(E)-1-(4-(苄氧基)-2-羟基苯基)-3-(2-甲氧基-4-甲基苯基)丙-2-烯-1-酮
(E)-1-(4-(Benzyloxy)-2-hydroxyphenyl)-3-(2-methoxy-4-methylphenyl)prop-2-en-1-one
CAS: 1218900-66-3
Molecular Formula: C24H22O4
(E)-1-(4-(苄氧基)-2-羟基苯基)-3-(2-甲氧基-4-甲基苯基)丙-2-烯-1-酮 - Names and Identifiers
(E)-1-(4-(苄氧基)-2-羟基苯基)-3-(2-甲氧基-4-甲基苯基)丙-2-烯-1-酮 - Physico-chemical Properties
| Molecular Formula | C24H22O4 |
| Molar Mass | 374.43 |
| Storage Condition | 2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD18071028 |
(E)-1-(4-(苄氧基)-2-羟基苯基)-3-(2-甲氧基-4-甲基苯基)丙-2-烯-1-酮 - Introduction
(E)-1-(4-(Benzyloxy)-2-hydroxyphenyl)-3-(2-methoxy-4-methylphenyl)prop-2-en-1-one is an organic compound with the chemical formula C24H22O4. Its structure contains benzyl, hydroxyl, methoxy and methyl phenyl groups.
This compound is mainly used in scientific research experiments, for example, as an intermediate in drug synthesis or as a starting material for drug research.
The method of preparing this compound is through a multi-step synthesis. First, an intermediate of anisole benzyl alcohol was prepared from anisole and p-benzyl alcohol. Then, anisole benzylic acid was obtained by etherification reaction under acid catalysis. Next, anisole hydroxylamine was obtained by diazotization-dediazotization reduction. Finally, the target compound is prepared by addition and ketonization with methoxymethylaniline.
Regarding safety information, since the specific toxicity and danger of the compound have not been reported in detail, it is necessary to follow laboratory safety practices and wear appropriate personal protective equipment when used. Avoid contact with skin, eyes and inhalation during handling and storage. If careless contact, please timely cleaning. If discomfort occurs, immediate medical attention is recommended.
This compound is mainly used in scientific research experiments, for example, as an intermediate in drug synthesis or as a starting material for drug research.
The method of preparing this compound is through a multi-step synthesis. First, an intermediate of anisole benzyl alcohol was prepared from anisole and p-benzyl alcohol. Then, anisole benzylic acid was obtained by etherification reaction under acid catalysis. Next, anisole hydroxylamine was obtained by diazotization-dediazotization reduction. Finally, the target compound is prepared by addition and ketonization with methoxymethylaniline.
Regarding safety information, since the specific toxicity and danger of the compound have not been reported in detail, it is necessary to follow laboratory safety practices and wear appropriate personal protective equipment when used. Avoid contact with skin, eyes and inhalation during handling and storage. If careless contact, please timely cleaning. If discomfort occurs, immediate medical attention is recommended.
Last Update：2024-04-09 21:04:16
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(E)-1-(4-(苄氧基)-2-羟基苯基)-3-(2-甲氧基-4-甲基苯基)丙-2-烯-1-酮
(RS)-4-[3-甲氨基-1-(2-噻吩基)丙基]-1-萘酚
(3-Aminophenyl) -Urea
5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-7-methyl-(9CI)
(+)-PICFELTARRAENIN IA
2-氨基-4-氯-6-氧代-1,6-二氢嘧啶-5-甲腈
Butanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-3-hydroxy-, (S)- (9CI)
γ-(2-Hydroxy-phenyl)-buttersaeure-aethylester
Trichoplein keratin filament-binding protein
2-乙基-4-嘧啶甲醛
(RS)-4-[3-甲氨基-1-(2-噻吩基)丙基]-1-萘酚
(3-Aminophenyl) -Urea
5H-Cyclopenta[c]pyridin-5-one,6,7-dihydro-7-methyl-(9CI)
(+)-PICFELTARRAENIN IA
2-氨基-4-氯-6-氧代-1,6-二氢嘧啶-5-甲腈
Butanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-3-hydroxy-, (S)- (9CI)
γ-(2-Hydroxy-phenyl)-buttersaeure-aethylester
Trichoplein keratin filament-binding protein
2-乙基-4-嘧啶甲醛