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(3,4-dimethylphenyl)(4-methylphenyl)methanone is a chemical compound with the molecular formula C16H16O. It is a ketone compound that consists of two aromatic rings, one with a 3,4-dimethyl substituent and the other with a 4-methyl substituent, attached to a carbonyl group.

24964-78-1

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24964-78-1 Usage

Uses

Used in Organic Synthesis:
(3,4-dimethylphenyl)(4-methylphenyl)methanone is used as a building block in organic synthesis for the creation of various chemical compounds.
Used in Pharmaceutical Research:
(3,4-dimethylphenyl)(4-methylphenyl)methanone is used as a research compound in pharmaceutical research due to its potential biological activities and its investigation for use as a psychoactive substance.
Used in Fragrance and Flavoring Production:
(3,4-dimethylphenyl)(4-methylphenyl)methanone is used as an ingredient in the production of fragrances and flavorings due to its aromatic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 24964-78-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,6 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24964-78:
(7*2)+(6*4)+(5*9)+(4*6)+(3*4)+(2*7)+(1*8)=141
141 % 10 = 1
So 24964-78-1 is a valid CAS Registry Number.

24964-78-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,4-dimethylphenyl)-(4-methylphenyl)methanone

1.2 Other means of identification

Product number -
Other names 3,4,4'-Trimethyl-benzophenon

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:24964-78-1 SDS

24964-78-1Downstream Products

24964-78-1Relevant academic research and scientific papers

Synthesis of Diverse Aromatic Ketones through C?F Cleavage of Trifluoromethyl Group

Ikeda, Mai,Matsuzawa, Tsubasa,Morita, Takamoto,Hosoya, Takamitsu,Yoshida, Suguru

supporting information, p. 12333 - 12337 (2020/09/09)

An efficient synthetic method of aromatic ketones through C?F cleavage of trifluoromethyl group is disclosed. The high functional group tolerance of the transformation and the remarkable stability of trifluoromethyl group in various reactions enabled mult

Synthesis of fluorenone derivatives through Pd-catalyzed dehydrogenative cyclization

Li, Hu,Zhu, Ru-Yi,Shi, Wen-Juan,He, Ke-Han,Shi, Zhang-Jie

, p. 4850 - 4853,4 (2012/12/12)

Palladium-catalyzed dual C-H functionalization of benzophenones to form fluorenones by oxidative dehydrogenative cyclization is reported. This method provides a concise and effective route toward the synthesis of fluorenone derivatives, which shows outstanding functional group compatibility.

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