89229-67-4

Basic information

• Product Name: (2E,4E)-hepta-2,4-dien-1-yltriphenyl phosphonium bromide
• Synonyms: (2E,4E)-hepta-2,4-dien-1-yltriphenyl phosphonium bromide
• CAS NO: 89229-67-4
• Molecular Weight: 437.359
• Mol File: 89229-67-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2E,4E)-hepta-2,4-dien-1-yltriphenyl phosphonium bromide(CAS DataBase Reference)
• NIST Chemistry Reference: (2E,4E)-hepta-2,4-dien-1-yltriphenyl phosphonium bromide(89229-67-4)
• EPA Substance Registry System: (2E,4E)-hepta-2,4-dien-1-yltriphenyl phosphonium bromide(89229-67-4)

Safety Data

• Hazardous Substances Data: 89229-67-4(Hazardous Substances Data)

Upstream product

• 33467-79-7 (2E,4E)-hepta-2,4-dien-1-ol 
• 603-35-0 triphenylphosphine 
• 4313-03-5 (2E,4E)-hepta-2,4-dienal 

Downstream Products

• 84000-59-9 3-<(1E,3E,7E,9E)-1,3,5,7,9-dodecapentaenyloxy>-1,2-propanediol 

Relevant articles and documents

Total synthesis of amaminol A: Establishment of the absolute stereochemistry

The first synthetic route to amaminol A with use of an organocatalytic intramolecular Diels-Alder reaction is reported. The absolute stereochemistry is proven with a crystallographic image of a cyclic carbamate of amaminol A.

SYNTHESIS OF RACEMIC FECAPENTAENE-12, A POTENT MUTAGEN FROM HUMAN FECES, AND ITS REGIOISOMER

Racemic fecapentaene-12 and its regioisomer 2-(1,3,5,7,9-dodecapentaenyloxy)-1,3-propanediol (2) have been synthesized.The latter compound is comparably mutagenic to 1.