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999-97-3

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999-97-3 Usage

Chemical Description

Hexamethyldisilazane, trimethylchlorosilane, and pyridine are used to prepare the silylating reagent, which is used to treat the residue after the fractions are collected.

Check Digit Verification of cas no

The CAS Registry Mumber 999-97-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,9 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 999-97:
(5*9)+(4*9)+(3*9)+(2*9)+(1*7)=133
133 % 10 = 3
So 999-97-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H19NSi2/c1-8(2,3)7-9(4,5)6/h7H,1-6H3

999-97-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (H0089)  1,1,1,3,3,3-Hexamethyldisilazane  >96.0%(GC)

  • 999-97-3

  • 10mL

  • 80.00CNY

  • Detail
  • TCI America

  • (H0089)  1,1,1,3,3,3-Hexamethyldisilazane  >96.0%(GC)

  • 999-97-3

  • 25mL

  • 100.00CNY

  • Detail
  • TCI America

  • (H0089)  1,1,1,3,3,3-Hexamethyldisilazane  >96.0%(GC)

  • 999-97-3

  • 100mL

  • 195.00CNY

  • Detail
  • TCI America

  • (H0089)  1,1,1,3,3,3-Hexamethyldisilazane  >96.0%(GC)

  • 999-97-3

  • 500mL

  • 430.00CNY

  • Detail
  • Alfa Aesar

  • (A15139)  Hexamethyldisilazane, 98+%   

  • 999-97-3

  • 25ml

  • 190.0CNY

  • Detail
  • Alfa Aesar

  • (A15139)  Hexamethyldisilazane, 98+%   

  • 999-97-3

  • 100ml

  • 322.0CNY

  • Detail
  • Alfa Aesar

  • (A15139)  Hexamethyldisilazane, 98+%   

  • 999-97-3

  • 500ml

  • 806.0CNY

  • Detail
  • Alfa Aesar

  • (A15139)  Hexamethyldisilazane, 98+%   

  • 999-97-3

  • 2500ml

  • 3210.0CNY

  • Detail
  • Alfa Aesar

  • (42039)  Hexamethyldisilazane, Electronic grade, 99+%   

  • 999-97-3

  • 25g

  • 290.0CNY

  • Detail
  • Alfa Aesar

  • (42039)  Hexamethyldisilazane, Electronic grade, 99+%   

  • 999-97-3

  • 100g

  • 312.0CNY

  • Detail
  • Alfa Aesar

  • (42039)  Hexamethyldisilazane, Electronic grade, 99+%   

  • 999-97-3

  • 500g

  • 1409.0CNY

  • Detail
  • Alfa Aesar

  • (L16519)  Hexamethyldisilazane, Electronic grade, 99+%   

  • 999-97-3

  • 25ml

  • 251.0CNY

  • Detail

999-97-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name hexamethyldisilazane

1.2 Other means of identification

Product number -
Other names SILAZANE HMN

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Adhesives and sealant chemicals,CBI,Intermediates
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:999-97-3 SDS

999-97-3Relevant articles and documents

-

Wannagat,U. et al.

, p. 373 - 384 (1970)

-

The Instability of Ni{N(SiMe3)2}2: A Fifty Year Old Transition Metal Silylamide Mystery

Faust, Michelle,Bryan, Aimee M.,Mansikkam?ki, Akseli,Vasko, Petra,Olmstead, Marilyn M.,Tuononen, Heikki M.,Grandjean, Fernande,Long, Gary J.,Power, Philip P.

, p. 12914 - 12917 (2015)

The characterization of the unstable NiII bis(silylamide) Ni{N(SiMe3)2}2 (1), its THF complex Ni{N(SiMe3)2}2(THF) (2), and the stable bis(pyridine) derivative trans-Ni{N(SiMe3)2}2(py)2 (3), is described. Both 1 and 2 decompose at ca. 25°C to a tetrameric NiI species, [Ni{N(SiMe3)2}]4 (4), also obtainable from LiN(SiMe3)2 and NiCl2(DME). Experimental and computational data indicate that the instability of 1 is likely due to ease of reduction of NiII to NiI and the stabilization of 4 through dispersion forces.

Deoxygenation of primary amides to amines with pinacolborane catalyzed by Ca[N(SiMe3)2]2(THF)2

Gong, Mingliang,Guo, Chenjun,Jiang, Linhong,Luo, Yunjie,Yu, Chong

supporting information, p. 1201 - 1206 (2021/05/29)

Deoxygenative reduction of amides is a challenging but favorable synthetic method of accessing amines. In the presence of a catalytic amount of Ca[N(SiMe3)2]2(THF)2, pinacolborane (HBpin) could efficiently reduce a broad scope of amides, primary amides in particular, into corresponding amines. Functional groups and heteroatoms showed good tolerance in this process of transformation, and a plausible reaction mechanism was proposed.

Preparation method of silazane

-

Paragraph 0020-0021, (2020/10/14)

The invention provides a preparation method of silazane. The preparation method comprises the following steps: carrying out a stirring reaction on monochlorosilane, alkali metal amide, a catalyst anda solvent in a reaction container completely; and after the reaction is finished, carrying out reduced pressure distillation to obtain the silazane. Compared with the prior art, the invention providesa new silazane synthesis technology, the process is simple, the yield is as high as 93.0%, and the purity can reach 93.6%.

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