127516-27-2

Basic information

• Product Name: (2R,5E,9E)-2,6,10-trimethylundeca-5,9-dien-1-ol
• CAS NO: 127516-27-2
• Molecular Weight: 210.36
• Mol File: 127516-27-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2R,5E,9E)-2,6,10-trimethylundeca-5,9-dien-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,5E,9E)-2,6,10-trimethylundeca-5,9-dien-1-ol(127516-27-2)
• EPA Substance Registry System: (2R,5E,9E)-2,6,10-trimethylundeca-5,9-dien-1-ol(127516-27-2)

Safety Data

• Hazardous Substances Data: 127516-27-2(Hazardous Substances Data)

Upstream product

• 108-05-4 vinyl acetate 
• 24120-53-4 2,6-Dimethyl-2,6-undecadiene-10-ene 
• 75-24-1 trimethylaluminum 
• 127483-90-3 2-((E)-(R)-2,6,10-Trimethyl-4-phenylsulfanyl-undeca-5,9-dienyloxy)-tetrahydro-pyran 
• 22339-13-5 (E)-9-iodo-2,6-dimethylnona-2,6-diene 
• 198268-26-7 (2R,5E,9E)-N-[(1S,2S)-2-hydroxy-1-methyl-2-phenylethyl]-2,6,10,N-tetramethylundeca-5,9-dienamide 
• 128419-46-5 2-((E)-(R)-2,6,10-Trimethyl-undeca-5,9-dienyloxy)-tetrahydro-pyran 

Downstream Products

• 24048-13-3 (R,E)-2,6,10-trimethylundeca-5,9-dienal 

Relevant articles and documents

Zirconium-catalyzed asymmetric carboalumination of alkenes: ZACA-lipase-catalyzed acetylation synergy

ZACA-lipase-catalyzed acetylation tandem reactions provide highly efficient and selective routes to either (R)- or (S)-2-methyl-1-alkanols, making, for the first time, the ZACA-based asymmetric synthesis of 2-methyl-1-alkanols widely applicable and satisfactory.

THE TOTAL SYNTHESIS OF 10-(R,S)-C30 BOTRYOCOCCENE AND BOTRYOCOCCANE AND A NEW SYNTHESIS OF A GENERAL INTERMEDIATE TO THE BOTRYOCOCCENE FAMILY.

The first synthesis of a C-30 botryococcene has been achieved by using a modified Julia reaction for the key coupling of fragments (2) and (3).The same strategy has been used in a new synthesis of a known synthetic precursor to the entire botryococcene family.