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

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

Uses

Used in Plastics and Polymers Industry:
1-(4-Bromo-butyl)-4-vinylbenzene is used as a monomer for the production of plastics and polymers. Its unique chemical structure allows it to be copolymerized with other monomers, resulting in materials with improved properties such as strength, flexibility, and chemical resistance.
Used in Organic Synthesis:
1-(4-Bromo-butyl)-4-vinylbenzene is used as a reagent in organic synthesis, particularly in the production of specialty chemicals. Its bromine atom can be used for various chemical reactions, such as substitution, addition, and elimination reactions, making it a versatile building block for the synthesis of complex organic compounds.
Used in Research and Development:
1-(4-Bromo-butyl)-4-vinylbenzene is also used in research and development for the study of polymer chemistry, material science, and the development of new applications for 1-(4-Bromo-butyl)-4-vinylbenzene. Its unique properties and reactivity make it an interesting subject for scientific investigation and potential innovation in various fields.

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 
• 1013121-88-4 C₃₆H₄₆N₂O₆ 
• 725254-02-4 4-(4-(3-isopropenylphenoxy)butyl)styrene 
• 725254-01-3 4-(4-(4-isopropenylphenoxy)butyl)styrene 
• 725254-00-2 4-(4-(2-isopropenylphenoxy)butyl)styrene 
• 868162-40-7 5-(4-(4-ethenylphenyl)butoxy)methyl-1,3-dithiane 

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

Living Anionic Polymerization of 4-(4-(2-isopropenylphenoxy)butyl)styrene: A New Dual-Functionalized Styrene Derivative Having α-Methylstyrene Functionality

The anionic polymerization of a substituted styrene with α-methylstyryl moiety, 4-(4-(2-isopropenylphenoxy)butyl)styrene (1), was carried out in THF at -78 deg C with sec-BuLi as an initiator. In the anionic polymerization, only the styryl group of 1 can

Process for producing hydroxyalkyl (METH) acrylates

In a process for producing hydroxyalkyl (meth)acrylates by the reaction of (meth)acrylic acid with an alkylene oxide, a thermally and chemically stable anion exchange resin is used as a catalyst, which resin contains a repeating unit represented by the following formula (1) as a component: wherein A is a straight chain alkylene group having 3 to 8 carbon atoms, each of R1, R2, and R3is a hydrocarbon group or an alkanol group having 1 to 4 carbon atoms, which may be substituted with a hydroxyl group, X?is a counter ion coordinated with an ammonium group, where the substituent A with the ammonium group may be substituted at any position of a benzene ring, and the benzene ring may be substituted with an alkyl group or a halogen atom. The process can economically efficiently produce hydroxyalkyl (meth)acrylates without disadvantages such as deterioration in properties of a distillation residue.