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Cyclohexanol, 2-[[3-(trimethylsilyl)-2-propynyl]oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62343-69-5

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62343-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62343-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,4 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62343-69:
(7*6)+(6*2)+(5*3)+(4*4)+(3*3)+(2*6)+(1*9)=115
115 % 10 = 5
So 62343-69-5 is a valid CAS Registry Number.

62343-69-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-trimethylsilylprop-2-ynoxy)cyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names Cyclohexanol,2-[[3-(trimethylsilyl)-2-propynyl]oxy]

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:62343-69-5 SDS

62343-69-5Downstream Products

62343-69-5Relevant academic research and scientific papers

Organic electrosynthesis using toluates as simple and versatile radical precursors

Lam, Kevin,Marko, Istvan E.

supporting information; experimental part, p. 95 - 97 (2009/03/11)

The electrolysis of toluate esters leads smoothly to the formation of the radical of the alkyl fragment. This property has been used to develop a new electrochemical deoxygenation reaction. The Royal Society of Chemistry.

Toluates: unexpectedly versatile reagents

Lam, Kevin,Markó, István E.

supporting information; experimental part, p. 10930 - 10940 (2010/02/28)

The mechanism of the monoelectronic reduction of aromatic esters has been investigated. The unexpected synthetic utility of the toluate moiety in the deoxygenation of alcohols and the allylation of ketones is also reported. Finally, the use of aromatic esters as robust, though easily removable, protecting groups is depicted.

Using toluates as simple and versatile radical precursors

Lam, Kevin,Marko, Istvan E.

supporting information; experimental part, p. 2773 - 2776 (2009/05/30)

(Chemical Equation Presented) The viability of the toluate moiety as a radical precursor has been examined by studying deoxygenation and cyclization reactions.

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