41996-97-8

Basic information

• Product Name: 1-(4-Bromo-butyl)-4-vinylbenzene
• Synonyms: 1-(4-Bromo-butyl)-4-vinylbenzene;1-(4-bromobutyl)-4-ethenylbenzene
• CAS NO: 41996-97-8
• Molecular Formula: C₁₂H₁₅Br
• Molecular Weight: 239.1515
• Mol File: 41996-97-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(4-Bromo-butyl)-4-vinylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-Bromo-butyl)-4-vinylbenzene(41996-97-8)
• EPA Substance Registry System: 1-(4-Bromo-butyl)-4-vinylbenzene(41996-97-8)

Safety Data

• Hazardous Substances Data: 41996-97-8(Hazardous Substances Data)

Usage

General Description

1-(4-Bromo-butyl)-4-vinylbenzene, also known as 1-(4-Bromobutyl)-4-vinylbenzene, is a chemical compound with the molecular formula C14H17Br. It is a colorless to pale yellow liquid that is primarily used as a monomer in the production of plastics and polymers. It is also used as a reagent in organic synthesis, particularly in the production of specialty chemicals. 1-(4-Bromo-butyl)-4-vinylbenzene is classified as a flammable liquid and may pose health hazards if not handled and stored properly. It is important to use proper safety precautions when handling 1-(4-Bromo-butyl)-4-vinylbenzene to avoid potential risks.

Upstream product

• 1592-20-7 4-Vinylbenzyl chloride 
• 109-64-8 1,3-dibromo-propane 
• 110-52-1 1,4-dibromo-butane 
• 7459-73-6 (4-Vinylphenyl)magnesium chloride 

Downstream Products

• 820973-54-4 N-[4-(4-vinylphenyl)butyl]phthalimide 
• 725253-99-6 2-(4-(4-vinylphenyl)butoxy)acetophenone 
• 868162-40-7 5-(4-(4-ethenylphenyl)butoxy)methyl-1,3-dithiane 
• 725254-00-2 4-(4-(2-isopropenylphenoxy)butyl)styrene 
• 725254-01-3 4-(4-(4-isopropenylphenoxy)butyl)styrene 
• 725254-02-4 4-(4-(3-isopropenylphenoxy)butyl)styrene 
• 1013121-88-4 C₃₆H₄₆N₂O₆ 

Relevant articles and documents

Monomers containing substrate or inhibitor residues for copper amine oxidases and their hydrophilic beaded resins designed for enzyme interaction studies

Five styrenic monomers, four with aminoalkyl residues typical of copper containing amine oxidase substrates and one with a 2,6-dialkoxybenzylamine residue which mimics previously prepared selective substrate-like benzylamine oxidase inhibitors, have been synthesized and transformed into radical homopolymers, copolymers with N,N-dimethylacrylamide (DMAA), and hydrophilic beaded resins, designed for enzyme interaction studies aimed in finding new materials for highly biospecific chromatographic separations. The five monomers have given beaded resins of 125-500 μm swellable in water with a volume increase of 1200-1500%. The four aminoalkyl monomers have given water soluble copolymers some of which are good substrates of benzylamine oxidase (BAO), diamine oxidase (DAO) and lysyl oxidase (LO), up to 9.7 times better than elastin for LO. Graphical Abstract.

Crossed aldol reaction using cross-linked polymer-bound lithium dialkylamide

Cross-linked polymer-bound lithium dialkylamides were employed in crossed aldol reaction of various carbonyl compounds with aldehydes to afford the corresponding β-hydroxycarbonyl compounds. The introduction of spacer chains to the polymer-bound lithium d