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Benzenepropanamide, 3-methyl-β-oxo-N-phenyl-, also known as 3-methyl-N-phenyl-β-oxobenzenepropanamide, is a chemical compound with the molecular formula C16H15NO2. It is a derivative of benzenepropanamide, featuring a methyl group at the 3-position, a carbonyl group at the β-position, and a phenyl group attached to the nitrogen atom. Benzenepropanamide, 3-methyl-b-oxo-N-phenyl- is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other antidepressant medications. Its structure and properties make it a versatile building block in organic chemistry, allowing for further functionalization and modification to create a wide range of compounds with diverse applications.

962-01-6

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962-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 962-01-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,6 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 962-01:
(5*9)+(4*6)+(3*2)+(2*0)+(1*1)=76
76 % 10 = 6
So 962-01-6 is a valid CAS Registry Number.

962-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methyl-benzoylessigsaeure-anilid

1.2 Other means of identification

Product number -
Other names m-Methylbenzoylacetanilid

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:962-01-6 SDS

962-01-6Relevant academic research and scientific papers

Highly enantioselective epoxidation catalyzed by cinchona thioureas: Synthesis of functionalized terminal epoxides bearing a quaternary stereogenic center

Russo, Alessio,Galdi, Gerardina,Croce, Gianluca,Lattanzi, Alessandra

supporting information; experimental part, p. 6152 - 6157 (2012/06/30)

A brilliant debut! Cinchona thioureas have been reported for the first time as catalysts in the area of asymmetric oxidations. They efficiently promote an unprecedented highly enantioselective epoxidation of deactivated 1,1-disubstituted alkenes to terminal epoxides containing a quaternary stereogenic center (see scheme). Copyright

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