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Detail of "39319-11-4"

  • CAS Number:
  • 39319-11-4
  • Name:
  • Diphenyl(4-vinylphenyl)phosphine-divinylbenzene-styrene copolymer

  • Molecular Structure:
  • Formula:
  • (C20H17P)m.(C10H10)n.(C8H8)x
  • Molecular Weight:
  • 262.285461
  • Synonyms:
  • 4-DIPHENYLPHOSPHINO POLYSTYRENE RESIN;COPOLYMER OF STYRENE AND DIVINYLBENZENE, DIPHENYLPHOSPHINATED;DIPHENYLPHOSPHINOBENZOYL NOVAGEL(TM) AM RESIN;DIPHENYLPHOSPHINO-POLYSTYRENE;MACROPOROUS POLYMER SUPPORTED TRIPHENYLPHOSPHINE;PL-TPP RESIN;PL-TPP MP-RESIN;POLYMER SUPPORTED TRIPHENYLPHOSPHINE
  • Hazard Symbols:
  • Risk Codes:
  • R22;R43   
  • Safety:
  • Hazard Codes Xn,Xi
    Risk Statements 22-43-20/21/22-36/37/38
    Safety Statements 36/37-36-26
    WGK Germany 3
    10-23
    Details

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CAS No.39319-11-4 Diphenyl(4-vinylphenyl)phosphine-divinylbenzene-styrene copolymer

storage temp. : 2-8°C Hazard Codes : Xn Risk Statements : 22-43 Safety Statements : 36/37 WGK Germany : 3 F : 10-23

Supplier:POLYMERLABS [ United Kingdom]

136Integral
136

Tel:+44 1694 723581

Address:Amherst Fields Research Park 160 Old Farm Road Amherst MA 01002 USA

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CAS No.39319-11-4 Diphenyl(4-vinylphenyl)phosphine-divinylbenzene-styrene copolymer

Supplier:Zhengzhou Alfachem Co., Ltd. [ China (Mainland)]

600Integral
600

Tel:0371-55616343

Address:zhengzhou

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Reference

Highly crosslinked polymeric reagents
Highly crosslinked polymeric reagents. Polymer-supported phosphines and their use in the conversion of alcohols to chloroalkanes. Sherrington, D. C.; Craig, D. J.; Dagleish, J.; Domin, G.; Taylor, J.; Meehan, G. V. (Dep. Pure Appl. Chem., Univ. Strathclyde, Glasgow, Scot.). Eur. Polym. J., 13(2), 73-6 (English) 1977. CODEN: EUPJAG. DOCUMENT TYPE: Journal CA Section: 35 (Synthetic High Polymers) Section cross-reference(s): 23 Divinylbenzene-styrene-styryldiphenylphosphine copolymer (I) [39319-11-4] samples were prepd. by suspension polymn. with crosslink d. 15, 25, and 37%, and 3 other samples with crosslink d. 37% were prepd. in the presence of PhMe at PhMe-monomer ratios 0.5-2:1. In CCl4 alcs. were converted to chloroalkanes by I in yields which decreased with increase in crosslink d. and increased with increase in PhMe-monomer ratio. Results indicate that a degree of substrate selectivity is achieved by varying crosslink d. I, crosslink d. 15%, gave results similar to those of similar P-contg. polymers of crosslink d. 1-2%. A mechanism was given, involving reaction of 2 equiv of P with 1 equiv of alc., thus showing a degree of mobility of the crosslinked chains.
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