78539-91-0

Basic information

• Product Name: 7-METHYL-1,2,3-TRIAZOLO(1,5-A)PYRIDINE
• Synonyms: 7-METHYL-1,2,3-TRIAZOLO(1,5-A)PYRIDINE
• CAS NO: 78539-91-0
• Molecular Formula: C₇H₇N₃
• Molecular Weight: 133.15
• Mol File: 78539-91-0.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Density: 1.24g/cm³
• Refractive Index: 1.658
• CAS DataBase Reference: 7-METHYL-1,2,3-TRIAZOLO(1,5-A)PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 7-METHYL-1,2,3-TRIAZOLO(1,5-A)PYRIDINE(78539-91-0)
• EPA Substance Registry System: 7-METHYL-1,2,3-TRIAZOLO(1,5-A)PYRIDINE(78539-91-0)

Safety Data

• Hazard Codes: Xi
• Statements: 5-36/37/38
• Safety Statements: 15-26-36
• Hazardous Substances Data: 78539-91-0(Hazardous Substances Data)

Usage

General Description

7-METHYL-1,2,3-TRIAZOLO(1,5-A)PYRIDINE is a chemical compound with the molecular formula C8H7N3. It is a heterocyclic compound that consists of a pyridine ring fused to a triazole ring. 7-METHYL-1,2,3-TRIAZOLO(1,5-A)PYRIDINE is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It is also used as an intermediate in the production of various organic compounds. Additionally, 7-METHYL-1,2,3-TRIAZOLO(1,5-A)PYRIDINE has potential biological activities and has been investigated for its potential use in medicinal chemistry. Due to its versatility and significance in organic synthesis, this compound is of interest to researchers in the fields of chemistry, pharmacology, and agrochemicals.

InChI:InChI=1/C7H7N3/c1-6-3-2-4-7-5-8-9-10(6)7/h2-5H,1H3

Upstream product

• 38112-50-4 [1-(6-Methyl-pyridin-2-yl)-meth-(Z)-ylidene]-hydrazine 
• 6627-60-7 2-aminomethyl-6-methylpyridine 
• 1122-72-1 6-methyl-2-pyridinecarboxaldehyde 
• 82315-67-1 C₁₄H₁₅N₃O₂S 

Downstream Products

• 82325-35-7 2-(6-formylpyridine-2-yl)-1-(p-methoxyphenyl)ethanol 
• 82315-70-6 2-(6-dibromomethylpyridin-2-yl)-1-(p-methoxyphenyl)ethanol 
• 60398-59-6 ((6-methylpyridin-2-yl)methyl)diphenylphosphine oxide 
• 152091-40-2 methyl (E)-3-<2-<6-<3-(3-butoxyphenyl)-3-oxopropenyl>pyridin-2-yl>-1-<oxy>ethyl>benzoate 
• 152091-36-6 (E)-methyl <1-<oxy>-2-<6-(3-oxoundec-1-enyl)pyridin-2-yl>ethyl>benzoate 
• 152091-35-5 3-[1-(tert-Butyl-dimethyl-silanyloxy)-2-(6-formyl-pyridin-2-yl)-ethyl]-benzoic acid methyl ester 
• 152091-33-3 methyl 3-(1-hydroxy-2-<1,2,3>triazolo<1,5-a>pyridin-7-ylethyl)benzoate 
• 152091-34-4 methyl 3-<2-(6-formylpyridin-2-yl)-1-hydroxyethyl>benzoate 
• 13287-64-4 acetic acid 6-methyl-pyridin-2-ylmethyl ester 
• 1122-71-0 2-(Hydroxymethyl)-6-methylpyridine 
• 1122-72-1 6-methyl-2-pyridinecarboxaldehyde 

Relevant articles and documents

Method for synthesizing [1,2,3]triazole[1,5-a]pyridines compound through non-catalyst N-N coupling reaction

The invention relates to a method for synthesizing [1,2,3]triazole[1,5-a]pyridines compound through non-catalyst N-N coupling reaction. The invention discloses an efficient method for synthesizing a product at one step without using a catalyst under a mild condition from a 2-pyridylamine compound and nitroso tert-butyl ester as a mild nitrogen atom source. The method is free from the catalyst, thereaction step is reduced, the condition is extremely mild, the efficiency is high, and the later modification can be performed on the biological active molecular, thereby facilitating the industrialproduction of [1,2,3]triazole[1,5-a]pyridines compound.

Ruthenium-NHC-Catalyzed asymmetric hydrogenation of indolizines: Access to indolizidine alkaloids

Crossing N-bridges! A ruthenium/N-heterocyclic carbene (NHC) complex serves as the catalyst for the high-yielding and completely regioselective and asymmetric hydrogenation of substituted indolizines and 1,2,3-triazolo-[1,5-a] pyridines. This method shoul

Triazolopyridines. Part 2. Preparation of 7-Substituted Triazolopyridines by Directed Lithiation

The lithiation reactions of 1,2,3-triazolopyridine (1) to give the 7-lithio-derivative (4; R = Li), and of its 7-methyl derivative (16) to give the 7-lithiomethyl compound, are described.These lithium derivatives react with electrophiles, notably a