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37470-42-1

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37470-42-1 Usage

Preparation

Preparation by reaction of ethyl iodide on resacetophenone, ? with potassium hydroxide in refluxing ethanol (25%) or boiling acetone ; ? with potassium carbonate in boiling acetone.

Check Digit Verification of cas no

The CAS Registry Mumber 37470-42-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,4,7 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 37470-42:
(7*3)+(6*7)+(5*4)+(4*7)+(3*0)+(2*4)+(1*2)=121
121 % 10 = 1
So 37470-42-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O3/c1-3-13-8-4-5-9(7(2)11)10(12)6-8/h4-6,12H,3H2,1-2H3

37470-42-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-ethoxy-2-hydroxyphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 4'-Ethoxy-2'-hydroxyacetophenone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:37470-42-1 SDS

37470-42-1Synthetic route

2',4'-dihydroxy-4-acetophenone
89-84-9

2',4'-dihydroxy-4-acetophenone

ethyl iodide
75-03-6

ethyl iodide

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

Conditions
ConditionsYield
With potassium carbonate In acetone at 80℃; for 6h;97%
With potassium carbonate In N,N-dimethyl-formamide for 4h;63%
diethyl sulfate
64-67-5

diethyl sulfate

2',4'-dihydroxy-4-acetophenone
89-84-9

2',4'-dihydroxy-4-acetophenone

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

Conditions
ConditionsYield
With potassium carbonate In acetone for 2h; Reflux;78%
In acetone at 20℃; for 25h; Reflux;
ethyl bromide
74-96-4

ethyl bromide

2',4'-dihydroxy-4-acetophenone
89-84-9

2',4'-dihydroxy-4-acetophenone

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

Conditions
ConditionsYield
With potassium carbonate In acetone for 13h; Reflux;73.5%
With potassium carbonate In acetone for 24h; Heating; Yield given;
ethyl bromide
74-96-4

ethyl bromide

2',4'-dihydroxy-4-acetophenone
89-84-9

2',4'-dihydroxy-4-acetophenone

A

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

B

2',4'-dimethoxyacetophenone
829-20-9

2',4'-dimethoxyacetophenone

Conditions
ConditionsYield
With potassium carbonate
2',4'-dihydroxy-4-acetophenone
89-84-9

2',4'-dihydroxy-4-acetophenone

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

Conditions
ConditionsYield
With water; silver nitrate und Erwaermen des erhaltenen Silber-Salzes mit Aethyljodid in Aceton;
7-ethoxy-2-methyl-chromen-4-one
110690-86-3

7-ethoxy-2-methyl-chromen-4-one

sodium ethanolate
141-52-6

sodium ethanolate

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

7-ethoxy-2-ethyl-chromen-4-one

7-ethoxy-2-ethyl-chromen-4-one

sodium ethanolate
141-52-6

sodium ethanolate

A

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

B

propionic acid
802294-64-0

propionic acid

7-ethoxy-2-phenyl-4H-chromen-4-one
93321-62-1

7-ethoxy-2-phenyl-4H-chromen-4-one

sodium ethanolate
141-52-6

sodium ethanolate

A

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

B

benzoic acid
65-85-0

benzoic acid

7-ethoxy-2-benzyl-chromen-4-one

7-ethoxy-2-benzyl-chromen-4-one

sodium ethanolate
141-52-6

sodium ethanolate

A

phenylacetic acid
103-82-2

phenylacetic acid

B

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

7-ethoxy-2-(4-methoxy-phenyl)-chromen-4-one

7-ethoxy-2-(4-methoxy-phenyl)-chromen-4-one

sodium ethanolate
141-52-6

sodium ethanolate

A

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

B

4-methoxybenzoic acid
100-09-4

4-methoxybenzoic acid

7-ethoxy-2-(2-ethoxy-phenyl)-chromen-4-one

7-ethoxy-2-(2-ethoxy-phenyl)-chromen-4-one

sodium ethanolate
141-52-6

sodium ethanolate

A

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

B

4-ethoxy-2-hydroxybenzoic acid
10435-55-9

4-ethoxy-2-hydroxybenzoic acid

C

2-ethoxybenzoic acid
134-11-2

2-ethoxybenzoic acid

7-ethoxy-2-(3-ethoxy-phenyl)-chromen-4-one

7-ethoxy-2-(3-ethoxy-phenyl)-chromen-4-one

sodium ethanolate
141-52-6

sodium ethanolate

A

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

B

3-ethoxybenzoic acid
621-51-2

3-ethoxybenzoic acid

2',4'-dihydroxy-4-acetophenone
89-84-9

2',4'-dihydroxy-4-acetophenone

ethyl iodide
75-03-6

ethyl iodide

A

2′,4′-diethoxyacetophenone
22924-18-1

2′,4′-diethoxyacetophenone

B

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

Conditions
ConditionsYield
With potassium carbonate
2',4'-dihydroxy-4-acetophenone
89-84-9

2',4'-dihydroxy-4-acetophenone

ethyl iodide
75-03-6

ethyl iodide

A

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

B

2',4'-dimethoxyacetophenone
829-20-9

2',4'-dimethoxyacetophenone

Conditions
ConditionsYield
With potassium carbonate
7-ethoxy-2-phenyl-4H-chromen-4-one
93321-62-1

7-ethoxy-2-phenyl-4H-chromen-4-one

A

O-ethyl resorcinol
621-34-1

O-ethyl resorcinol

B

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

C

benzoic acid
65-85-0

benzoic acid

D

carbon dioxid; acetophenone

carbon dioxid; acetophenone

Conditions
ConditionsYield
Kalischmelze;
recorcinol
108-46-3

recorcinol

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

Conditions
ConditionsYield
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
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

5-ethoxy-2-ethyl-phenol

5-ethoxy-2-ethyl-phenol

Conditions
ConditionsYield
With hydrogen; palladium 10% on activated carbon In methanol for 24h;97%
1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

2-(2-acetylphenoxy)-1-bromoethane
52191-14-7

2-(2-acetylphenoxy)-1-bromoethane

1-(2-acetylphenoxy)-2-(2-acetyl-5-ethoxyphenoxy)ethane
635538-05-5

1-(2-acetylphenoxy)-2-(2-acetyl-5-ethoxyphenoxy)ethane

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 80℃;88%
1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

spiro[chromane-2,1'-cyclohexane]-4,4'-dione

spiro[chromane-2,1'-cyclohexane]-4,4'-dione

7-ethoxydispiro[chromane-2,1'-cyclohexane-4',2''-chromane]-4,4''-dione

7-ethoxydispiro[chromane-2,1'-cyclohexane-4',2''-chromane]-4,4''-dione

Conditions
ConditionsYield
With pyrrolidine In ethanol at 80℃; for 10h; Kabe Chromanone Synthesis;85%
morpholine
110-91-8

morpholine

formaldehyd
50-00-0

formaldehyd

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

A

1-[4-ethoxy-2-hydroxy-5-(morpholinomethyl)phenyl]ethanone
1064287-95-1

1-[4-ethoxy-2-hydroxy-5-(morpholinomethyl)phenyl]ethanone

B

1-[4-ethoxy-2-hydroxy-3-(morpholinomethyl)phenyl]ethanone
1064287-96-2

1-[4-ethoxy-2-hydroxy-3-(morpholinomethyl)phenyl]ethanone

Conditions
ConditionsYield
In ethanol; water at 120℃; Mannich reaction;A 83%
B 6%
3-methyl-cyclopentanone
1757-42-2, 6195-92-2

3-methyl-cyclopentanone

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

(1'S,3'R)-7-ethoxy-3'-methylspiro[chroman-2,1'-cyclopentan]-4-one
1069133-20-5

(1'S,3'R)-7-ethoxy-3'-methylspiro[chroman-2,1'-cyclopentan]-4-one

Conditions
ConditionsYield
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
3002-81-1

5, 6-dimethyl-1,10-phenanthroline

terbium(III) nitrate hexahydrate

terbium(III) nitrate hexahydrate

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

Tb(2-hydroxy-4-ethoxyacetophenone)3*5,6-dimethyl-1,10-phenanthroline

Tb(2-hydroxy-4-ethoxyacetophenone)3*5,6-dimethyl-1,10-phenanthroline

Conditions
ConditionsYield
With sodium hydroxide In ethanol at 50 - 55℃; for 0.2h; pH=7 - 8;82%
1-(3,4,5-trimethoxyphenyl)-2-bromoethanone
51490-01-8

1-(3,4,5-trimethoxyphenyl)-2-bromoethanone

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

(6-ethoxy-3-methylbenzofuran-2-yl)(3,4,5-trimethoxyphenyl)methanone
1193107-64-0

(6-ethoxy-3-methylbenzofuran-2-yl)(3,4,5-trimethoxyphenyl)methanone

Conditions
ConditionsYield
With potassium carbonate In acetone for 18h; Reflux;81%
1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

N,N-Dimethylthiocarbamoyl chloride
16420-13-6

N,N-Dimethylthiocarbamoyl chloride

O-2-acetyl-5-ethoxyphenyl N,N-dimethylcarbamothioate
1239890-34-6

O-2-acetyl-5-ethoxyphenyl N,N-dimethylcarbamothioate

Conditions
ConditionsYield
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
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

2-Methylcyclohexanone
583-60-8

2-Methylcyclohexanone

C17H22O3
1069133-30-7

C17H22O3

Conditions
ConditionsYield
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
366-18-7

[2,2]bipyridinyl

terbium(III) nitrate hexahydrate

terbium(III) nitrate hexahydrate

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

Tb(2-hydroxy-4-ethoxyacetophenone)3*2,2-bipyridyl

Tb(2-hydroxy-4-ethoxyacetophenone)3*2,2-bipyridyl

Conditions
ConditionsYield
With sodium hydroxide In ethanol at 50 - 55℃; for 0.2h; pH=7 - 8;79%
3-methyl-cyclopentanone
1757-42-2, 6195-92-2

3-methyl-cyclopentanone

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

C16H20O3
1069133-19-2

C16H20O3

Conditions
ConditionsYield
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
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

benzaldehyde
100-52-7

benzaldehyde

7-ethoxy-2-phenyl-4H-chromen-4-one
93321-62-1

7-ethoxy-2-phenyl-4H-chromen-4-one

Conditions
ConditionsYield
With pyrrolidine; iodine In dimethyl sulfoxide at 150℃; for 12h;78%
N-ethyl-3-carbazolealdehyde
7570-45-8

N-ethyl-3-carbazolealdehyde

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

(E)-1-(4-ethoxy-2-hydroxyphenyl)-3-(9-ethyl-9H-carbazol-3-yl)prop-2-en-1-one

(E)-1-(4-ethoxy-2-hydroxyphenyl)-3-(9-ethyl-9H-carbazol-3-yl)prop-2-en-1-one

Conditions
ConditionsYield
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
66-71-7

1,10-Phenanthroline

terbium(III) nitrate hexahydrate

terbium(III) nitrate hexahydrate

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

Tb(2-hydroxy-4-ethoxyacetophenone)3*1,10-phenanthroline

Tb(2-hydroxy-4-ethoxyacetophenone)3*1,10-phenanthroline

Conditions
ConditionsYield
With sodium hydroxide In ethanol at 50 - 55℃; for 0.2h; pH=7 - 8;78%
1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

2-Methylcyclohexanone
583-60-8

2-Methylcyclohexanone

(1'R,2'S)-7-ethoxy-2'-methylspiro[chroman-2,1'-cyclohexan]-4-one
1069133-29-4

(1'R,2'S)-7-ethoxy-2'-methylspiro[chroman-2,1'-cyclohexan]-4-one

Conditions
ConditionsYield
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%
terbium(III) nitrate hexahydrate

terbium(III) nitrate hexahydrate

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

bathophenanthroline
1662-01-7

bathophenanthroline

Tb(2-hydroxy-4-ethoxyacetophenone)3*bathophenanthroline

Tb(2-hydroxy-4-ethoxyacetophenone)3*bathophenanthroline

Conditions
ConditionsYield
With sodium hydroxide In ethanol at 50 - 55℃; for 0.2h; pH=7 - 8;72%
1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

(carbethoxyethylidene)triphenylphosphorane
21382-82-1

(carbethoxyethylidene)triphenylphosphorane

7-ethoxy-3,4-dimethyl-coumarin
111244-98-5

7-ethoxy-3,4-dimethyl-coumarin

Conditions
ConditionsYield
at 180℃; for 10h;66%
1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

6-ethoxy-7-iodobenzo[d]oxazol-2(3H)-one

6-ethoxy-7-iodobenzo[d]oxazol-2(3H)-one

Conditions
ConditionsYield
With sodium azide; iodine; sodium hydrogencarbonate In N,N-dimethyl-formamide at 100℃; for 2h;66%
terbium(III) nitrate hexahydrate

terbium(III) nitrate hexahydrate

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

water
7732-18-5

water

Tb(2-hydroxy-4-ethoxyacetophenone)3*2H2O

Tb(2-hydroxy-4-ethoxyacetophenone)3*2H2O

Conditions
ConditionsYield
With sodium hydroxide In ethanol at 50 - 55℃; for 0.2h; pH=7 - 8;65%
thiophene-2-carbaldehyde
98-03-3

thiophene-2-carbaldehyde

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

7-ethoxy-3-hydroxy-2-(thiophen-2-yl)-4H-chromen-4-one
1364733-90-3

7-ethoxy-3-hydroxy-2-(thiophen-2-yl)-4H-chromen-4-one

Conditions
ConditionsYield
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
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

2,2-diazido-6-ethoxy-5,7-diiodobenzofuran-3(2H)-one

2,2-diazido-6-ethoxy-5,7-diiodobenzofuran-3(2H)-one

Conditions
ConditionsYield
With sodium azide; iodine; sodium hydrogencarbonate In water at 100℃; for 2h;54%
benzothiophene-3-carboxaldehyde
5381-20-4

benzothiophene-3-carboxaldehyde

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

(E)-3-(benzo[b]thiophen-3-yl)-1-(4-ethoxy-2-hydroxyphenyl)prop-2-en-1-one

(E)-3-(benzo[b]thiophen-3-yl)-1-(4-ethoxy-2-hydroxyphenyl)prop-2-en-1-one

Conditions
ConditionsYield
With sodium hydroxide In ethanol; water at 20℃; Claisen-Schmidt Condensation;52%
morpholine
110-91-8

morpholine

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

2-(4-ethoxy-2-hydroxyphenyl)-1-morpholinoethanethione

2-(4-ethoxy-2-hydroxyphenyl)-1-morpholinoethanethione

Conditions
ConditionsYield
With sulfur at 130℃; for 16h;52%
1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

benzaldehyde
100-52-7

benzaldehyde

7-ethoxy-3-hydroxy-2-phenyl-4H-chromen-4-one

7-ethoxy-3-hydroxy-2-phenyl-4H-chromen-4-one

Conditions
ConditionsYield
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
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

4-formylphenylboronic acid,
87199-17-5

4-formylphenylboronic acid,

7-ethoxy-3-hydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one
1364733-22-1

7-ethoxy-3-hydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one

Conditions
ConditionsYield
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
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

benzaldehyde
100-52-7

benzaldehyde

4'-ethoxy-2'-hydroxy-trans-chalcone
70668-35-8

4'-ethoxy-2'-hydroxy-trans-chalcone

Conditions
ConditionsYield
With potassium hydroxide In methanol; water at 20℃; for 24h; Aldol Condensation;20%
carbon disulfide
75-15-0

carbon disulfide

1-(4-ethoxy-2-hydroxyphenyl)ethanone
37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

7-Ethoxy-4-hydroxy-2H-1-benzopyran-2-thione
173210-12-3

7-Ethoxy-4-hydroxy-2H-1-benzopyran-2-thione

Conditions
ConditionsYield
With potassium tert-butylate In benzene Ambient temperature;18%

37470-42-1Relevant articles and documents

Photoluminescence performance of green light emitting terbium (III) complexes with β-hydroxy ketone and nitrogen donor ancillary ligands

Khanagwal, Jyoti,Kumar, Rajesh,Devi, Rekha,Bala, Manju,Sehrawat, Priyanka,Khatkar,Taxak

, p. 742 - 754 (2021)

An efficient and cost-effective technique, solution precipitation approach is adopted to synthesize five bright green luminescent terbium (III) complexes by employing the main β-hydroxy ketone ligand, 2-hydroxy-4-ethoxyacetophenone, and ancillary ligands like bathophenanthroline, 5,6-dimethyl-1,10-phenanthroline, 1,10-phenanthroline, and 2,2-bipyridyl. The elemental compositions and binding mode of ligand to terbium (III) ion can be validated by using energy dispersive X-ray analysis, elemental analysis, Fourier transform infrared, and proton nuclear magnetic resonance spectroscopy. The complexes are thermally stable up to 158°C and possess the cubic shaped particles as confirmed by thermogravimetric analysis and scanning electron microscopic study, respectively. The band-gap energy (3.02–2.92 eV) of complexes is reckoned through diffuse reflectance spectra, which tailors them as potential candidates in the field of military radars. The photoluminescence studies unveil that the complexes exhibit the bright green luminescence corresponding to 5D4 → 7F5 transition of Tb3+ ion (548 nm) under the excitation wavelength of 395 or 397 nm. The Commission International de I’Eclairage chromaticity coordinates (x, y) and color purity substantiates the green emission of complexes. The energy transfer mechanism elucidates that the main ligand and ancillary ligands sensitize Tb3+ ion, which in turn enhances the luminescence efficiency of the emissive layer of white organic light emitting diodes. The results reveal that the complexes are considered as good contenders in the field of display devices and laser technology. Lastly, in vitro antimicrobial and antioxidant activity proclaim the potent antimicrobial and antioxidant actions of complexes via tube dilution and 2, 2-diphenyl-1-picrylhydrazyl assays, respectively.

Designing of luminescent complexes of europium(III) ion with hydroxyl ketone and nitrogen donor secondary ligands for improving the luminescence performance and biological actions

Hooda, Pooja,Khanagwal, Jyoti,Khatkar, S. P.,Kumar, Rajesh,Poonam,Taxak, V. B.

, (2021)

Europium based five luminescent europium(III) complexes with 2-hydroxy-4-ethoxyacetophenone (main ligand) and second chromophores, bathophenanthroline, 5,6-dimethyl-1,10-phenanthroline, 1,10-phenanthroline and 2,2-bipyridyl have been prepared by employing cost-effective solution precipitation method. The various advanced techniques are employed to investigate the structural information. Thermal study proclaims the thermal stability of complexes up to 155 °C. The analyzed band-gap for complexes opens the application of these complexes in laser system. The photoluminescent properties of complexes under ultraviolet light clearly reveal the presence of prominent emission peak (5D0→7F2 transition) centered at 611 nm responsible for intense red emission of complexes, which highlights the applicability of these complexes in advanced optoelectronic devices. Judd-Ofelt intensity parameters, internal quantum efficiency and sensitization mechanism confirm the luminescence efficiency of complexes. The complexes display the excellent antimicrobial and antioxidant features.

Natural product Hirtellanine B and its derivatives in the preparation process for the preparation of medicine for treating tumor with the application of the

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Paragraph 0065; 0150, (2016/10/10)

The present invention provides a preparation method of a natural product Hirtellanine B, wherein 2,4,6-trihydroxyacetophenone is adopted as a raw material, and steps of compound a preparation, compound b preparation, compound c preparation, compound d preparation, compound e preparation, compound f preparation, compound g preparation, and the like are performed to prepare the natural product Hirtellanine B. According to the present invention, biological activity screening is performed on Hirtellanine B and 14 Hirtellanine B derivatives, and results show that the natural product Hirtellanine B can inhibit proliferations of Jurkat cells, Raji cells and K562 cells, and the compounds provide a certain inhibition activity for tumor cells. The method has characteristics of easily available raw material, high reaction yield and reasonable operation, and is suitable for industrial production. The Hirtellanine B and the derivatives thereof can be used for preparing tumor treatment drugs, and have great clinical values. The natural product Hirtellanine B preparation method reaction formulas are as the follows.

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