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55749-30-9

55749-30-9

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55749-30-9 Usage

Chemical Properties

OFF-WHITE CRYSTALLINE POWDER

Check Digit Verification of cas no

The CAS Registry Mumber 55749-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,4 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55749-30:
(7*5)+(6*5)+(5*7)+(4*4)+(3*9)+(2*3)+(1*0)=149
149 % 10 = 9
So 55749-30-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O2S/c1-5-3-6(2)10-8(9-5)13-4-7(11)12/h3H,4H2,1-2H3,(H,11,12)/p-1

55749-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4,6-dimethylpyrimidin-2-yl)sulfanylacetic acid

1.2 Other means of identification

Product number -
Other names (4,6-Dimethyl-2-pyrimidinylthio)acetic 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:55749-30-9 SDS

55749-30-9Downstream Products

55749-30-9Relevant 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.

Synthesis of N-substituted 3-nitrophthalimides

Zav'yalov,Dorofeeva,Rumyantseva,Kulikova,Ezhova,Kravchenko,Zavozin

, p. 154 - 156 (2007/10/03)

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