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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.

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  • 41996-97-8 Structure
  • Basic information

    1. Product Name: 1-(4-Bromo-butyl)-4-vinylbenzene
    2. Synonyms: 1-(4-Bromo-butyl)-4-vinylbenzene;1-(4-bromobutyl)-4-ethenylbenzene
    3. CAS NO:41996-97-8
    4. Molecular Formula: C12H15Br
    5. Molecular Weight: 239.1515
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 41996-97-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(4-Bromo-butyl)-4-vinylbenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-Bromo-butyl)-4-vinylbenzene(41996-97-8)
    11. EPA Substance Registry System: 1-(4-Bromo-butyl)-4-vinylbenzene(41996-97-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 41996-97-8(Hazardous Substances Data)

41996-97-8 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 this compound. Its unique properties and reactivity make it an interesting subject for scientific investigation and potential innovation in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 41996-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,9,9 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41996-97:
(7*4)+(6*1)+(5*9)+(4*9)+(3*6)+(2*9)+(1*7)=158
158 % 10 = 8
So 41996-97-8 is a valid CAS Registry Number.

41996-97-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-bromobutyl)-4-ethenylbenzene

1.2 Other means of identification

Product number -
Other names 4-bromobutylstyrene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:41996-97-8 SDS

41996-97-8Relevant articles and documents

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

Bertini, Vincenzo,Alfei, Silvana,Pocci, Marco,Lucchesini, Francesco,Picci, Nevio,Iemma, Francesca

, p. 11407 - 11414 (2004)

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.

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

Hario, Akira,Kitamura, Masahiro,Loykulnant, Surapich

, p. 4770 - 4775 (2007/10/03)

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

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

Seki, Atsushi,Ishiwata, Fusae,Takizawa, Youichi,Asami, Masatoshi

, p. 5001 - 5011 (2007/10/03)

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

Process for producing hydroxyalkyl (METH) acrylates

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Page column 5-6, (2008/06/13)

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.

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