3206-49-3

Basic information

• Product Name: Acetic acid, [(1-phenyl-1H-tetrazol-5-yl)thio]-, methyl ester
• CAS NO: 3206-49-3
• Molecular Formula: C10H10N4O2S
• Molecular Weight: 250.281
• Mol File: 3206-49-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Acetic acid, [(1-phenyl-1H-tetrazol-5-yl)thio]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, [(1-phenyl-1H-tetrazol-5-yl)thio]-, methyl ester(3206-49-3)
• EPA Substance Registry System: Acetic acid, [(1-phenyl-1H-tetrazol-5-yl)thio]-, methyl ester(3206-49-3)

Safety Data

• Hazardous Substances Data: 3206-49-3(Hazardous Substances Data)

Upstream product

• 2365-48-2 Methyl thioglycolate 
• 86-93-1 1-Phenyl-1H-tetrazole-5-thiol 
• 96-32-2 bromoacetic acid methyl ester 
• 96-34-4 methyl chloroacetate 

Downstream Products

• 46505-33-3 [(1-phenyl-1H-tetrazol-5-yl)thio]acetic acid 
• 13980-80-8 (1-phenyl-1H-tetrazol-5-ylthiol)acetic acid hydrazide 
• 138841-20-0 (1-phenyltetrazol-5-ylthio)acetamide 
• 138841-23-3 (1-phenyltetrazol-5-ylthio)acetohydroxamic acid 
• 476452-73-0 methyl [(1-phenyl-1H-tetrazol-5-yl)sulfonyl]acetate 
• 138841-26-6 (1-phenyltetrazol-5-ylthio)acetylthiosemicarbazide 
• 138841-25-5 (1-phenyltetrazol-5-ylthio)acetylsemicarbazide 
• 133506-40-8 (1-phenyltetrazol-5-ylthio)acetyl chloride 
• 868057-10-7 5-((S)-2-methylpentane-1-sulfonyl)-1-phenyl-1H-tetrazole 
• 476452-74-1 (E)-(R)-3-Methyl-2-(1-phenyl-1H-tetrazole-5-sulfonyl)-hex-4-enoic acid methyl ester 
• 476452-87-6 5-{[(2R,3E)-2-methylpent-3-en-1-yl]sulfonyl}-1-phenyl-1H-tetrazole 
• 476452-75-2 5-{[(2R)-2-methylpentyl]sulfonyl}-1-phenyl-1H-tetrazole 

Relevant articles and documents

Practical synthesis of β-carbonyl phenyltetrazolesulfones and investigations of their reactivities in organocatalysis

A practical synthesis of β-carbonyl phenyltetrazolesulfones, useful for a series of enantioselective reactions, is shown. Aryl, alkyl and ester carbonyl compounds all proved to be efficiently synthesised, leading to products in up to >99% yield over two s

Ruthenium-catalyzed alkene-alkyne coupling: Synthesis of the proposed structure of amphidinolide A

The ruthenium-catalyzed alkene-alkyne coupling provides a powerful method for the synthesis of 1,4 dienes and a way to simplify synthetic strategy. The latter potential is explored in the context of a synthesis of the assigned structure of amphidinolide A