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Detail of > 1592-20-7

  • MSDS Download
  • CAS Number:
  • 1592-20-7
  • Name:
  • Benzene,1-(chloromethyl)-4-ethenyl-

  • Superlist Name:
  • 4-Vinylbenzyl chloride
  • Formula:
  • C9H9Cl
  • Molecular Structure:
  • Synonyms:
  • Styrene,p-(chloromethyl)- (6CI,7CI,8CI);1-(Chloromethyl)-4-vinylbenzene;4-(Chloromethyl)styrene;CMS 14;p-(Chloromethyl)styrene;p-Vinylbenzyl chloride;
  • Molecular Weight:
  • 152.62
  • EINECS:
  • 216-471-2
  • Density:
  • 1.066 g/cm3
  • Boiling Point:
  • 228.9 °C at 760 mmHg
  • Flash Point:
  • 90.4 °C
  • Appearance:
  • clear yellow liquid
  • Hazard Symbols:
  • CorrosiveC
  • Risk Codes:
  • 34-43-21/22
  • Safety:
  • 26-36/37/39-45Details
  • Transport Information:
  • UN 3265 8/PG 3
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CAS No. 

1592-20-7 4-Vinylbenzyl chlorideCompetitive Product

China (Mainland)   2404
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CAS No. 

1592-20-7 4-Vinylbenzyl chloride

China (Mainland)   QS  6760
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CAS No. 

1592-20-7 4-Vinylbenzyl chloride

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1592-20-7 4-Vinylbenzyl chloride

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1592-20-7 4-Vinylbenzyl chloride

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CAS No. 

1592-20-7 4-Vinylbenzyl chloride

Vinyl Benzene Chloride
China (Mainland)   490
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CAS No. 

1592-20-7 4-Vinylbenzyl chloride

4-Chloromethyl styrene Product Name: Chloromethyl styrene / 4-Chloromethyl styrene CAS:1592-20-7 Synonyms: Vinylbenzyl Chloride; VBC; CMS Structure: Index Name Index Appearance Light yellow to colorless liquid Assay(GC) 95% min Package: 200kg per plastic drum 60*90cm
China (Mainland)   4
  • Tel:86-22-84315261
  • Address:tianjin

CAS No. 

1592-20-7 4-Vinylbenzyl chloride

Chemical Name: 1-(Chloromethyl)-4-ethenylbenzene Molecular Formula: C9H9Cl Formula Weight: 152.62 CAS No.: 1592-20-7
China (Mainland)  
  • Tel:+86-578-2271396 86-578-2271365
  • Address:Xinyaocun, Qingyuan, Zhejiang, China

CAS No. 

1592-20-7 4-Vinylbenzyl chloride

VINYLBENZYL CHLORIDE
China (Mainland)  
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  • Address:Shiner Bldg,Jiaxing,314001,Zhejiang

CAS No. 

1592-20-7 4-Vinylbenzyl chloride

VINYLBENZYL CHLORIDE
China (Mainland)   6
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  • Address:Rm GB, No.2 Building Hai Fu Garden, No.1359, Dong Fang Road, Pu Dong New District, Shanghai 200127, P. R. China

CAS No. 

1592-20-7 4-Vinylbenzyl chloride

China (Mainland)   88
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CAS No. 

1592-20-7 4-Vinylbenzyl chloride

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    Reference

    Synthesis of polymeric formamides and their use as phase transfer catalysts
    Synthesis of polymeric formamides and their use as phase transfer catalysts. Kondo, Shuji; Inagaki, Yasuhito; Tsuda, Kazuichi (Nagoya Inst. Technol., Nagoya 466, Japan). J. Polym. Sci., Polym. Lett. Ed., 22(5), 249-54 (English) 1984. CODEN: JPYBAN. ISSN: 0360-6384. DOCUMENT TYPE: Journal CA Section: 35 (Chemistry of Synthetic High Polymers) Section cross-reference(s): 23, 25 N-Methylformamide [123-39-7] was treated with p-chloromethylstyrene [1592-20-7] to give N-methyl-N-(p-vinylbenzyl)formamide (I) [90499-42-6], which was homopolymd. and copolymd. with styrene (II) to give I polymers [90505-83-2] and I-II copolymer [90505-84-3], useful as phase-transfer catalysts for the reaction of alkyl bromides with nucleophiles. The catalytic activity of I-II copolymer increased with increasing II content. The reactivity ratios and Q-e values for the polymn. of II with I were given.
    Functional polymers and sequential copolymers by phase transfer catalysis
    Functional polymers and sequential copolymers by phase transfer catalysis. 12. Functional polymers containing 2-(p-phenoxy)-2-oxazoline pendant groups. Percec, V.; Nava, H.; Rodriguez-Parada, J. M. (Dep. Macromol. Sci., Case West. Reserve Univ., Cleveland, OH 44106, USA). Polym. Bull. (Berlin), 12(3), 261-8 (English) 1984. CODEN: POBUDR. ISSN: 0170-0839. DOCUMENT TYPE: Journal CA Section: 35 (Chemistry of Synthetic High Polymers) Two methods for prepg. functional polymers contg. 2-oxazoline pendant groups are presented. The 1st consists of the phase transfer-catalyzed etherification of 2-(p-hydroxyphenyl)-2-oxazoline (I) [81428-58-2] with m- [39833-65-3] and p-(chloromethyl)styrene [1592-20-7] to give m- [94099-19-1] and p-vinylbenzyl ethers [94060-31-8] of I. Radical polymn. gave a polymer [94060-32-9] contg. oxazoline pendant groups. The 2nd method was phase transfer-catalyzed etherification of poly(2,6-dimethyl-1,4-phenylene oxide) contg. pendant CH2Br groups with I. Incomplete etherification of bromobenzyl groups gave a polymer contg. cationically polymerizable heterocycles and their own cationic initiator as pendant groups.

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