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[1,2,4]TRIAZOLO[1,5-C]PYRIMIDIN-5-OL is a heterocyclic chemical compound characterized by a molecular formula of C6H6N4O. It features a triazole ring fused to a pyrimidine ring, with a hydroxyl group attached to the fifth carbon of the pyrimidine ring. [1,2,4]TRIAZOLO[1,5-C]PYRIMIDIN-5-OL is not naturally occurring but can be synthesized in the laboratory. Its unique structure and potential biological activities make it a promising candidate for pharmaceutical applications and a valuable research tool in chemical and biological studies.

76044-31-0

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76044-31-0 Usage

Uses

Used in Pharmaceutical Industry:
[1,2,4]TRIAZOLO[1,5-C]PYRIMIDIN-5-OL is used as a potential drug candidate for the development of new medications. Its unique structure and potential biological activities contribute to its potential as a therapeutic agent.
Used in Chemical and Biological Research:
[1,2,4]TRIAZOLO[1,5-C]PYRIMIDIN-5-OL is used as a research tool in chemical and biological studies. Its unique structure allows researchers to explore its properties and potential interactions with biological systems, contributing to the advancement of scientific knowledge in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 76044-31-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,4 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 76044-31:
(7*7)+(6*6)+(5*0)+(4*4)+(3*4)+(2*3)+(1*1)=120
120 % 10 = 0
So 76044-31-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H4N4O/c10-5-6-2-1-4-7-3-8-9(4)5/h1-3H,(H,6,10)

76044-31-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3H-[1,2,4]triazolo[1,5-c]pyrimidin-5-one

1.2 Other means of identification

Product number -
Other names 6H-[1,2,4]Triazolo[1,5-c]pyrimidin-5-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:76044-31-0 SDS

76044-31-0Relevant academic research and scientific papers

The first reliable, general synthesis of the 5-oxo derivatives of 5,6-dihydro-1,2,4-triazolo[4,3-c]-pyrimidine and the rates of isomerization of the [4,3-c] compounds into their [1,5-c] isomers

Nagamatsu, Tomohisa,Fujita, Takayuki

, p. 631 - 636 (2007/10/03)

This paper describes a reliable synthesis of the 5-oxo derivatives (8) of 5,6-dihydro-1,2,4-triazolo[4,3-c]pyrimidine, by the reaction of 2-oxo-1,2-dihydropyrimidin-4-ylhydrazines (7) with the appropriate triethyl orthoesters in trifluoroacetic acid below 30°C or by the oxidative cyclization of their aldehyde hydrazones (10) with 70% nitric acid in trifluoroacetic acid below 40°C, and the rates of isomerization of the [4,3-c] compounds (8) into the [1,5-c] isomers (9).

Bis-s-triazolopyrimidine and Some Simple Derivatives

Brown, Desmond J.,Shinozuka, Kazuo

, p. 1147 - 1152 (2007/10/02)

A general synthetic route to the new tricyclic system bis-s-triazolopyrimidine, is reported.Thus the parent heterocycle (11a) is prepared from the key bicyclic intermediate, s-triazolopyrimidin-5-ylamine (7a), through the correspondi

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