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46118-95-0

46118-95-0

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46118-95-0 Usage

Chemical Properties

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Check Digit Verification of cas no

The CAS Registry Mumber 46118-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,1,1 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 46118-95:
(7*4)+(6*6)+(5*1)+(4*1)+(3*8)+(2*9)+(1*5)=120
120 % 10 = 0
So 46118-95-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2S/c1-5-2-3-8-7(9-5)12-4-6(10)11/h2-3H,4H2,1H3,(H,10,11)/p-1

46118-95-0 Well-known Company Product Price

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  • Alfa Aesar

  • (L06671)  2-Carboxymethylthio-4-methylpyrimidine, 98%   

  • 46118-95-0

  • 5g

  • 547.0CNY

  • Detail

  • Alfa Aesar

  • (L06671)  2-Carboxymethylthio-4-methylpyrimidine, 98%   

  • 46118-95-0

  • 25g

  • 1728.0CNY

  • Detail

46118-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methylpyrimidin-2-yl)sulfanylacetic acid

1.2 Other means of identification

Product number -
Other names 2-Carboxymethylmercapto-4-methyl-pyrimidin

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:46118-95-0 SDS

46118-95-0Downstream Products

46118-95-0Relevant articles and documents

Regioselective reaction: Synthesis of novel Mannich bases derived from 3-(4,6-disubstituted-2-thiomethylpyrimidyl)-4-amino-5-mercapto-1,2-4-triazoles and their antimicrobial properties

Lingappa,Girisha,Kalluraya, Balakrishna,Satheesh Rai,Kumari, Nalilu Suchetha

body text, p. 1858 - 1864 (2009/05/26)

A new series of 3-(4,6-disubstituted-2-thiomethylpyrimidyl)-4-amino-5- mercapto-1,2-4-triazoles have been synthesized. These triazoles on reaction with aldehydes in the presence of acid catalyst forms Schiff's bases. These Schiff's bases can exist both in the thiol as well as in the thione tautomeric form. However when these compounds are subjected to Mannich reaction, M-Mannicli bases 7a-f are obtained rather than the S-Mannich bases. The structures of the new compounds have been confirmed by spectral and analytical data. Few of these Mannich bases have been evaluated for their possible antifungal and antibacterial activity. Most of the tested compounds show significant antifungal and antibacterial activity.

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