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Detail of "18209-60-4"

  • CAS Number:
  • 18209-60-4
  • Name:
  • Silanamine,1-chloro-N,N,1,1-tetramethyl-

  • Molecular Structure:
  • Formula:
  • C4H12ClNSi
  • Molecular Weight:
  • 137.68
  • Synonyms:
  • Silylamine,1-chloro-N,N,1,1-tetramethyl- (6CI,7CI,8CI);(N,N-Dimethylamino)dimethylchlorosilane;Chloro(dimethylamino)dimethylsilane;Chlorodimethyl(dimethylamino)silane;
  • EINECS:
  • 242-095-3
  • Density:
  • 0.924 g/cm3
  • Boiling Point:
  • 85.1 °C at 760 mmHg
  • Flash Point:
  • 5.3 °C
  • Risk Codes:
  • 11-34
  • Safety:
  • 9-16-26-33 Details

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CAS No.18209-60-4 Silanamine,1-chloro-N,N,1,1-tetramethyl-

Assay:98%

Supplier:Hangzhou Dayangchem Co., Ltd. [ China (Mainland)]

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Tel:+86-571-88938639

Address:B/2601 Fuli Building, 328# WenEr Rd. Hangzhou City 310012 China

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CAS No.18209-60-4 Silanamine,1-chloro-N,N,1,1-tetramethyl-

Supplier:Beijing zhongke expanding chemical technology Co., LTD. [ China (Mainland)]

600Integral
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Tel:010-51600645 58608265;57131961

Address:Beijing changping area connects center north pearl tower 2 buildings

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Reference

Regioselective Synthesis of Polyfunctionalized Alkyltrisilanes and -Tetrasilanes via Reductive Cross-Coupling Reaction of Aminoalkylsilyl chlorides with Lithium
Regioselective Synthesis of Polyfunctionalized Alkyltrisilanes and -Tetrasilanes via Reductive Cross-Coupling Reaction of Aminoalkylsilyl chlorides with Lithium. Tamao, Kohei; Sun, Guang-Ri; Kawachi, Atsushi; Yamaguchi, Shigehiro (Institute for Chemical Research, Kyoto University, Uji 611, Japan). Organometallics, 16(4), 780-788 (English) 1997 American Chemical Society. CODEN: ORGND7. ISSN: 0276-7333.Some commonly used reagents like 90654-97-0 and 18209-60-4 are used in this experiment. DOCUMENT TYPE: Journal CA Section: 29 (Organometallic and Organometalloidal Compounds) Highly selective cross-coupling reactions promoted by Li metal were achieved between aminodichloromonosilanes R(Et2N)SiCl2 (R = Me, Et, Ph, Et2N) and 2 equiv of Me3SiCl (1) or (Et2N)Me2SiCl (2) and between aminochlorodisilanes (Et2N)nMe3-nSiSiMe(NEt2)Cl (n = 1, 2) and 1 equiv of 1, 2, or (Me2N)nR3-nSiCl (n = 1, R = Et; n = 2, R = Me, Et) in THF at room temp. to form the corresponding sym. and unsym. diamino- to pentaaminotrisilanes in high yields, which are transformed into alkoxy and fluoro derivs. under mild conditions. A tetraaminotetrasilane also was prepd. by reductive homocoupling of (Et2N)Me2SiSiMe(NEt2)Cl and converted into the alkoxytetrasilane. Some special exptl. procedures were employed for the selective coupling reactions. .
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