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113708-04-6

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113708-04-6 Usage

General Description

4-Pyridinecarboxamide, 2,6-dimethyl (9CI) is a chemical compound with the molecular formula C8H10N2O. It is also known by its IUPAC name, 2,6-dimethylnicotinamide. 4-Pyridinecarboxamide,2,6-dimethyl-(9CI) is a derivative of nicotinamide, and it is used in the synthesis of pharmaceuticals. It has been found to have various pharmacological properties including anti-inflammatory, anti-tumor, and anti-microbial activities. Additionally, 4-Pyridinecarboxamide, 2,6-dimethyl (9CI) has shown potential in the treatment of neurodegenerative disorders such as Alzheimer's disease and Parkinson's disease. This chemical compound is a valuable tool in medicinal chemistry research and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 113708-04-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,0 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 113708-04:
(8*1)+(7*1)+(6*3)+(5*7)+(4*0)+(3*8)+(2*0)+(1*4)=96
96 % 10 = 6
So 113708-04-6 is a valid CAS Registry Number.

113708-04-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Dimethylisonicotinamide

1.2 Other means of identification

Product number -
Other names 2,6-dimethyl-4-chloropyridine

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:113708-04-6 SDS

113708-04-6Relevant articles and documents

LTA4 Hydrolase inhibitors

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Page 41, 203, (2010/01/31)

The present invention provides compounds of the formula Ar1-Q-Ar2-Y-R-Z and pharmaceutically acceptable salts thereof wherein Ar1 and Ar2 are optionally substituted aryl moieties, Z is an optionally substituted nitrogen-containing moiety which may be an acyclic, cyclic or bicyclic amine or an optionally substituted monocyclic or bicyclic nitrogen-containing heteroaromatic moiety; Q is a linking group capable of linking two aryl groups; R is an alkylene moiety; Y is a linking moiety capable of linking an aryl group to an alkylene moiety and wherein Z is bonded to R through a nitrogen atom. The compounds and pharmaceutical compositions of the present invention are useful in the treatment of inflammatory diseases which are mediated by LTB4 production, such as proriasis, ulcerative colitis, IBD and asthma.

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