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:
C- Risk Codes:
- 34-43-21/22
- Safety:
- 26-36/37/39-45Details
- Transport Information:
- UN 3265 8/PG 3
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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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