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7-Methyl-1,2,4-triazolo[4,3-a]pyridine, also known as MTR, is a heterocyclic chemical compound with the molecular formula C6H6N4. It features a pyridine ring fused with a triazolopyridine ring, making it a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and various substituted derivatives. MTR demonstrates potential antifungal and herbicidal activities, contributing to the development of new drugs and agricultural products. Additionally, it is utilized in the manufacturing of dyes, pigments, and other organic compounds, showcasing its importance in the fields of medicine, agriculture, and chemical industries.

4919-10-2

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4919-10-2 Usage

Uses

Used in Pharmaceutical Industry:
7-Methyl-1,2,4-triazolo[4,3-a]pyridine is used as a building block for the synthesis of pharmaceuticals due to its potential antifungal and herbicidal activities. It contributes to the development of new drugs by providing a structural foundation for the creation of various substituted derivatives.
Used in Agrochemical Industry:
In the agrochemical industry, 7-Methyl-1,2,4-triazolo[4,3-a]pyridine is utilized as a component in the development of new agricultural products. Its antifungal and herbicidal properties make it a valuable asset in creating effective solutions for crop protection and management.
Used in Chemical Industry:
7-Methyl-1,2,4-triazolo[4,3-a]pyridine is used in the manufacturing of dyes, pigments, and other organic compounds in the chemical industry. Its versatile chemical structure allows for the production of a wide range of colorants and specialty chemicals for various applications.
Used in Research and Development:
MTR serves as a valuable compound in research and development for the exploration of new chemical reactions, synthesis methods, and potential applications in various industries. Its unique structure and properties make it an interesting subject for scientific investigation and innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 4919-10-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,1 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4919-10:
(6*4)+(5*9)+(4*1)+(3*9)+(2*1)+(1*0)=102
102 % 10 = 2
So 4919-10-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3/c1-6-2-3-10-5-8-9-7(10)4-6/h2-5H,1H3

4919-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methyl-[1,2,4]triazolo[4,3-a]pyridine

1.2 Other means of identification

Product number -
Other names 7-Methyl-s-triazolo<4,3-a>pyridin

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:4919-10-2 SDS

4919-10-2Downstream Products

4919-10-2Relevant academic research and scientific papers

Metal free [4+1] and [5+1] annulation reactions to prepare heterocycles using DMF and its derivatives as one-carbon source

Liu, Lingfeng,Qiao, Chunhua,Shen, Bei,Xu, Yiwen

, (2020/04/01)

1,2,4-Triazolo[3,4-a]pyridines and related heterocycles and substituted triazines were commonly discovered scaffolds in a variety of pharmaceutical and agrochemical agents. Herein, we report a highly efficient and practical method using DMF and its derivative for the [4+1] and [5+1] annulation reactions to prepare these heterocycles. This metal free reaction takes advantages of shelf stable DMF as solvent and carbon donor, imidazole chloride as a catalyst, the mild reaction condition tolerates a broad substrate range and substitutes. The prepared 3-unsubstituted 1,2,4-triazolo[3,4-a]pyridine and derivatives allow further introduction of a variety of functional group1 at 3-position.

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