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(E)-1-tert-butyl-2-(trimethylsilyl)diazene is an organic compound characterized by a diazenyl group (-N=N-) bonded to a tert-butyl group and a trimethylsilyl group. This molecule is a derivative of diazene, which is a diatomic molecule consisting of two nitrogen atoms. The presence of the tert-butyl group provides steric hindrance, while the trimethylsilyl group offers stability and reactivity to the molecule. (E)-1-tert-butyl-2-(trimethylsilyl)diazene is of interest in organic chemistry due to its potential applications in the synthesis of various organic compounds and its unique reactivity profile.

25811-66-9

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25811-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25811-66-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,1 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25811-66:
(7*2)+(6*5)+(5*8)+(4*1)+(3*1)+(2*6)+(1*6)=109
109 % 10 = 9
So 25811-66-9 is a valid CAS Registry Number.

25811-66-9SDS

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 tert-butyl(trimethylsilyl)diazene

1.2 Other means of identification

Product number -
Other names Diazene,(1,1-dimethylethyl)(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

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More Details:25811-66-9 SDS

25811-66-9Relevant academic research and scientific papers

Transition-Metal-Free Silylation of Unactivated C(sp2)-H Bonds withtert-Butyl-Substituted Silyldiazenes

Neil, Baptiste,Lucien, Franck,Fensterbank, Louis,Chauvier, Clément

, p. 13085 - 13090 (2021/11/01)

Aromatic organosilanes bearing C(sp2)-Si bonds have found increasing applications across the chemical science, yet are mostly produced by atom-uneconomical stoichiometric procedures. Catalytic alternatives using hydrosilanes as silicon sources

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