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N-(4-Methyl-pyridin-3-yl)-benzamide is a chemical compound with the molecular formula C13H12N2O. It is a derivative of benzamide, where a 4-methyl-pyridin-3-yl group is attached to the nitrogen atom. N-(4-METHYL-PYRIDIN-3-YL)-BENZAMIDE is known for its potential applications in medicinal chemistry, particularly as a building block for the synthesis of various pharmaceuticals and agrochemicals. It is characterized by its white crystalline appearance and is often used in research and development for the creation of new compounds with specific biological activities. The compound's structure allows for further functionalization and modification, making it a versatile intermediate in organic synthesis.

2922-05-6

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2922-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2922-05-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,2 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2922-05:
(6*2)+(5*9)+(4*2)+(3*2)+(2*0)+(1*5)=76
76 % 10 = 6
So 2922-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N2O/c1-10-7-8-14-9-12(10)15-13(16)11-5-3-2-4-6-11/h2-9H,1H3,(H,15,16)

2922-05-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-methylpyridin-3-yl)benzamide

1.2 Other means of identification

Product number -
Other names Benzamide,N-(4-methyl-3-pyridinyl)

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:2922-05-6 SDS

2922-05-6Downstream Products

2922-05-6Relevant academic research and scientific papers

A novel one-step synthesis of 2-substituted 6-azaindoles from 3-amino-4-picoline and carboxylic esters

Song, Jinhua J.,Tan, Zhulin,Gallou, Fabrice,Xu, Jinghua,Yee, Nathan K.,Senanayake, Chris H.

, p. 6512 - 6514 (2007/10/03)

Dilithiation of 3-amino-4-picoline (1) was achieved with sec-BuLi at room temperature. Condensation of the resulting dianion (2) with carboxylic esters afforded a wide range of 2-substituted 6-azaindoles in good yields.

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