167367-93-3

Basic information

• Product Name: (E)-1-<2'-(3-hydroxy-4,4-dimethylpent-1-enyl)phenyl>ethanone
• Synonyms: (E)-1-<2'-(3-hydroxy-4,4-dimethylpent-1-enyl)phenyl>ethanone
• CAS NO: 167367-93-3
• Molecular Weight: 232.323
• Mol File: 167367-93-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-1-<2'-(3-hydroxy-4,4-dimethylpent-1-enyl)phenyl>ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-<2'-(3-hydroxy-4,4-dimethylpent-1-enyl)phenyl>ethanone(167367-93-3)
• EPA Substance Registry System: (E)-1-<2'-(3-hydroxy-4,4-dimethylpent-1-enyl)phenyl>ethanone(167367-93-3)

Safety Data

• Hazardous Substances Data: 167367-93-3(Hazardous Substances Data)

Upstream product

• 167367-79-5 2-[(E)-3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pent-1-enyl]-benzaldehyde 
• 167367-66-0 (E)-1-bromo-2-(3'-hydroxy-4',4'-dimethylpent-1'-enyl)benzene 
• 6630-33-7 ortho-bromobenzaldehyde 
• 67962-20-3 (E)-1-bromo-2-(4',4'-dimethyl-3'-oxopent-1'-enyl)benzene 
• 814-16-4 diethyl (3,3-dimethyl-2-oxobutyl)phosphonate 
• 167367-91-1 (E)-1-<2'(3-tert-butyldimethylsiloxy-4,4-dimethylpent-1-enyl)phenyl>ethanone 

Downstream Products

• 167368-05-0 C₂₂H₂₈N₂O₃S 
• 167368-12-9 Benzoic acid (E)-1-tert-butyl-3-[2-(1-diazo-ethyl)-phenyl]-allyl ester 
• 167367-92-2 (E)-1-(2'-acetylphenyl)-4,4-dimethylpent-1-en-3-yl benzoate 

Relevant articles and documents

Asymmetric Induction in the Electrocyclisations of 1,3 Dipolar Intermediates: the 1.7 Cyclisation of Diene-conjugated Diazo-compounds to give 1H-2,3-Benzodiazepines

In the cyclisation of the diene-conjugated diazo compounds 4 to give the diastereomeric pair of 1H-2,3-benzodiazepines 7 and 8, alkyl and silyl ethers when present as the 'medium' sized group R3, showed the opposite effect in controlling face selectivity