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6-(2-Hydroxyethyl)-5-methyl[1,2,4]triazolo[1,5-a]pyrimidin-7(4H)-one is a synthetic chemical compound that falls under the triazolopyrimidines category. It has a molecular formula of C9H10N4O2 and a molecular weight of 206.204 g/mol. 6-(2-HYDROXYETHYL)-5-METHYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDIN-7(4H)-ONE is characterized by a pyrimidine ring fused with a triazole ring, with a methyl and hydroxyethyl group as substituents. Due to its synthetic nature, it is not found naturally and must be produced in a laboratory setting. Although there is limited information available on its specific properties, uses, or potential hazards, it is essential for individuals handling 6-(2-HYDROXYETHYL)-5-METHYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDIN-7(4H)-ONE to adhere to standard laboratory safety protocols to mitigate any risks.

62053-06-9

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62053-06-9 Usage

Uses

Currently, there is limited information available on the specific applications of 6-(2-Hydroxyethyl)-5-methyl[1,2,4]triazolo[1,5-a]pyrimidin-7(4H)-one. However, given its chemical structure and the fact that it is a synthetic compound, it is likely that it could be used in various industries, such as pharmaceuticals, materials science, or chemical research, for different purposes. Some potential uses could include:
Used in Pharmaceutical Industry:
6-(2-Hydroxyethyl)-5-methyl[1,2,4]triazolo[1,5-a]pyrimidin-7(4H)-one could be used as a building block or intermediate in the synthesis of pharmaceutical compounds, given its unique structure and functional groups.
Used in Materials Science:
6-(2-HYDROXYETHYL)-5-METHYL[1,2,4]TRIAZOLO[1,5-A]PYRIMIDIN-7(4H)-ONE might be employed as a component in the development of new materials with specific properties, such as improved stability or reactivity, due to its triazolopyrimidine structure.
Used in Chemical Research:
6-(2-Hydroxyethyl)-5-methyl[1,2,4]triazolo[1,5-a]pyrimidin-7(4H)-one could serve as a subject of study in chemical research, where its properties, reactivity, and potential applications are further explored and understood.

Check Digit Verification of cas no

The CAS Registry Mumber 62053-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,5 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62053-06:
(7*6)+(6*2)+(5*0)+(4*5)+(3*3)+(2*0)+(1*6)=89
89 % 10 = 9
So 62053-06-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N4O2/c1-5-6(2-3-13)7(14)12-8(11-5)9-4-10-12/h4,13H,2-3H2,1H3,(H,9,10,11)

62053-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(2-hydroxyethyl)-5-methyl-1H-[1,2,4]triazolo[1,5-a]pyrimidin-7-one

1.2 Other means of identification

Product number -
Other names 6-(2-hydroxyethyl)-5-methyl-4,8-dihydro-1,2,4-triazolo[1,5-a]pyrimidin-7-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:62053-06-9 SDS

62053-06-9Downstream Products

62053-06-9Relevant academic research and scientific papers

PYRROLO [3, 2 -E] [1,2,4] TRIAZOLO [1,5 -A] PYRIMIDINES DERIVATIVES AS INHIBITORS OF MICROGLIA ACTIVATION

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Page/Page column 7-8, (2011/04/26)

The invention relates to novel compounds useful in the treatment and prophylaxis of disease. Compounds of the formula (I) wherein X is halogen, independently selected form chlorine and fluorine and n is 0, 1 or 2. and their pharmaceutically acceptable salts are useful in the treatment and prophylaxis of diseases caused by activation of microglia, particularly Alzheimer's disease.

PYRROLO [3,2 -E] [1,2,4] TRIAZOLO [1,5-A] PYRIMIDINES DERIVATIVES AS INHIBITORS OF MICROGLIA ACTIVATION

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Page/Page column 5, (2011/04/26)

The invention relates to novel compounds useful in the treatment and prophylaxis of disease. Compounds of the formula (I), wherein X is halogen, independently selected form chlorine and fluorine and their pharmaceutically acceptable salts are useful in th

Studies on Cardiovascular Agents. 6. Synthesis and Coronary Vasodilating and Antihypertensive Activities of 1,2,4-Triazolopyrimidines Fused to Heterocyclic Systems

Sato, Yasunobu,Shimoji, Yasuo,Fujita, Hiroshi,Nishino, Hiroshi,Mizuno, Hiroshi,et al.

, p. 927 - 937 (2007/10/02)

The synthesis and coronary vasodilating and antihypertensive activities of 1,2,4-triazolopyrimidines fused to pyrrole, thiophene, pyran, pyridine, and pyridazine are described.Among these compounds, 8-tert-butyl-7,8-dihydro-5-methyl-6H-pyrrolo3,2-

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