119815-08-6

Basic information

• Product Name: 5-[(2-furanylmethyl)thio]-1-phenyl-1H-tetrazole
• Synonyms: 5-[(2-furanylmethyl)thio]-1-phenyl-1H-tetrazole
• CAS NO: 119815-08-6
• Molecular Weight: 258.304
• Mol File: 119815-08-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 5-[(2-furanylmethyl)thio]-1-phenyl-1H-tetrazole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-[(2-furanylmethyl)thio]-1-phenyl-1H-tetrazole(119815-08-6)
• EPA Substance Registry System: 5-[(2-furanylmethyl)thio]-1-phenyl-1H-tetrazole(119815-08-6)

Safety Data

• Hazardous Substances Data: 119815-08-6(Hazardous Substances Data)

Upstream product

• 623-17-6 furfurylacetate 
• 86-93-1 1-Phenyl-1H-tetrazole-5-thiol 
• 98-00-0 (2-furyl)methyl alcohol 
• 18708-18-4 furfural tosylhydrazone 
• 98-01-1 furfural 
• 32276-00-9 S,S-bis(1-phenyl-1H-tetrazol-5-yl) dithiocarbonate 

Downstream Products

• 24954-15-2 phenacyl-2 furanne 

Relevant articles and documents

Direct Synthesis of Thioethers from Carboxylates and Thiols Catalyzed by FeCl3

A new and efficient method has been developed for the synthesis of thioethers from carboxylates and thiols. The reaction proceeds via a Fe(III)-catalyzed direct displacement of carboxylates from benzylic or allylic esters by heterocyclic thiols. Short rea

A straightforward synthesis of alkyl 1H-tetrazol-5-yl thioethers via a one-pot reaction of aldehydes and 1H-tetrazole-5-thiols mediated by N-tosylhydrazones

A straightforward approach for the synthesis of alkyl 1H-tetrazol-5-yl thioethers from aldehydes and 1H-tetrazole-5-thiol through a one-pot procedure is presented. The aldehydes were first condensed with N-tosylhydrazine to generate the N-tosylhydrazones,

Convenient synthesis of allylic sulfides and application to allylic carbon-carbon bond formation

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