1338922-80-7

Basic information

• Product Name: (S)-1-(3,4-dichlorophenyl)-1-phenylbut-3-en-1-ol
• Synonyms: (S)-1-(3,4-dichlorophenyl)-1-phenylbut-3-en-1-ol
• CAS NO: 1338922-80-7
• Molecular Weight: 293.193
• Mol File: 1338922-80-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-1-(3,4-dichlorophenyl)-1-phenylbut-3-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-(3,4-dichlorophenyl)-1-phenylbut-3-en-1-ol(1338922-80-7)
• EPA Substance Registry System: (S)-1-(3,4-dichlorophenyl)-1-phenylbut-3-en-1-ol(1338922-80-7)

Safety Data

• Hazardous Substances Data: 1338922-80-7(Hazardous Substances Data)

Upstream product

• 401797-02-2 2-(3,4-dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 151169-75-4 3,4-dichlophenylboronic acid 
• 100-52-7 benzaldehyde 
• 77118-87-7 (S)-1-Phenyl-3-buten-1-ol 
• 80735-94-0 1-Phenyl-3-buten-1-ol 
• 1338922-77-2 (R)-2-(1-(3,4-dichlorophenyl)-1-phenylbut-3-enyl)-4,4,5,5-tetramethyl-[1,3,2]-dioxaborolane 
• 1063723-88-5 (S)-N,N-diisopropylcarbamic acid 1-phenyl-but-3-enyl ester 

Relevant articles and documents

Enantioselective syntheses of (+)-sertraline and (+)-indatraline using lithiation/borylation-protodeboronation methodology

The lithiation/borylation-protodeboronation of a homoallyl carbamate was applied to the synthesis of (+)-sertraline and (+)-indatraline. Due to the presence of the alkene, significant modifications of the methodology were required (use of 12-crown-4, TMSCl, H2O), or a solvent switch to CHCl3, to achieve high yields and high selectivities.