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Detail of "4217-66-7"

  • MSDS Download
  • CAS Number:
  • 4217-66-7
  • Name:
  • 1,2-Propanediol,2-phenyl-

  • Superlist Name:
  • 2-Phenyl-1,2-propanediol
  • Molecular Structure:
  • Formula:
  • C9H12 O2
  • Molecular Weight:
  • 152.19
  • Deleted CAS:
  • 87760-50-7
  • Synonyms:
  • (?à)-1-Methyl-1-phenyl-1,2-ethanediol;(?à)-2-Phenyl-1,2-propanediol;2-Phenyl-1,2-propanediol; 2-methyl-2-phenylethane-1,2-diol; NSC 51067
  • EINECS:
  • 224-154-5
  • Melting Point:
  • 44-45 ºC
  • Boiling Point:
  • 160-162 ºC (26 mmHg)
  • Flash Point:
  • 113 ºC

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CAS No.4217-66-7 2-Phenyl-1,2-propanediol

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Reference

Examples of triphase reactions involving a crosslinked polymer, a solid, and a liquid phase
Examples of triphase reactions involving a crosslinked polymer, a solid, and a liquid phase. Hodge, Philip; Khoshdel, Ezzatollah; Waterhouse, Janette (Dep. Chem., Univ. Lancaster, Bailrigg LA1 4YA, UK). Makromol. Chem., 185(3), 489-97 (English) 1984. CODEN: MACEAK.There are some reagents with their cas registry numbers 1100-88-5 and 629-27-6 are used in this study. ISSN: 0025-116X. DOCUMENT TYPE: Journal CA Section: 35 (Chemistry of Synthetic High Polymers) Section cross-reference(s): 38 Several reactions involving crosslinked polymers, a solid, and a liq. phase were investigated. Wittig reactions between crosslinked polymers contg. phosphonium salt residues, solid K2CO3, and aldehydes in THF proceeded satisfactorily, even in the absence of a phase-transfer catalyst. The oxidn. of 2-phenyl-1,2-propanediol [4217-66-7] in CH2Cl2 by solid NaIO4 (but not KIO4) was catalyzed by the periodate form of an anion exchange resin. The reaction of 1-bromooctane [111-83-1] in benzene, THF, or MeCN with KCN or NaCN and of benzyl bromide [100-39-0] in THF or MeCN with KOAc or NaOAc were catalyzed only slightly, if at all, by the cyanide or acetate forms of an anion exchange resin. Crosslinked polymers contg. crown ether residues catalyzed the reaction of 1-bromooctane in PhMe with NaI. It was not clear how the crosslinked polymers and solid reagents managed to react with each other, but possible mechanisms were discussed. The importance of carrying out control reactions in such studies was stressed. .
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