1396745-74-6

Basic information

• Product Name: (S)-2,3-di[(E)-2-methyl-2-butenoyloxy]propyl n-hexadecanoate
• CAS NO: 1396745-74-6
• Molecular Weight: 494.712
• Mol File: 1396745-74-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2,3-di[(E)-2-methyl-2-butenoyloxy]propyl n-hexadecanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2,3-di[(E)-2-methyl-2-butenoyloxy]propyl n-hexadecanoate(1396745-74-6)
• EPA Substance Registry System: (S)-2,3-di[(E)-2-methyl-2-butenoyloxy]propyl n-hexadecanoate(1396745-74-6)

Safety Data

• Hazardous Substances Data: 1396745-74-6(Hazardous Substances Data)

Upstream product

• 112-67-4 n-hexadecanoyl chloride 
• 57416-03-2 (R)-2,2-dimethyl-1,3-dioxolan-4-ylmethyl n-hexadecanoate 
• 35660-94-7 (E)-2-methylbut-2-enoyl chloride 
• 19670-51-0 (R)-2,3-dihydroxypropyl n-hexadecanoate 

Relevant articles and documents

Pheromone synthesis. Part 253: Synthesis of the racemates and enantiomers of triglycerides of male Drosophila fruit flies with special emphasis on the preparation of enantiomerically pure 1-monoglycerides

The racemates and enantiomers of triglycerides 1aee (2,3-ditigloyloxypropyl esters of palmitic, palmitoleic, stearic, oleic, and linoleic acids) of male Drosophila fruit flies were synthesized in three steps from the racemate and enantiomers of 2,3-acetoneglycerol (2) via 1-monoglycerides 4aee derived from the above fatty acids. Appropriate conditions were established for the preparation of enantiomerically pure 1-monoglycerides 4aee, and their enantiomeric purities were determined by NMR analysis of the corresponding bis-(R)-MTPA esters.