104047-01-0

Basic information

• Product Name: (3RS,4RS)-(E)-3-phenylhept-1,5-dien-4-ol
• CAS NO: 104047-01-0
• Molecular Weight: 188.269
• Mol File: 104047-01-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (3RS,4RS)-(E)-3-phenylhept-1,5-dien-4-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (3RS,4RS)-(E)-3-phenylhept-1,5-dien-4-ol(104047-01-0)
• EPA Substance Registry System: (3RS,4RS)-(E)-3-phenylhept-1,5-dien-4-ol(104047-01-0)

Safety Data

• Hazardous Substances Data: 104047-01-0(Hazardous Substances Data)

Upstream product

• 21087-29-6 trans-3-phenylprop-2-enyl chloride 
• 123-73-9 crotonaldehyde 
• 673-32-5 1-Phenylprop-1-yne 
• 6117-91-5 (E/Z)-2-buten-1-ol 
• 21040-45-9 Cinnamyl acetate 
• 103-54-8 cinnamyl acetate 
• 123-73-9 trans-Crotonaldehyde 

Relevant articles and documents

Iridium-catalyzed coupling reaction of primary alcohols with 1-aryl-1-propynes leading to secondary homoallylic alcohols

We report iridium-catalyzed coupling of 2-alkynes such as 1-aryl-1-propynes with primary alcohols leading to secondary homoallylic alcohols as products. This reaction involves an iridium-catalyzed novel catalytic transformation of 2-alkynes and primary al

DIASTEREOSELECTIVITY, DIASTEREOFACIAL SELECTIVITY AND REGIOSELECTIVITY IN THE REACTIONS OF CYNNAMYL CHLORIDE WITH ALDEHYDES MEDIATED BY TIN AND ALUMINIUM

The reaction of cinnamyl chlorie with a series of aryl and alkyl aldehydes mediated by tin and aluminium has been shown to be regioselective and threo diastereoselective.For aldehydes with chirality adjacent to the carbonyl function some diastereofacial s

REDUCTIVE GENERATION OF ACTIVE ZERO-VALENT TIN IN SnCl2-Al SYSTEM AND ITS USE FOR HIGHLY DIASTEREOSELECTIVE REACTION OF CINNAMYL CHLORIDE AND ALDEHYDES.

Highly diastereoselective reaction of cinnamyl chloride with aldehydes was achieved by the use of active zero-valent tin generated in SnCl2-Al system.