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61937-71-1

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61937-71-1 Usage

General Description

2-Amino-5-bromo-4-pyrimidinol is a chemical compound that belongs to the class of pyrimidines. It is an intermediate used in the synthesis of pharmaceuticals and agrochemicals. It is also used in the production of UV stabilizers, antioxidants, and other organic compounds. 2-Amino-5-bromo-4-pyrimidinol has potential applications in the fields of medicine, agriculture, and materials science. It is an important building block for the synthesis of various biologically active molecules and functional materials.

Check Digit Verification of cas no

The CAS Registry Mumber 61937-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,3 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61937-71:
(7*6)+(6*1)+(5*9)+(4*3)+(3*7)+(2*7)+(1*1)=141
141 % 10 = 1
So 61937-71-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H4BrN3O/c5-2-1-7-4(6)8-3(2)9/h1H,(H3,6,7,8,9)

61937-71-1SDS

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-Amino-5-Bromo-4-Pyrimidinol

1.2 Other means of identification

Product number -
Other names 2-amino-5-bromo-1H-pyrimidin-6-one

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:61937-71-1 SDS

61937-71-1Upstream product

61937-71-1Relevant articles and documents

Synthetic routes to a series of proximal and distal 2′-deoxy fleximers

Wauchope, Orrette R.,Velasquez, Melvin,Seley-Radtke, Katherine

, p. 3496 - 3504 (2013/01/15)

Two series of innovative 2-deoxy nucleoside analogues have been designed where the nucleobase has been split into its imidazole and pyrimidine subunits. This structural modification serves to introduce flexibility into the nucleobase scaffold while still

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