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Detail of "14470-28-1"

  • MSDS Download
  • CAS Number:
  • 14470-28-1
  • Name:

  • Benzene,1-(chlorodiphenylmethyl)-4-methoxy-

  • Superlist Name:
  • 4-Methoxytriphenylmethyl chloride
  • Molecular Structure:
  • Formula:
  • C20H17ClO
  • Molecular Weight:
  • 308.81
  • Synonyms:
  • Anisole,p-(chlorodiphenylmethyl)- (6CI,7CI,8CI);1-(Chlorodiphenylmethyl)-4-methoxybenzene;4-Anisyl(chloro)diphenylmethane;4-Methoxytrityl chloride;Mono-p-methoxytrityl chloride;NSC 54121;p-(Chlorodiphenylmethyl)anisole;p-Methoxytritylchloride;
  • EINECS:
  • 238-463-8
  • Density:
  • 1.151 g/cm3
  • Melting Point:
  • 122-124 °C(lit.)
  • Boiling Point:
  • 426.8 °C at 760 mmHg
  • Flash Point:
  • 208.4 °C
  • Appearance:
  • light orange powder
  • Hazard Symbols:
  • IrritantXi,CorrosiveC
  • Risk Codes:
  • 36/37/38-34
  • Safety:
  • 26-36-45-36/37/39 Details
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CAS No.14470-28-1 4-Methoxytriphenylmethyl chlorideCompetitive Product

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CAS No.14470-28-1 4-Methoxytriphenylmethyl chloride

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CAS No.14470-28-1 4-Methoxytriphenylmethyl chloride

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CAS No.14470-28-1 4-Methoxytriphenylmethyl chloride

4-Methoxytriphenylchloromethane,cas#14470-28-1

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CAS No.14470-28-1 4-Methoxytriphenylmethyl chloride

Benzene,1-(chlorodiphenylmethyl)-4-methoxy-

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CAS No.14470-28-1 4-Methoxytriphenylmethyl chloride

4-Methoxytrityl chloride

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4-Methoxytriphenylchloromethane

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4-Methoxytrityl chloride

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Reference

Synthesis of the novel bicyclic oxepinopyrimidine and fluorinated pyrrolidinopyrimidines
Synthesis of the novel bicyclic oxepinopyrimidine and fluorinated pyrrolidinopyrimidines.Several substances are used for example 14470-28-1 and 820966-03-8 which are their cas registry numbers. Batinac, Sanja; Sermek, Draginja Mrvos; Cetina, Mario; Pavelic, Kresimir; Mintas, Mladen; Raic-Malic, Silvana (Department of Organic Chemistry, Faculty of Chemical Engineering and Technology, Zagreb HR-10000, Croatia). Heterocycles, 63(11), 2523-2536 (English) 2004 Japan Institute of Heterocyclic Chemistry. CODEN: HTCYAM. ISSN: 0385-5414. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Section cross-reference(s): 26 The new 5,6-disubstituted pyrimidine nucleoside analogs, e.g. I, were synthesized by addn. of the C-6 lithiated pyrimidine deriv. to oxirane as key reaction step. The bicyclic tetrahydrooxepinopyrimidine (II) and fluorinated pyrrolidinopyrimidines were obtained by intramol. linkage of acyclic chain to the CH2-5 and N-1 of the pyrimidine ring. The structure of II contg. pyrimidine and tetrahydrooxepine skeleton was detd. unequivocally by its X-ray crystal structure anal. .
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