144936-85-6

Basic information

• Product Name: (E)-6-{2-[2-(2,5-Diphenyl-oxazol-4-yl)-ethyl]-[1,3]dioxolan-2-yl}-hex-5-en-2-ol
• CAS NO: 144936-85-6
• Molecular Weight: 419.521
• Mol File: 144936-85-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-6-{2-[2-(2,5-Diphenyl-oxazol-4-yl)-ethyl]-[1,3]dioxolan-2-yl}-hex-5-en-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-6-{2-[2-(2,5-Diphenyl-oxazol-4-yl)-ethyl]-[1,3]dioxolan-2-yl}-hex-5-en-2-ol(144936-85-6)
• EPA Substance Registry System: (E)-6-{2-[2-(2,5-Diphenyl-oxazol-4-yl)-ethyl]-[1,3]dioxolan-2-yl}-hex-5-en-2-ol(144936-85-6)

Safety Data

• Hazardous Substances Data: 144936-85-6(Hazardous Substances Data)

Upstream product

• 2549-30-6 4-Methyl-2,5-diphenyloxazole N-oxide 
• 2549-33-9 4-(chloromethyl)-2,5-diphenyloxazole 
• 144762-97-0 4-(4-Triphenylphosphoranylidene-3-butanon)-2,5-diphenyloxazole 
• 144936-87-8 2-(2',2',2'-Trichloroethylcarbonoyl)-6-methyl-5-heptene 
• 144762-96-9 4-(2',2',2'-Trichloroethylcarbonoyl)pentanal 
• 4630-06-2 6-methylhept-5-en-2-ol 
• 107-21-1 ethylene glycol 
• 144936-88-9 4-<3-Oxo-8-(2',2',2'-trichloroethylcarbonoyl)-4-E-nonen>-2,5-diphenyloxazole 

Relevant articles and documents

The Singlet Oxygen Conversion of Oxazoles to Triamides. Application in the Synthesis of (+/-)-Pyrenolide C. Assignment of Stereochemistry.

Pyrenolide C has been synthesized for the first time using an oxazole template to construct the framework of the ten-membered unsaturated lactone system.The stereochemical assignment of the allylic alcohol substituent, based on the mode of synthesis, has