1-(4-Benzylphenyl)ethan-1-one

1-(4-Benzylphenyl)ethan-1-one - Names and Identifiers

Name	(4-ACETYLPHENYL)PHENYLMETHANE
Synonyms	AKOS BBS-00000790 4-ACETYLDIPHENYLMETHANE 1-(4-Benzylphenyl)ethanone 1-(4-Benzylphenyl)ethan-1-one (4-ACETYLPHENYL)PHENYLMETHANE Ethanone, 1-[4-(phenylmethyl)phenyl]- 4-Acetyldiphenylmethane, 4-Benzylacetophenone
CAS	782-92-3

1-(4-Benzylphenyl)ethan-1-one - Physico-chemical Properties

Molecular Formula	C15H14O
Molar Mass	210.27
Density	1.049±0.06 g/cm3(Predicted)
Melting Point	38 °C
Boling Point	188-190 °C(Press: 5 Torr)
Storage Condition	Room Temprature

1-(4-Benzylphenyl)ethan-1-one - Risk and Safety

Hazard Symbols

Xi - Irritant

1-(4-Benzylphenyl)ethan-1-one - Upstream Downstream Industry

Raw Materials	Ethanone, 1-(4-acetylphenyl)-2-phenyl- Pyridine, 2-[dimethyl(phenylmethyl)silyl]- dimethyl-carbamic acid benzyl ester 1-[4-(chloromethyl)phenyl]ethanone 4-ACETYLPHENYLBORONIC ACID, PINACOL ESTER Triphenylbismuth 4-Iodoacetophenone 4-Acetylphenylboronic acid 4-ACETYLPHENYL TRIFLATE BENZALDEHYDE TOSYLHYDRAZONE Diphenylmethane Benzyl chloride carbon monoxide
Downstream Products	2-Phenylpyridine

1-(4-Benzylphenyl)ethan-1-one - Introduction

(4-ACETYLPHENYL) phenmethyl, chemical formula C15H14O, is an organic compound. The following is a description of its nature, use, formulation and safety information:

Nature:
-Appearance: White crystalline solid.
-Melting point: About 80-82 degrees Celsius.
-Solubility: Soluble in organic solvents such as alcohols, ethers and chlorinated hydrocarbons.
-Chemical properties: It can be used as a ketone compound, which is reduced to the corresponding alcohol through the ketone reduction reaction.

Use:
- (4-ACETYLPHENYL)PHENYLMETHANE can be used as a raw material and intermediate in organic synthesis.
-In the field of medicine, it may have anti-inflammatory and antibacterial activities and can be used to synthesize drugs.
-Due to its special chemical structure, it can also be used in the synthesis of dyes and fragrances.

Method: The synthesis of
(4-ACETYLPHENYL) phenmethyl is usually completed by acyl transfer reaction, and the specific steps include:
1. Under alkaline conditions, benzoic acid is reacted with acetic anhydride to obtain acetyl benzoic acid.
2. Acetobenzoic acid reacts with methyl bromide to generate (4-ACETYLPHENYL)PHENYLMETHANE.

Safety Information:
There are limited toxicological data on (4-ACETYLPHENYL) phenmethylane, but there are no reports indicating that it has a special risk of harm to human health. However, as a chemical, care should be taken to follow proper laboratory procedures and avoid skin contact and inhalation. In case of accidental contact, rinse immediately with plenty of water and seek medical help. Relevant safety standards and guidelines should be followed during storage and handling.

Last Update：2024-04-09 21:04:16