869209-22-3

Basic information

• Product Name: 1-bromo-4-((Z)-3-bromo-1-iodopropenyl)benzene
• Synonyms: 1-bromo-4-((Z)-3-bromo-1-iodopropenyl)benzene
• CAS NO: 869209-22-3
• Molecular Weight: 401.867
• Mol File: 869209-22-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-bromo-4-((Z)-3-bromo-1-iodopropenyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-bromo-4-((Z)-3-bromo-1-iodopropenyl)benzene(869209-22-3)
• EPA Substance Registry System: 1-bromo-4-((Z)-3-bromo-1-iodopropenyl)benzene(869209-22-3)

Safety Data

• Hazardous Substances Data: 869209-22-3(Hazardous Substances Data)

Upstream product

• 136350-66-8 1-bromo-4-(2,2-dibromovinyl)benzene 
• 1122-91-4 4-bromo-benzaldehyde 
• 452296-51-4 (Z)-3-(4-bromophenyl)-3-iodoprop-2-en-1-ol 
• 558-13-4 carbon tetrabromide 
• 37614-58-7 3-(4-bromophenyl)prop-2-yn-1-ol 
• 685139-28-0 (Z)-3-iodo-3-(4-(trifluoromethyl)phenyl)prop-2-en-1-ol 
• 343322-82-7 ethyl [(4-mercapto-2-methylphenyl)oxy]acetate 

Downstream Products

• 685139-18-8 Ethyl (Z)-[4-[3-(4-Bromophenyl)-3-iodoallylsulfanyl]-2-methylphenoxy]acetate 
• 869209-23-4 methyl (Z)-[4-[3-(4-bromophenyl)-3-iodoallyloxy]-2-methylphenoxy]acetate 
• 869209-24-5 (Z)-[4-[3-(4-bromophenyl)-5-phenylpent-2-en-4-ynyloxy]-2-methylphenoxy]acetic acid methyl ester 

Relevant articles and documents

E/Z Isomerization of 3,3-disubstituted allylic thioethers

Allylic thioethers of the general structure 1 underwent E/Z isomerization during both basic and acidic hydrolysis of the ester moiety at the remote end of the molecule. The isomerization was dependent on the substitution of the allylic moiety. The presenc

NOVEL COMPOUNDS, THEIR PREPARATION AND USE

Novel compounds of the general formula (I), in which the variables are as defined in claim 1, the use of these compounds as pharmaceutical compositions, pharmaceutical compositions comprising the compounds and methods of treatment employing these compound