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1,1-Dichloro-2-(trimethylsilyl)cyclopropane is a chemical compound with the molecular formula C6H14Cl2Si. It is a colorless liquid at room temperature and is characterized by its cyclopropane ring structure, which consists of three carbon atoms bonded in a triangular arrangement. The compound features two chlorine atoms attached to the first carbon atom and a trimethylsilyl group (Si(CH3)3) attached to the second carbon atom. This unique structure endows the compound with specific chemical properties, making it useful in various applications, such as a protecting group in organic synthesis and a precursor in the synthesis of other organosilicon compounds. Due to its reactivity and potential hazards, it is essential to handle 1,1-Dichloro-2-(trimethylsilyl)cyclopropane with care and follow appropriate safety measures.

3591-38-6

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3591-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3591-38-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,9 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3591-38:
(6*3)+(5*5)+(4*9)+(3*1)+(2*3)+(1*8)=96
96 % 10 = 6
So 3591-38-6 is a valid CAS Registry Number.

3591-38-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,2-dichlorocyclopropyl)-trimethylsilane

1.2 Other means of identification

Product number -
Other names -

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

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More Details:3591-38-6 SDS

3591-38-6Downstream Products

3591-38-6Relevant academic research and scientific papers

GEM-DISILYLCYCLOPROPANES: PREPARATION ET UTILISATION EN SYNTHESE ORGANIQUE

Laguerre, Michel,Grignon-Dubois, Micheline,Dunogues, Jacques

, p. 1161 - 1169 (2007/10/02)

A simple general route for the conversion of olefins to gem-disilylcyclopropanes, involving the dichlorocyclopropanation of the double bond followed by silylation using the Me3SiCl/Li/THF reagent at 0-10 deg C, is described.Acetylation of bicyclic derivatives thus obtained constitutes an original synthesis of cycloalkylidene ketones by a process more convenient than those previously used, and also provides new acetyl dihydrofurans.

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