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4332-79-0

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4332-79-0 Usage

General Description

1-Benzyl-6-oxo-1,6-dihydro-3-pyridinecarboxylic acid is a chemical compound with the molecular formula C16H15NO3. It is a derivative of pyridine with a benzyl group and a carboxylic acid group. 1-BENZYL-6-OXO-1,6-DIHYDRO-3-PYRIDINECARBOXYLIC ACID is used in the pharmaceutical industry as an intermediate for the synthesis of various drugs and pharmaceutical products. It has potential applications in the development of new medications for a variety of medical conditions. The compound's structure and properties make it a valuable building block for the synthesis of diverse molecules with potential biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 4332-79-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,3 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4332-79:
(6*4)+(5*3)+(4*3)+(3*2)+(2*7)+(1*9)=80
80 % 10 = 0
So 4332-79-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H11NO3/c15-12-7-6-11(13(16)17)9-14(12)8-10-4-2-1-3-5-10/h1-7,9H,8H2,(H,16,17)

4332-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-6-oxopyridine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names F2143-0001

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:4332-79-0 SDS

4332-79-0Relevant articles and documents

Synthesis and reduction reactions of pyridones and 5-acyl-2-methoxypyridines

Bisset, Alexander A.,Dishington, Allan,Jones, Teyrnon,Clarkson, Guy J.,Wills, Martin

, p. 7207 - 7220 (2017/09/12)

The synthesis of a series of pyridones, from their 2-hydroxypyridine or 2-methoxypyridine precursors, is described, along with studies into their reductions to saturated heterocycles. A number of 5-acylpyridones were prepared and were evaluated as substrates for asymmetric transfer hydrogenation prior to conversion to saturated heterocycles. The enantioselective reduction of 5-acetyl-1-benzylpyrimidine-2,4(1H,3H)-dione is also described.

Imination of N-methylpyridinium salts by liquid ammonia-potassium permanganate [1]. A new synthesis of nudiflorine

Buurman,Van der Plas

, p. 1015 - 1018 (2007/10/02)

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