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783370-96-7

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783370-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 783370-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,3,3,7 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 783370-96:
(8*7)+(7*8)+(6*3)+(5*3)+(4*7)+(3*0)+(2*9)+(1*6)=197
197 % 10 = 7
So 783370-96-7 is a valid CAS Registry Number.

783370-96-7SDS

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 2-hydroxy-4-methoxy-N-(6-methylpyridin-2-yl)benzamide

1.2 Other means of identification

Product number -
Other names -

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:783370-96-7 SDS

783370-96-7Downstream Products

783370-96-7Relevant articles and documents

Antimycobacterial N-pyridinylsalicylamides, isosters of salicylamides

Waisser, Karel,Drazkova, Katerina,Kunes, Jiri,Klimesova, Vera,Kaustova, Jarmila

, p. 615 - 625 (2007/10/03)

The series of derivatives of substituted N-pyridinylsalicylamides were synthesized. The compounds were evaluated for in vitro antimycobacterial activity against Mycobacterium avium and two strains of Mycobacterium kansasii. In the quantitative structure activity relationships analysis (QSAR), the Free-Wilson and Hansch approaches were used but the analysis was not significant. (The standard deviations of regression coefficients were greater than the values of the coefficients). The molecules were separated the heterocyclic and salicyl moiety in the molecules, and the study of influences of substituents on salicyl moiety was used, as well. 5-Chloro-pyridin-2-yl, and the substitution of the salicyl moiety by chlorine in position 4 or 5 had the strongest influence on the increase in antimycobacterial activity.

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