2-hydroxyphenyl)ethanone
sodium ethanolate
A
1-(4-ethoxy-2-hydroxyphenyl)ethanone
B
4-methoxybenzoic acid
sodium ethanolate
A
1-(4-ethoxy-2-hydroxyphenyl)ethanone
B
4-ethoxy-2-hydroxybenzoic acid
C
2-ethoxybenzoic acid
sodium ethanolate
A
1-(4-ethoxy-2-hydroxyphenyl)ethanone
B
3-ethoxybenzoic acid
2',4'-dihydroxy-4-acetophenone
ethyl iodide
A
2′,4′-diethoxyacetophenone
B
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With potassium carbonate |
2',4'-dihydroxy-4-acetophenone
ethyl iodide
A
1-(4-ethoxy-2-hydroxyphenyl)ethanone
B
2',4'-dimethoxyacetophenone
Conditions | Yield |
---|---|
With potassium carbonate |
7-ethoxy-2-phenyl-4H-chromen-4-one
A
O-ethyl resorcinol
B
1-(4-ethoxy-2-hydroxyphenyl)ethanone
C
benzoic acid
Conditions | Yield |
---|---|
Kalischmelze; |
recorcinol
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: zinc(II) chloride; hydrogenchloride / diethyl ether / 0.5 h / 0 °C 2: water / 2 h / Reflux 3: potassium carbonate / acetone / 2 h / Reflux View Scheme |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With hydrogen; palladium 10% on activated carbon In methanol for 24h; | 97% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
2-(2-acetylphenoxy)-1-bromoethane
1-(2-acetylphenoxy)-2-(2-acetyl-5-ethoxyphenoxy)ethane
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 80℃; | 88% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With pyrrolidine In ethanol at 80℃; for 10h; Kabe Chromanone Synthesis; | 85% |
morpholine
formaldehyd
1-(4-ethoxy-2-hydroxyphenyl)ethanone
A
1-[4-ethoxy-2-hydroxy-5-(morpholinomethyl)phenyl]ethanone
B
1-[4-ethoxy-2-hydroxy-3-(morpholinomethyl)phenyl]ethanone
Conditions | Yield |
---|---|
In ethanol; water at 120℃; Mannich reaction; | A 83% B 6% |
3-methyl-cyclopentanone
1-(4-ethoxy-2-hydroxyphenyl)ethanone
(1'S,3'R)-7-ethoxy-3'-methylspiro[chroman-2,1'-cyclopentan]-4-one
Conditions | Yield |
---|---|
Stage #1: 3-methyl-cyclopentanone; 1-(4-ethoxy-2-hydroxyphenyl)ethanone With cis-Hyp(tBu)-Thr(tBu)-TentaGel In methanol at 20℃; for 1h; Stage #2: In methanol at 110℃; for 0.183333h; Microwave irradiation; optical yield given as %ee; enantioselective reaction; | 83% |
5, 6-dimethyl-1,10-phenanthroline
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol at 50 - 55℃; for 0.2h; pH=7 - 8; | 82% |
1-(3,4,5-trimethoxyphenyl)-2-bromoethanone
1-(4-ethoxy-2-hydroxyphenyl)ethanone
(6-ethoxy-3-methylbenzofuran-2-yl)(3,4,5-trimethoxyphenyl)methanone
Conditions | Yield |
---|---|
With potassium carbonate In acetone for 18h; Reflux; | 81% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
N,N-Dimethylthiocarbamoyl chloride
O-2-acetyl-5-ethoxyphenyl N,N-dimethylcarbamothioate
Conditions | Yield |
---|---|
With 1,4-diaza-bicyclo[2.2.2]octane In N,N-dimethyl-formamide at 50℃; for 5h; Inert atmosphere; | 81% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
2-Methylcyclohexanone
C17H22O3
Conditions | Yield |
---|---|
Stage #1: 1-(4-ethoxy-2-hydroxyphenyl)ethanone; 2-Methylcyclohexanone With cis-Hyp(tBu)-Thr(tBu)-TentaGel In methanol at 20℃; for 1h; Stage #2: In methanol at 110℃; for 0.183333h; Microwave irradiation; optical yield given as %ee; enantioselective reaction; | 80% |
[2,2]bipyridinyl
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol at 50 - 55℃; for 0.2h; pH=7 - 8; | 79% |
3-methyl-cyclopentanone
1-(4-ethoxy-2-hydroxyphenyl)ethanone
C16H20O3
Conditions | Yield |
---|---|
Stage #1: 3-methyl-cyclopentanone; 1-(4-ethoxy-2-hydroxyphenyl)ethanone With trans-Hyp(tBu)-Thr(tBu)-TentaGel In methanol at 20℃; for 1h; Stage #2: In methanol at 110℃; for 0.183333h; Microwave irradiation; optical yield given as %ee; enantioselective reaction; | 78% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
benzaldehyde
7-ethoxy-2-phenyl-4H-chromen-4-one
Conditions | Yield |
---|---|
With pyrrolidine; iodine In dimethyl sulfoxide at 150℃; for 12h; | 78% |
N-ethyl-3-carbazolealdehyde
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With potassium hydroxide for 0.133333h; Claisen-Schmidt Condensation; Microwave irradiation; | 78% |
With potassium hydroxide Claisen-Schmidt Condensation; Sealed tube; Microwave irradiation; Green chemistry; | 78% |
Claisen-Schmidt Condensation; |
1,10-Phenanthroline
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol at 50 - 55℃; for 0.2h; pH=7 - 8; | 78% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
2-Methylcyclohexanone
(1'R,2'S)-7-ethoxy-2'-methylspiro[chroman-2,1'-cyclohexan]-4-one
Conditions | Yield |
---|---|
Stage #1: 1-(4-ethoxy-2-hydroxyphenyl)ethanone; 2-Methylcyclohexanone With trans-Hyp(tBu)-Thr(tBu)-TentaGel In methanol at 20℃; for 1h; Stage #2: In methanol at 110℃; for 0.183333h; Microwave irradiation; optical yield given as %ee; enantioselective reaction; | 76% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
bathophenanthroline
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol at 50 - 55℃; for 0.2h; pH=7 - 8; | 72% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
(carbethoxyethylidene)triphenylphosphorane
7-ethoxy-3,4-dimethyl-coumarin
Conditions | Yield |
---|---|
at 180℃; for 10h; | 66% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With sodium azide; iodine; sodium hydrogencarbonate In N,N-dimethyl-formamide at 100℃; for 2h; | 66% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
water
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol at 50 - 55℃; for 0.2h; pH=7 - 8; | 65% |
thiophene-2-carbaldehyde
1-(4-ethoxy-2-hydroxyphenyl)ethanone
7-ethoxy-3-hydroxy-2-(thiophen-2-yl)-4H-chromen-4-one
Conditions | Yield |
---|---|
Stage #1: thiophene-2-carbaldehyde; 1-(4-ethoxy-2-hydroxyphenyl)ethanone With methanol; sodium hydroxide for 3h; Reflux; Stage #2: With dihydrogen peroxide at 20℃; | 55% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With sodium azide; iodine; sodium hydrogencarbonate In water at 100℃; for 2h; | 54% |
benzothiophene-3-carboxaldehyde
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol; water at 20℃; Claisen-Schmidt Condensation; | 52% |
morpholine
1-(4-ethoxy-2-hydroxyphenyl)ethanone
Conditions | Yield |
---|---|
With sulfur at 130℃; for 16h; | 52% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
benzaldehyde
Conditions | Yield |
---|---|
Stage #1: 1-(4-ethoxy-2-hydroxyphenyl)ethanone; benzaldehyde With methanol; sodium hydroxide for 3h; Reflux; Stage #2: With dihydrogen peroxide at 20℃; | 50% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
4-formylphenylboronic acid,
7-ethoxy-3-hydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one
Conditions | Yield |
---|---|
Stage #1: 1-(4-ethoxy-2-hydroxyphenyl)ethanone; 4-formylphenylboronic acid, With methanol; sodium hydroxide for 3h; Reflux; Stage #2: With dihydrogen peroxide at 20℃; | 40% |
1-(4-ethoxy-2-hydroxyphenyl)ethanone
benzaldehyde
4'-ethoxy-2'-hydroxy-trans-chalcone
Conditions | Yield |
---|---|
With potassium hydroxide In methanol; water at 20℃; for 24h; Aldol Condensation; | 20% |
carbon disulfide
1-(4-ethoxy-2-hydroxyphenyl)ethanone
7-Ethoxy-4-hydroxy-2H-1-benzopyran-2-thione
Conditions | Yield |
---|---|
With potassium tert-butylate In benzene Ambient temperature; | 18% |
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