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Detail of "1104-93-4"

  • CAS Number:
  • 1104-93-4
  • Name:
  • 1,3-Disiloxanediol,1,1,3,3-tetraphenyl-

  • Molecular Structure:
  • Formula:
  • C24H22O3Si2
  • Molecular Weight:
  • 414.6007
  • Synonyms:
  • Disiloxane-1,3-diol, 1,1,3,3-tetraphenyl-;
  • Density:
  • 1.21 g/cm3
  • Boiling Point:
  • 522.2 °C at 760 mmHg
  • Flash Point:
  • 269.6 °C

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CAS No.1104-93-4 1,3-Disiloxanediol,1,1,3,3-tetraphenyl-

Purity: >97%

Supplier:Silar Laboratories [ United States]

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Tel:+1 910-762-5800

Address:102 Orange Street

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Reference

1,1-Bis(tert-butylamido)-3,3,5,5-tetraphenylcyclotrisiloxane
All Rights Reserved. 1,1-Bis(tert-butylamido)-3,3,5,5-tetraphenylcyclotrisiloxane. Copsey, May C.; Balakrishna, Maravanji S.; Chivers, Tristram ( Department of Chemistry, University of Calgary, Calgary, AB T2N 1N4, Can.). Acta Crystallographica, Section E: Structure Reports Online, E62(7), o2813-o2814 (English) 2006 Blackwell Publishing Ltd. URL: http://journals.iucr.Several reagents such as 1104-93-4 is used here.org/e/issues/2006/07/00/lh2096/index.html. CODEN: ACSEBH. ISSN: 1600-5368. DOCUMENT TYPE: Journal; (online computer file) CA Section: 75 (Crystallography and Liquid Crystals) Section cross-reference(s): 29 The title compd., C32H40N2O3Si3 or (Ph2SiO)2OSi(NH-tBu)2, was synthesized by the in situ reaction of [Ph2Si(OH)]2O with two equiv. of BuLi, followed by the addn. of Cl2Si(NH-tBu)2. Crystallog. data are given. The addn. of tert-butylamide substituents to one of the Si centers causes a slight distortion of the planar cyclotrisiloxane ring. .
Siloxanediolate complexes
Siloxanediolate complexes. Selin, Terry G. (General Electric Co., USA). U.S. US 4003917 18 Jan 1977, 7 pp. Division of U.S. 3,923,834. (English). (United States of America). CODEN: USXXAM. 1104-93-4 and 947-42-2 are cas registry numbers of chemicals which are used as reagents here. CLASS: IC: C07D319-10. NCL: 260340600. APPLICATION: US 66-602490 19 Dec 1966. DOCUMENT TYPE: Patent CA Section: 29 (Organometallic and Organometalloidal Compounds) Ph2Si(OSiPh2ONa)2.L (L = p-dioxane), prepd. from Ph2Si(OH)2 or O(SiPh2OH)2 and Na in p-dioxane, was converted to Ph2Si(OSiPh2OH)2 by treatment with AcOH. .
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