476452-73-0

Basic information

• Product Name: methyl [(1-phenyl-1H-tetrazol-5-yl)sulfonyl]acetate
• Synonyms: methyl [(1-phenyl-1H-tetrazol-5-yl)sulfonyl]acetate
• CAS NO: 476452-73-0
• Molecular Weight: 282.28
• Mol File: 476452-73-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl [(1-phenyl-1H-tetrazol-5-yl)sulfonyl]acetate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl [(1-phenyl-1H-tetrazol-5-yl)sulfonyl]acetate(476452-73-0)
• EPA Substance Registry System: methyl [(1-phenyl-1H-tetrazol-5-yl)sulfonyl]acetate(476452-73-0)

Safety Data

• Hazardous Substances Data: 476452-73-0(Hazardous Substances Data)

Upstream product

• 86-93-1 1-Phenyl-1H-tetrazole-5-thiol 
• 3206-49-3 methyl (1-phenyltetrazol-5-ylthio)acetate 

Downstream Products

• 1264893-50-6 C₁₅H₁₈N₄O₅S 
• 868057-10-7 5-((S)-2-methylpentane-1-sulfonyl)-1-phenyl-1H-tetrazole 
• 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 
• 476452-74-1 (E)-(R)-3-Methyl-2-(1-phenyl-1H-tetrazole-5-sulfonyl)-hex-4-enoic acid methyl ester 
• 1448461-03-7 methyl (4E)-2-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]hex-4-enoate 
• 845734-51-2 5-{[(2S)-2-methylbut-3-en-1-yl]sulfonyl}-1-phenyl-1H-tetrazole 
• 1448461-05-9 methyl (4E)-5-phenyl-2-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]pent-4-enoate 
• 1448461-11-7 1-phenyl-5-{[(2R)-2-phenylbut-3-en-1-yl]sulfonyl}-1H-tetrazole 
• 1448461-04-8 methyl (4E)-2-[(1-phenyl-1H-tetrazol-5-yl)sulfonyl]hept-4-enoate 
• 1448461-10-6 5-{[(2S)-2-ethylbut-3-en-1-yl]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