Welcome to LookChem.com Sign In|Join Free
  • or
3-(4-methylbenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-ol is a chemical compound belonging to the class of triazolotriazolopyrimidines. It is characterized by its unique molecular structure, which features a triazole and a pyrimidine ring fused together, with a methylbenzyl group attached to the 3-position. 3-(4-methylbenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-ol is of interest in the field of organic chemistry and pharmaceutical research due to its potential applications and properties.

258356-16-0

Post Buying Request

258356-16-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

258356-16-0 Usage

Uses

Used in Pharmaceutical Industry:
3-(4-methylbenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-ol is used as a reactant in the preparation of triazolotriazolopyrimidines. These compounds have shown potential as therapeutic agents, particularly in the development of novel drugs targeting various diseases and conditions. The unique structure of 3-(4-methylbenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-ol allows for further chemical modifications and functionalization, which can lead to the discovery of new bioactive molecules with improved pharmacological properties.
Used in Chemical Research:
In the field of chemical research, 3-(4-methylbenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-ol serves as a valuable starting material for the synthesis of more complex and diverse chemical structures. Its reactivity and functional groups make it an attractive candidate for various synthetic transformations, which can lead to the development of new compounds with potential applications in various industries, such as materials science, agrochemistry, and pharmaceuticals.
Used in Material Science:
The unique molecular structure of 3-(4-methylbenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-ol also makes it a candidate for potential applications in material science. Its properties, such as stability and the ability to form specific interactions with other molecules, could be exploited to develop new materials with tailored properties for various applications, including electronics, sensors, and advanced materials for energy storage and conversion.

Check Digit Verification of cas no

The CAS Registry Mumber 258356-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,8,3,5 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 258356-16:
(8*2)+(7*5)+(6*8)+(5*3)+(4*5)+(3*6)+(2*1)+(1*6)=160
160 % 10 = 0
So 258356-16-0 is a valid CAS Registry Number.

258356-16-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(4-methylphenyl)methyl]-2H-triazolo[4,5-d]pyrimidin-7-one

1.2 Other means of identification

Product number -
Other names 3-(4-methylbenzyl)-3,6-dihydro-7H-[1,2,3]triazolo[4,5-d]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:258356-16-0 SDS

258356-16-0Relevant academic research and scientific papers

1,2,3-Triazolo[4,5-e]-1,2,4-triazolo[3,4-c]pyrimidines

Biagi, Giuliana,Giorgi, Irene,Livi, Oreste,Manera, Clementina,Scartoni, Valerio

, p. 1195 - 1198 (2007/10/03)

Some new 1,2,3-triazolo[4,5-e]-1,2,4-triazolo[3,4-c]pyrimidines were prepared starting from the corresponding 1,2,3-triazolo[4,5-d]pyrimidines via the formation of the 1,2,4-triazole ring. Thus suitable hydrazino derivatives 6 were condensed with triethyl orthoformate, triethyl orthoacetate and triethyl orthobenzoate to give the expected tricyclic derivatives 7, 8 and 9. Intramolecular cyclization of the ethoxycarbonylhydrazino derivatives 10 gave the tricyclic compounds 11 bearing an hydroxyl group in the 3 position. The v-triazolo-s-triazolopyrimidine derivatives were tested towards the A1 and A(2A) adenosine receptors in binding assays, but they did not show any receptor affinity.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 258356-16-0