76338-37-9

Basic information

• Product Name: 1,8-diacetoxy-trans-p-menth-2-ene
• CAS NO: 76338-37-9
• Molecular Weight: 254.326
• Mol File: 76338-37-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,8-diacetoxy-trans-p-menth-2-ene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,8-diacetoxy-trans-p-menth-2-ene(76338-37-9)
• EPA Substance Registry System: 1,8-diacetoxy-trans-p-menth-2-ene(76338-37-9)

Safety Data

• Hazardous Substances Data: 76338-37-9(Hazardous Substances Data)

Upstream product

• 15910-72-2 trans-p-menth-2-ene-1,8-diol 
• 616-38-6 carbonic acid dimethyl ester 
• 76338-36-8 1α-acetoxy-trans-p-menth-2-en-8-ol 
• 54145-81-2 1,2-epoxy-8-hydroxy-p-menthane 
• 76338-34-6 1α-hydroxy-2β-phenylseleno-trans-p-menthan-8-ol 
• 76358-34-4 Trifluoro-acetic acid 1-((1R,3R,4S)-4-acetoxy-4-methyl-3-phenylselanyl-cyclohexyl)-1-methyl-ethyl ester 
• 76338-33-5 1α-acetoxy-2α-phenylseleno-trans-p-menthan-8-ol 
• 76338-31-3 6-acetoxy-2-hydroxy-2,6-dimethyl-3-phenylseleno-octa-7-ene 
• 98-55-5 terpineol 
• 115-95-7 linalool acetate 
• 41610-76-8 1-(3,4-epoxy-4-methylpentyl)-1-methylallyl acetate 

Relevant articles and documents

Stereoselective Cyclization assisted by the Selenyl Group. Biogenetic-type Synthesis in the p-Menthane Series

Acid-catalysed cyclization of the β-hydroxyselenide (3), derived from linalyl acetate (1), afforded the trans-p-menthanes (4) and (5), the structures of which were confirmed by their transformation into (6), (11), (8), and (13), and alternative syntheses of these compounds.The structure determination of some products obtained by the reaction of limonene and α-terpineol epoxides with phenylselenium anion was also carried out.