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98436-74-9

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98436-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98436-74-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,4,3 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 98436-74:
(7*9)+(6*8)+(5*4)+(4*3)+(3*6)+(2*7)+(1*4)=179
179 % 10 = 9
So 98436-74-9 is a valid CAS Registry Number.

98436-74-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethenylpyridine-4-carbonitrile

1.2 Other means of identification

Product number -
Other names G-5027

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:98436-74-9 SDS

98436-74-9Downstream Products

98436-74-9Relevant articles and documents

Mur ligases inhibitors with azastilbene scaffold: Expanding the structure–activity relationship

Hrast, Martina,Frlan, Rok,Knez, Damijan,Zdovc, Irena,Barreteau, Hélène,Gobec, Stanislav

supporting information, (2021/05/10)

Antibiotic resistance represents one of the biggest public health challenges in the last few years. Mur ligases (MurC–MurF) are involved in the synthesis of UDP-N-acetylmuramyl-pentapeptide, the main building block of bacterial peptidoglycan polymer. They are essential for the survival of bacteria and therefore important antibacterial targets. We report herein the synthesis and structure–activity relationships of Mur ligases inhibitors with an azastilbene scaffold. Several compounds showed promising inhibitory potencies against multiple ligases and one compound also possessed moderate antibacterial activity. These results represent a solid ground for further development and optimization of structurally novel antimicrobial agents to combat the rising bacterial resistance.

METABOTROPIC GLUTAMATE RECEPTOR 5 MODULATORS AND METHODS OF USE THEREOF

-

Page/Page column 80, (2013/02/27)

Compounds that modulate GluR5 activity and methods of using the same are disclosed.

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