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Detail of "10169-55-8"

  • MSDS Download
  • CAS Number:
  • 10169-55-8
  • Name:
  • Ethanone,1-[4-(phenylthio)phenyl]-

  • Superlist Name:
  • 4-Acetyldiphenyl sulfide
  • Molecular Structure:
  • Formula:
  • C14H12OS
  • Molecular Weight:
  • 228.31
  • Synonyms:
  • Acetophenone,4'-(phenylthio)- (6CI,7CI,8CI);1-[4-(Phenylthio)phenyl]ethan-1-one;4-(Phenylthio)acetophenone;4-Acetyldiphenyl sulfide;4-Acetylphenyl phenylsulfide;4'-(Phenylsulfanyl)acetophenone;4'-(Phenylthio)acetophenone;NSC158592;p-(Phenylthio)acetophenone;p-Acetylphenyl phenyl sulfide;
  • Density:
  • 1.17 g/cm3
  • Melting Point:
  • 67-68 °C
  • Boiling Point:
  • 389.6 °C at 760 mmHg
  • Flash Point:
  • 215 °C
  • Risk Codes:
  • 20/21/22
  • Safety:
  • 23-36/37/39 Details

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CAS No.10169-55-8 4-Acetyldiphenyl sulfide

4-Acetyldiphenyl sulfide

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.10169-55-8 4-Acetyldiphenyl sulfide

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

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Supplier
960Integral
960

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

Energy sensitive acid generating agents for energy curable compositions
Energy sensitive acid generating agents for energy curable compositions. Kanno, Masaki; Uesugi, Takahiko; Matsumoto, Shigehiro (Toyo Ink Mfg. Co., Ltd., Japan). Jpn. Kokai Tokkyo Koho JP 2005075945 A2 24 Mar 2005, 65 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: ICM: C09K003-00. ICS: C07C381-12; C07D333-46; G03F007-004. APPLICATION: JP 2003-308671 1 Sep 2003. DOCUMENT TYPE: Patent CA Section: 35 (Chemistry of Synthetic High Polymers) Section cross-reference(s): 38, 42, 74 The present invention relates to energy sensitive acid generating agents I, wherein R1, R2, R3, R4, R5 = H, alkyl, aryl, alkenyl, acyl, alkoxy, aryloxy, acyloxy, alkoxycarbonyloxy, halogen, or SR31 (31 of them is SR31); R31 = alkyl or aryl; R11, R12 = H, alkyl, aryl, alkoxy, or alkenyl; R21, R22 = alkyl, aryl, ir alkenyl; and X = anion (R1, R2, R3, R4, R5, R12, R22, R21, and R11 may form a ring together). Thus, 50.0 g diphenylsulfide and 20.95 g acetyl chloride were reacted in carbon disulfide at 25° for 4 h, 20.0 g of the resulting p-(phenylthio)acetophenone was reacted with 41.4 g tetrabutylammonium bromide for 3 h at room temp. to give p-(phenylthio)phenacylbromide, 24.8 g of which was reacted with 10.1 g dimethylsulfide, 24.9 g of the resulting dimethyl[(p-phenylthio)phenacyl]sulfonium bromide was mixed with 1151 g 4.00% sodium tetrakis(pentafluorophenyl)borate soln. 10169-55-8 which is the cas registry number of some chemical is mentioned. to give dimethyl[(p-phenylthio)phenacyl]sulfonium tetrakis(pentafluorophenyl)borate, 0.6 mmol of which was mixed with 10 g UVR 6110 (acid curable compd.),, applied on an aluminum plate, and irradiated with a metal halide lamp to give a cured film with tack free. .
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