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1074-41-5

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1074-41-5 Usage

Chemical Properties

4-AMINO-2-(METHYLTHIO)-6-PYRIMIDINOL is White Solid

Uses

Different sources of media describe the Uses of 1074-41-5 differently. You can refer to the following data:
1. 4-AMINO-2-(METHYLTHIO)-6-PYRIMIDINOL is a useful synthetic intermediate
2. Intermediate in the preparation of certain antibiotics

Check Digit Verification of cas no

The CAS Registry Mumber 1074-41-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1074-41:
(6*1)+(5*0)+(4*7)+(3*4)+(2*4)+(1*1)=55
55 % 10 = 5
So 1074-41-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H7N3OS/c1-10-5-7-3(6)2-4(9)8-5/h2H,1H3,(H3,6,7,8,9)

1074-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Amino-2-(Methylthio)-6-Pyrimidinol

1.2 Other means of identification

Product number -
Other names 6-Amino-2-(methylsulfanyl)-4(3H)-pyrimidinone

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:1074-41-5 SDS

1074-41-5Relevant articles and documents

Synthesis of novel 1, 2, 4-triazolopyrimidines and their evaluation as antimicrobial agents

Abu-Hashem, Ameen A.,Hussein, Hoda A. R.,Abu-zied, Khadeja M.

, p. 120 - 130 (2017)

Abstract: 7-aminopyrimidin-5(1H)-one (5) was utilized as a starting material for the preparation of new, Schiff bases (13–19), amides 23, 24, imide 25, as well as thiourea derivatives 30–33 incorporating the triazolopyrimidines nucleus in their molecules. Structural elucidations for the new compounds were based upon compatible microanalytical and spectroscopic measurement. Biological evaluation indicated that compounds 23, 31, 33, 32, and 30 possess promising antimicrobial activities. Graphical Abstract: [InlineMediaObject not available: see fulltext.]

NEW PYRIMIDINE DERIVATIVES FOR PREVENTION AND TREATMENT OF GRAM-NEGATIVE BACTERIAL INFECTION, CONTAMINATION AND FOULING

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Page/Page column 110, (2020/10/28)

New pyrimidine derivatives together with a membrane penetrating agent, optionally with a detectable isotope and pharmaceutical composition for use in treatment or prevention of Gram-negative bacterial infection in a host mammal in need of such treatment or prevention and use as inhibitors of Gram-negative biofilm formation on a surface of biomaterial or medical device, particularly of cardiovascular device such as prosthetic heart valve or pacemakers. New pyrimidine derivatives together with a membrane penetrating agent; for use as radiotracer in diagnosing or prognosing Gram-negative bacterial infection in a host mammal.

PYRIMIDINE DERIVATIVES FOR PREVENTION AND TREATMENT OF BACTERIAL INFECTIONS

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Page/Page column 98, (2019/09/04)

New pyrimidine derivatives of formula (I), optionally with a detectable isotope, pharmaceutical composition and method of preparation thereof. New pyrimidine derivatives for use in treatment or prevention of bacterial infection in a host mammal in need of such treatment or prevention and use as inhibitors of biofilm formation on a surface of biomaterial or medical device, particularly of cardiovascular device such as prosthetic heart valve or pacemakers. New pyrimidine derivatives for use as radiotracer in diagnosing or prognosing bacterial infection in a host mammal.

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