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180790-90-3

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180790-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180790-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,7,9 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 180790-90:
(8*1)+(7*8)+(6*0)+(5*7)+(4*9)+(3*0)+(2*9)+(1*0)=153
153 % 10 = 3
So 180790-90-3 is a valid CAS Registry Number.

180790-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Methylsulfanyl)isonicotinonitrile

1.2 Other means of identification

Product number -
Other names 2-methylthiopyridine-3-carboxylic acid

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:180790-90-3 SDS

180790-90-3Upstream product

180790-90-3Downstream Products

180790-90-3Relevant articles and documents

Potential antifungal agents. Synthesis and activity of 2-alkylthiopyridine-4-carbothioamides

Klimesova,Otcenasek,Waisser

, p. 389 - 395 (1996)

A series of 2-alkylthiopyridine-4-carbothioamides were synthesized, and their antifungal potency was tested. The chemical structures were proved by IR and 1H-NMR data and by elemental analysis. The MIC and MFC assessment were used for the estimation of potential activity in vitro. The study comprising 21 clinical isolates of fungi showed that compounds 5h and 5j exhibited fair inhibitory activity against some yeasts and dermatophytes. Selective fungistatic activity against dermatophytes (MIC = 3.12-25.0 μg/mL) was found also in compound 5g. None of the above compounds showed inhibitory activity against non-dermatophyte filamentous fungi. Microbiological activity of 2-alkylthiopyridine-4-carbothioamides appears to be mainly related to hydrophobicity of alkyl in position 2.

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