CAS: 1592-20-7
Pureté: 99%
Molecular Formula: C9H9Cl
Molecular Weight: 152.62
EINECS: 216-471-2
Storace Perod: Normal temperature storage
Synonyms: 1-(chloromethyl)-4-ethenyl-benzen; 1-(chloromethyl)-4-ethenyl-Benzene; 4-(CHLOROMETHYL)STYRENE; 4-VINYLBENZYLCHLORIDE; 1-(chloromethyl)-4-vinylbenzene; 4-VINYLBENZYLCHLORIDE,STAB.; 4-Vinylbenylchloride; 4-Vinylbenzylchloride
4-Vinylbenzyl chloride CAS 1592-20-7 is a bifunctional monomer with high reactivity. By homopolymerization or copolymerization with other monomers, 4-Vinylbenzyl chloride can form high reactive chloromethyl polymer compounds, which can further occur a variety of organic reactions, introduce a variety of functional groups in the macromolecular chain, and obtain a variety of functional polymers. In addition, 4-Vinylbenzyl chloride has many applications in organic synthesis. Therefore, 4-Vinylbenzyl chloride is a monomer with a wide range of uses.
| CHLOROMETHYL STYRENE | ≥98% |
| SINGLE BROMINE COMPOUND | ≤1% |
| OTHER SINGLE IMPURITY | ≤2% |
| ISOMER RATIO |
ORTHO：1
PARA： 99 |
| INHIBITOR | 500PPM |
4-Vinylbenzyl chloride is a component of ion exchange resins, photoresist polymers, crosslinked fibers, coupling agents and conductive polymers. The starting material for preparing various copolymers. 1,2,3 bifunctional monomers. Easy to be substituted by chlorine to form derivatives.
4-Vinylbenzyl chloride is a widely used chemical intermediate, which has two reactive points, namely double bond and benzyl chloromethyl. A series of polymers can be synthesized by homopolymerization or copolymerization with other monomers. On this basis, functional polymers can be formed by benzyl nucleophilic substitution reaction. If the double bond is retained, the nucleophilic substitution of benzyl chloromethyl directly occurs, which can be used to synthesize herbicides and new high-efficiency flame retardants
25kg/tambour
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