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Detail of "952-97-6"

  • MSDS Download
  • CAS Number:
  • 952-97-6
  • Name:
  • Benzene,1-nitro-4-(phenylthio)-

  • Molecular Structure:
  • Formula:
  • C12H9NO2S
  • Molecular Weight:
  • 231.27
  • Synonyms:
  • Sulfide,p-nitrophenyl phenyl (6CI,7CI,8CI);(4-Nitrophenyl)phenylsulphide;1-Nitro-4-(phenylthio)benzene;4-(Phenylthio)nitrobenzene;4-Nitro-1-(phenylthio)benzene;4-Nitrodiphenyl sulfide;4-Nitrophenyl phenylsulfide;NSC 87341;Phenyl 4-nitrophenyl sulfide;Phenyl p-nitrophenyl sulfide;p-Nitrodiphenyl sulfide;p-Nitrophenyl phenyl sulfide;
  • Density:
  • 1.31 g/cm3
  • Melting Point:
  • 52-55 °C(lit.)
  • Boiling Point:
  • 396.8 °C at 760mmHg
  • Flash Point:
  • 193.8 °C
  • Appearance:
  • yellow crystalline powder
  • Hazard Symbols:
  • IrritantXi
  • Risk Codes:
  • 36/37/38
  • Safety:
  • 26-36 Details

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CAS No.952-97-6 Benzene,1-nitro-4-(phenylthio)-

Supplier:Isotec [ United States]

10Integral
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Tel:1-937-859-1808

Address:3858 Benner Road Miamisburg, OH 45342

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Reference

Poly(styryldiphenylphosphine) as a deoxygenation reagent for sulfoxides
Poly(styryldiphenylphosphine) as a deoxygenation reagent for sulfoxides.Some chemicals with cas registry numbers like 952-97-6 are also used. Amos, Richard A. (Ohio Wesleyan Univ., Delaware, OH 43015, USA). J. Org. Chem., 50(8), 1311-13 (English) 1985. CODEN: JOCEAH. ISSN: 0022-3263. DOCUMENT TYPE: Journal CA Section: 25 (Benzene, Its Derivatives, and Condensed Benzenoid Compounds) Dialkyl, arylalkyl, and diaryl sulfoxides underwent redn. 952-97-6 are also occured in this study. to the corresponding sulfides when treated with polystyryldiphenylphosphine and CCl4 in a THF solvent. The reaction affords high yields (81-99%), is tolerant of a wide variety of functional groups, and is very convenient in terms of isolation of product. ..
Poly(styryldiphenylphosphine) as a deoxygenation reagent for sulfoxides
Poly(styryldiphenylphosphine) as a deoxygenation reagent for sulfoxides.Some chemicals with cas registry numbers like 952-97-6 are also used. Amos, Richard A. (Ohio Wesleyan Univ., Delaware, OH 43015, USA). J. Org. Chem., 50(8), 1311-13 (English) 1985. CODEN: JOCEAH. ISSN: 0022-3263. DOCUMENT TYPE: Journal CA Section: 25 (Benzene, Its Derivatives, and Condensed Benzenoid Compounds) Dialkyl, arylalkyl, and diaryl sulfoxides underwent redn. 952-97-6 are also occured in this study. to the corresponding sulfides when treated with polystyryldiphenylphosphine and CCl4 in a THF solvent. The reaction affords high yields (81-99%), is tolerant of a wide variety of functional groups, and is very convenient in terms of isolation of product. ..
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