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Detail of "4867-37-2"

  • MSDS Download
  • CAS Number:
  • 4867-37-2
  • Name:
  • 3-Chlorothioanisole

  • Molecular Structure:
  • Formula:
  • C7H7ClS
  • Molecular Weight:
  • 158.64
  • Synonyms:
  • Sulfide,m-chlorophenyl methyl (6CI,7CI,8CI);3-(Methylthio)-1-chlorobenzene;3-Chlorophenyl methyl sulfide;Methyl 3-chlorophenylsulfide;Methyl m-chlorophenyl sulfide;NSC 133796;m-Chlorophenyl methylsulfide;m-Chlorothioanisole;
  • Density:
  • 1.2 g/cm3
  • Boiling Point:
  • 217.9 °C at 760 mmHg
  • Flash Point:
  • 87.6 °C
  • Hazard Symbols:
  • IrritantXi
  • Risk Codes:
  • 22-36/37/38
  • Safety:
  • 23-36/37-36-26 Details

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CAS No.4867-37-2 3-Chlorothioanisole

3-Chloro thioanisole

Supplier:zhejiang shou&fu chemical co., ltd [ China (Mainland)]

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ManufacturerBS-OHSASISO 2725Integral
2725

Tel:+86-571-88902507

Address:5/F, Yangfan Venture Plaza, 31 Xincheng Road, Binjiang District , Hangzhou City, Zhejiang Province,310051,P.R. China

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CAS No.4867-37-2 3-Chlorothioanisole

Supplier:Hangzhou TJM Chemical Trade Co., Ltd [ China (Mainland)]

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960Integral
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Tel:86-571-88223276 86-13388471767

Address:2221#,Boyuexuan,1860# Binsheng Road,Binjiang District, Hangzhou CityZhejiang Province, 310051, P. R. China

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Reference

Excited state electron transfer reactions of tris(2,2'-bipyridine)chromium(III) ion with organic sulfides
Excited state electron transfer reactions of tris(2,2'-bipyridine)chromium(III) ion with organic sulfides. Gnanaraj, G. Allen; Rajagopal, S.; Srinivasan, C. (Sch. Chem., Madurai Kamaraj Univ., Madurai 625 021, India). Proc. - Indian Acad. Sci., Chem. Sci., 104(1), 9-13 (English) 1992. CODEN: PIAADM. 623-13-2 and 4867-37-2 are also in the experiment. ISSN: 0253-4134. DOCUMENT TYPE: Journal CA Section: 67 (Catalysis, Reaction Kinetics, and Inorganic Reaction Mechanisms) Section cross-reference(s): 74 The quenching rate consts., kq, for the excited state electron transfer reactions of tris(2,2'-bipyridine)chromium(III) ion with several aryl Me sulfides (ArSMe) obtained by the luminescence quenching technique, are accelerated by electron releasing groups and retarded by electron withdrawing groups present in the aryl moiety of ArSMe. The plot of RT 1nkq vs. E1/2 values of different sulfides is linear, indicating the electron transfer nature of the reaction. Studies with alkyl Ph sulfides demonstrate the importance of the steric effect in these photoredox reactions. .
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