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2,2,4,4-tetra(propan-2-yl)-1,3,2,4-diazadisiletidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83312-34-9

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83312-34-9 Usage

Structure

Contains two silicon atoms bonded to two nitrogen atoms and two isopropyl groups, giving it a unique structure and chemical reactivity.

Use

High-performance catalyst in organic synthesis.

Applications

Production of polymers, pharmaceuticals, and agrochemicals.

Reactivity

Highly reactive compound that should be handled with care to avoid health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 83312-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,1 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83312-34:
(7*8)+(6*3)+(5*3)+(4*1)+(3*2)+(2*3)+(1*4)=109
109 % 10 = 9
So 83312-34-9 is a valid CAS Registry Number.

83312-34-9SDS

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 2,2,4,4-tetra(propan-2-yl)-1,3,2,4-diazadisiletidine

1.2 Other means of identification

Product number -
Other names 2,2,4,4-Tetraisopropylcyclodisilazan

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:83312-34-9 SDS

83312-34-9Relevant academic research and scientific papers

Four-membered Silicon-Nitrogen Rings - Synthesis and Reactions

Kliebisch, Ursula,Klingebiel, Uwe,Vater, Norbert

, p. 4561 - 4566 (2007/10/02)

Fluorosilylamines R2SiF-NH2, R = iPr (1), NMeSiMe3 (2), are obtained by the reaction of the difluorosilanes with LiNH2. 1 and 2 react with BuLi to give the corresponding lithium salts 1a and 2a.The LiF elimination from 1a leads to the formation of cyclodi

Acyclic and Cyclic NH-SiF Systems - Stepwise Condensation of (Fluorosilyl)amines

Klingebiel, Uwe,Vater, Norbert

, p. 3277 - 3282 (2007/10/02)

The stepwise synthesis of the cyclodi- and trisilazanes (R2SiNH)2,3 (3a,b, 4a,b) via acyclic compounds is achieved from difluorosilanes (R2SiF2) and LiNH2 (R = CHMe2, CMe3).From the reaction of tert butyltrifluorosilane with LiNH2, 3-,5-,7-,9-, and 11-membered compounds containing NHSiF chains (13, 14, 20, 22, 23) and the cyclic cis- and trans-trisilazanes (CMe3SiFNH)3 have been isolated.The reaction involves substitution, lithium exchange, and condensation.

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