404367-07-3

Basic information

• Product Name: (E)-ethyl 3-[(1R,2S,4S)-2-acetoxy-4-methyl-1-cyclohexyl]but-2-enoate
• Synonyms: (E)-ethyl 3-[(1R,2S,4S)-2-acetoxy-4-methyl-1-cyclohexyl]but-2-enoate
• CAS NO: 404367-07-3
• Molecular Weight: 268.353
• Mol File: 404367-07-3.mol

Chemical Properties

• CAS DataBase Reference: (E)-ethyl 3-[(1R,2S,4S)-2-acetoxy-4-methyl-1-cyclohexyl]but-2-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-ethyl 3-[(1R,2S,4S)-2-acetoxy-4-methyl-1-cyclohexyl]but-2-enoate(404367-07-3)
• EPA Substance Registry System: (E)-ethyl 3-[(1R,2S,4S)-2-acetoxy-4-methyl-1-cyclohexyl]but-2-enoate(404367-07-3)

Safety Data

• Hazardous Substances Data: 404367-07-3(Hazardous Substances Data)

Upstream product

• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 

Downstream Products

• 1027322-27-5 (3S,6R)-6-[(S)-3-(tert-Butyl-dimethyl-silanyloxy)-1-methyl-propyl]-2-[1,3]dithian-2-ylidene-3-methyl-1-(2-methyl-allyl)-cyclohexanol 
• 404367-11-9 (2R,5S)-2-[(R)-3-(3-tert-butyldimethylsilyloxy)-1-methylpropyl]-5-methyl-6-(1,3-dithian-2-ylidene)cyclohexan-1-one 
• 404367-01-7 (2'R,5R,8S)-3,8-dimethyl-5-(1,5-dimethyl-3-phenylsulfonylhex-4-enyl)-1-methoxy-5,6,7,8-tetrahydronaphthalene 
• 404367-16-4 (1S,2S,5R)-2-[(R)-3-(3-tert-butyldimethylsilyloxy)-1-methylpropyl]-5-methylcyclohexan-1-ol 
• 404367-10-8 (1S,2S,5R)-2-[(R)-3-(3-tert-butyldimethylsilyloxy)-1-methylpropyl]-5-methylcyclohexan-1-one 
• 404367-09-5 (1S,2R,5S)-2-[(S)-3-hydroxy-1-methylpropyl]-5-methylcyclohexan-1-ol 
• 404367-08-4 (3S)-ethyl 3-[(1R,2S,4S)-2-acetoxy-4-methyl-1-cyclohexyl]butanoate 

Relevant articles and documents

Enantiospecific syntheses of pseudopterosin aglycones. Part 2. Synthesis of pseudopterosin K-L aglycone and pseudopterosin A-F aglycone via a B→BA→BAC annulation strategy

The enantiomeric aglycones of pseudopterosins K-L and A-F are synthesised from (-)- and (+)-isopulegol respectively. Key features are (a) the construction of the C3 stereogenic centre by a directed epoxidation-reduction sequence (K-L); (b) the creation of