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41266-80-2

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41266-80-2 Usage

Description

5,7-DIMETHYL-[1,2,4]TRIAZOLO[4,3-A]PYRIMIDINE-3-THIOL is a chemical compound characterized by the molecular formula C7H8N4S. It is a triazolopyrimidine derivative featuring two methyl groups at the 5th and 7th positions and a thiol group at the 3rd position. 5,7-DIMETHYL-[1,2,4]TRIAZOLO[4,3-A]PYRIMIDINE-3-THIOL holds potential for various applications, particularly in the pharmaceutical and agricultural sectors, due to its possible antimicrobial, antifungal, and herbicidal properties. Ongoing research is exploring its full spectrum of biological activities and potential uses.

Uses

Used in Pharmaceutical Industry:
5,7-DIMETHYL-[1,2,4]TRIAZOLO[4,3-A]PYRIMIDINE-3-THIOL is used as a potential active pharmaceutical ingredient for its antimicrobial properties, aiming to combat various bacterial infections. Its unique structure and thiol group may contribute to its effectiveness against a range of pathogens.
Used in Agricultural Industry:
In the agricultural sector, 5,7-DIMETHYL-[1,2,4]TRIAZOLO[4,3-A]PYRIMIDINE-3-THIOL is considered for use as an antifungal agent to protect crops from fungal diseases, thereby improving crop yield and quality. Its potential herbicidal properties also make it a candidate for developing new herbicides to control unwanted plant growth in agricultural settings.
The exact applications and biological activities of 5,7-DIMETHYL-[1,2,4]TRIAZOLO[4,3-A]PYRIMIDINE-3-THIOL are still under investigation, with ongoing research aimed at fully understanding its potential and optimizing its use in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 41266-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,6 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41266-80:
(7*4)+(6*1)+(5*2)+(4*6)+(3*6)+(2*8)+(1*0)=102
102 % 10 = 2
So 41266-80-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N4S/c1-4-3-5(2)11-6(8-4)9-10-7(11)12/h3H,1-2H3,(H,10,12)

41266-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-dimethyl-2H-[1,2,4]triazolo[4,3-a]pyrimidine-3-thione

1.2 Other means of identification

Product number -
Other names 3-Mercapto-5,7-dimethyl-s-triazolo<4,3-a>pyrimidin

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:41266-80-2 SDS

41266-80-2Relevant articles and documents

Utility of 2-hydrazino-4,6-dimethylpyridine in heterocyclic synthesis

Al-Ashmawy,Abd El-Samii,El Feky,Osman

, p. 110 - 114 (2007/10/03)

2-Hydrazino-4,6-dimethylpyrimidine (1) readily underwent ring closure with benzoyl chloride to give 5,7-dimethyl-3 phenyl- 1,2,4-triazolo[4,3-a]pyrimidine (4a). Either N-benzoyl derivative (2) or the hydrazone (3a) can be used for formation of compound 4a. Reaction of compound 1 with acetylacetone gave the pyrazole derivative (6) rather than 1,2,4-triazepine derivative (5). The pyrrole (9) was the sole product from cyclization of 1 with 2,5 hexanedione. Reaction of compound 1 with carbon disulphide or ethyl chloroformate gave 1,2,4-triazolo[4,3-a]pyrimidines (10 and 12). The reaction of thiosemicarbazides (13 a-c) with ethyl bromoacetate and DCCD was investigated.

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