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Benzenesulfonamide, N,N-bis(trimethylsilyl)-, also known as N,N-bis(trimethylsilyl)benzenesulfonamide, is an organosilicon compound with the chemical formula C9H21NO2SSi2. It is a white crystalline solid that is soluble in common organic solvents. Benzenesulfonamide, N,N-bis(trimethylsilyl)- is primarily used as a reagent in organic synthesis, particularly in the protection of amines and as a silylating agent. It is also employed in the preparation of various organosilicon compounds and as a precursor in the synthesis of other benzenesulfonamide derivatives. Due to its unique properties, it has applications in the pharmaceutical, chemical, and materials science industries.

1023-95-6

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1023-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1023-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1023-95:
(6*1)+(5*0)+(4*2)+(3*3)+(2*9)+(1*5)=46
46 % 10 = 6
So 1023-95-6 is a valid CAS Registry Number.

1023-95-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-bis(trimethylsilyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N,N-di(trimethylsilyl)benzenesulfonamide

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:1023-95-6 SDS

1023-95-6Relevant academic research and scientific papers

Tetrasubstituted Tetrazenes (Me3E)2N-N=N-N(EMe3)2 (E = Si, Ge, Sn): Reactivity

Wiberg, Nils,Bayer, Heiner,Vasisht, Sham Kumar,Meyers, Rene

, p. 2916 - 2927 (2007/10/02)

By substitution of the silyl, germyl, or stannyl groups, (Me3Si)2N-N=N-N(SiMe3)2 (1) reacts with variable amounts of trifluoroacetic acid to form (Me3Si)4-nN4Hn, (Me3Ge)2N-N=N-N(GeMe)2 (2) with variable amounts of methanol to form (Me3Ge)4-nN4Hn, and (Me3Sn)2N-N=N-N(SnMe3)2 (3) with variable amounts of trimethylchlorosilane to give (Me3Sn)4-nN4(SiMe3)n (n = 1-4).The reaction of 1 with benzenesulfonyl isocyanate leads by substitution and cyclization to silylated 5-hydroxytetrazole 12.Substitution in connection with thermolysis of the substitution products formed is found in the reaction of 1 with methanol, aluminium chloride, or nitrosyl chloride and in the reaction of 3 with trimethylstannane, acetone, or nitrosobenzene.By oxidation of 1 with chlorine, bromine, or p-benzoquinone and of 3 with p-benzoquinone or oxygen, all tetrazene nitrogen is envolved.The reduction of 1 with hydrogen or alkali metals leads to nitrogen and (Me3Si)2NH or (Me3Si)2NM.

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