1104546-96-4

Basic information

• Product Name: 2-(2H-1,2,3-triazol-2-yl)-5-Methyl-benzoyl chloride
• Synonyms: 2-(2H-1,2,3-triazol-2-yl)-5-Methyl-benzoyl chloride;5-methyl-2-(2H-1,2,3-triazol-2-yl)benzoyl chloride
• CAS NO: 1104546-96-4
• Molecular Formula: C₁₀H₈ClN₃O
• Molecular Weight: 221.64302
• EINECS: -0
• Mol File: 1104546-96-4.mol
• Article Data: 26

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2H-1,2,3-triazol-2-yl)-5-Methyl-benzoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2H-1,2,3-triazol-2-yl)-5-Methyl-benzoyl chloride(1104546-96-4)
• EPA Substance Registry System: 2-(2H-1,2,3-triazol-2-yl)-5-Methyl-benzoyl chloride(1104546-96-4)

Safety Data

• Hazardous Substances Data: 1104546-96-4(Hazardous Substances Data)

Usage

General Description

2-(2H-1,2,3-triazol-2-yl)-5-Methyl-benzoyl chloride is a chemical compound with the molecular formula C9H7ClN4O. It is a benzoyl chloride derivative containing a 1,2,3-triazole ring and a methyl group. 2-(2H-1,2,3-triazol-2-yl)-5-Methyl-benzoyl chloride is widely used in organic synthesis, particularly in the formation of triazole-based compounds. It is known for its reactivity and ability to undergo various chemical reactions, making it an important building block in pharmaceutical and agrochemical research. Its unique structure and properties make it a valuable tool in the development of new compounds with potential biological activities.

Upstream product

• 52548-14-8 2-iodoyl-5-methylbenzoic acid 
• 956317-36-5 2-(2H-1,2,3-triazol-2-yl)-5-methylbenzoic acid 

Downstream Products

• 1088993-96-7 5-fluoro-2-(((3R,6R)-1-(2-iodo-5-methyl-benzoyl)-6-methyl-piperidin-3-yl)methoxy)pyridine 
• 1030377-33-3 Suvorexant 
• 1381970-69-9 N-ethyl-N-{2-[4-(5-fluoropyridin-2-yl)-1H-pyrazol-1-yl]ethyl}-5-methyl-2-(2H-1,2,3-triazol-2-yl)benzamide 
• 1410039-27-8 N-ethyl-N-{2-[5-(5-fluoropyridin-2-yl)-1,2,4-oxadiazol-3-yl]ethyl}-5-methyl-2-(2H-1,2,3-triazol-2-yl)benzamide 
• 1381972-02-6 N-ethyl-N-(2-hydroxyethyl)-5-methyl-2-(2H-1,2,3-triazol-2-yl)benzamide 
• 1222456-90-7 {(3R,6R)-6-methyl-1-[5-methyl-2-(2H-1,2,3-triazol-2-yl)benzoyl]piperidin-3-yl}methanol 
• 1030377-80-0 (S)-(4-(5-chlorobenzo[d]oxazol-2-yl)-7-methyl-1,4-diazepan-1-yl)(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone 

Relevant articles and documents

Palladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation of 1,4-Diazepan-5-ones

We report the palladium-catalyzed asymmetric allylic alkylation of 1,4-diazepan-5-ones. This reaction proceeds smoothly to give gem-disubstituted diazepanone heterocycles bearing various functional groups in up to >99% yield and up to 95% ee. An electron-

METHOD FOR PRODUCING (2S)-2-[(1H-PYRAZOL-1-YL)METHYL]-1,3-OXAZINANE DERIVATIVE

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Octahydropyrrolo[3,4-c]pyrrole derivative and application method and application thereof

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