123499-01-4

Basic information

• Product Name: (5E)-[1,1,1,3,3-²H₅]-6,10-dimethyl-undeca-5,9-dien-2-one
• Synonyms: (5E)-[1,1,1,3,3-²H₅]-6,10-dimethyl-undeca-5,9-dien-2-one
• CAS NO: 123499-01-4
• Molecular Weight: 199.277
• Mol File: 123499-01-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (5E)-[1,1,1,3,3-²H₅]-6,10-dimethyl-undeca-5,9-dien-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (5E)-[1,1,1,3,3-²H₅]-6,10-dimethyl-undeca-5,9-dien-2-one(123499-01-4)
• EPA Substance Registry System: (5E)-[1,1,1,3,3-²H₅]-6,10-dimethyl-undeca-5,9-dien-2-one(123499-01-4)

Safety Data

• Hazardous Substances Data: 123499-01-4(Hazardous Substances Data)

Upstream product

• 123499-00-3 <²H6>propan-2-one dimethylhydrazone 
• 5389-87-7 1-chloro-3,7-dimethylocta-2,6-diene 

Downstream Products

• 140231-44-3 (2RS,5E)-6,10-dimethyl-2-phenyl(1,1,1,3,3-2H₅)undeca-5,9-dien-2-ol 

Relevant articles and documents

Biosynthesis of Homoterpenes in Higher Plants

In higher plants, the two homoterpenes 4,8-dimethylnona-1,3,7-triene (1) and 4,8,12-trimethyldeca-1,3,7,11-tetraene (2) are synthesized from the regular terpene alcohols nerolidol and geranyllinalool by fragmentation into the homoterpene and butenone.The biosynthetic pathway is evidenced by conversion of (2H)nerolidol in Hoya purpureo-fusca, Magnolia liliiflora nigra, Robina pseudoacacia, and Philadelphus coronarius.