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N-(Dichloroboryl)hexamethyldisilazane is a chemical compound with the formula [(CH3)3Si]2NBCl2. It is a colorless, hygroscopic liquid that is sensitive to air and moisture. N-(DICHLOROBORYL)HEXAMETHYLDISILAZANE is primarily used as a reagent in organic synthesis, particularly in the formation of boron-nitrogen bonds. It serves as a source of the dichloroboryl group, which can be used to introduce boron atoms into organic molecules. The compound is also known for its ability to act as a Lewis acid, facilitating various chemical transformations. Due to its reactivity, it is typically handled under an inert atmosphere and is stored away from heat and light to maintain its stability.

6591-26-0

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6591-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6591-26-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,9 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6591-26:
(6*6)+(5*5)+(4*9)+(3*1)+(2*2)+(1*6)=110
110 % 10 = 0
So 6591-26-0 is a valid CAS Registry Number.

6591-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name [[dichloroboranyl(trimethylsilyl)amino]-dimethylsilyl]methane

1.2 Other means of identification

Product number -
Other names Boranamine,1,1-dichloro-N,N-bis(trimethylsilyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:6591-26-0 SDS

6591-26-0Relevant academic research and scientific papers

Dehydrohalogenation and cleavage reactions in silicon-nitrogen-boron systems

Wells, Richard L.,Collins, Alva L.

, p. 1327 - 1328 (2007/10/14)

Two sets of reaction conditions have been found where a dehydrohalogenation reaction occurred when triethylamine-boron trichloride adduct was allowed to react with hexamethyldisilazane. In one case both dehydrohalogenation and cleavage occurred, resulting in the formation of a novel unsymmetrical N-silyl-substituted aminohalogenoborane. Under the other set of conditions an N-silyl-substituted aminodihalogenoborane was produced as a result of only dehydrohalogenation.

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