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3-methyl-4-phenylcyclohex-2-en-1-one is a chemical compound with the molecular formula C15H16O. It is a derivative of cyclohexenone, featuring a methyl group at the 3rd carbon and a phenyl group at the 4th carbon. 3-methyl-4-phenylcyclohex-2-en-1-one is an organic molecule that belongs to the class of aromatic ketones, characterized by the presence of a carbonyl group (C=O) and a benzene ring. It is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in organic chemistry. The compound's structure provides it with unique chemical properties, making it a valuable component in the development of new compounds with specific functionalities.

6312-13-6

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6312-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6312-13-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6312-13:
(6*6)+(5*3)+(4*1)+(3*2)+(2*1)+(1*3)=66
66 % 10 = 6
So 6312-13-6 is a valid CAS Registry Number.

6312-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-4-phenylcyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3-Methyl-4-phenyl-cyclohex-2-enon

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

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More Details:6312-13-6 SDS

6312-13-6Relevant academic research and scientific papers

One-pot β-substitution of enones with alkyl groups to β-alkyl enones

Matsuo, Jun-Ichi,Aizawa, Yayoi

, p. 2399 - 2401 (2007/10/03)

Vinylic hydrogens at the β-position of enones were effectively substituted with alkyl groups in a one-pot procedure to afford β-alkyl enones in good to high isolated yields by conjugate addition of higher-order dialkyl cyanocuprates to enones, followed by a reaction with N-tert-butylbenzenesulfinimidoyl chloride at -78 °C. The Royal Society of Chemistry 2005.

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