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5308-12-3

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5308-12-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5308-12-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,0 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5308-12:
(6*5)+(5*3)+(4*0)+(3*8)+(2*1)+(1*2)=73
73 % 10 = 3
So 5308-12-3 is a valid CAS Registry Number.

5308-12-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name O-ethyl N-(4-methylphenyl)carbamothioate

1.2 Other means of identification

Product number -
Other names p-Tolyl-thiocarbamidsaeure-O-aethylester

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:5308-12-3 SDS

5308-12-3Relevant articles and documents

Pathogenic Gram-positive bacteria are highly sensitive to triphenylphosphanegold(O-alkylthiocarbamates), Ph3PAu[SC(OR)=N(p- tolyl)] (R = Me, et and iPr)

Yeo, Chien Ing,Sim, Jiun-Horng,Khoo, Chai-Hoon,Goh, Zheng-Jie,Ang, Kok-Pian,Cheah, Yoke-Kqueen,Fairuz, Zainal Abidin,Halim, Siti Nadiah Binti Abdul,Ng, Seik Weng,Seng, Hoi-Ling,Tiekink, Edward R. T.

, p. 145 - 152 (2013/10/22)

The phosphanegold(I) thiocarbamides, Ph3PAu{SC(OR)=NC 6H4Me-4} for R = Me (1), Et (2) and iPr (3), have been shown to have essentially linear gold atom coordination geometries defined by phosphane-P and thiolate-S atoms, and exhibit minimum inhibitory concentration (MIC) values in the range of 1-37 μg/ml against four Gram-positive bacteria, namely Bacillus cereus, Enterococcus faecalis, Enterococcus faecium and Staphylococcus aureus; compounds 1-3 are less potent against a broad panel of 16 Gram-negative bacteria. As the minimum bactericidal concentration values were quite similar to the MIC values, compounds 1-3 are effective bactericidal agents. The specific action against the four Gram-positive bacteria suggests they function by inhibition of peptidoglycan synthesis.

3,4-diarylthiazolin-2-one or -2-thione derivatives, their methods of preparation and their uses in their methods of preparation and their uses in therapeutics

-

, (2008/06/13)

The present invention relates to derivatives of formula STR1 and to their use in therapeutics especially as drugs with anti-inflammatory and analgesic properties.

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