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69657-20-1

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69657-20-1 Usage

Type of compound

Organosilicon compound

Structure

Five-membered silicon ring (silole derivative)

Substituents

Two ethyl groups attached to the silicon atom

Category

1,1-diethyl-2,5-dihydro-1H-silole

Interest in materials chemistry

Due to unique electronic and optical properties

Potential applications

a. Organic light-emitting diodes (OLEDs)
b. Organic photovoltaics
c. Organic field-effect transistors

Relevance in semiconductor industry

Electronic and optical properties make it a candidate for various applications

Chemical properties and reactivity

Determine specific properties and potential applications of the compound

Check Digit Verification of cas no

The CAS Registry Mumber 69657-20-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,5 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69657-20:
(7*6)+(6*9)+(5*6)+(4*5)+(3*7)+(2*2)+(1*0)=171
171 % 10 = 1
So 69657-20-1 is a valid CAS Registry Number.

69657-20-1SDS

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 1,1-diethyl-2,5-dihydrosilole

1.2 Other means of identification

Product number -
Other names diethylsilacyclopentene

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:69657-20-1 SDS

69657-20-1Downstream Products

69657-20-1Relevant articles and documents

Arene-Catalysed Lithiation of 1,4-Dichlorobut-2-enes and 3,4-Dichlorobut-1-ene and Reaction with Electrophiles: A Common Reaction Pathway

Guijarro, Albert,Yus, Miguel

, p. 7857 - 7864 (1994)

The reaction of (Z) or (E)-1,4-dichlorobut-2-ene (1, 2), or 3,4-dichlorobut-1-ene (3) with an excess of lithium powder and a catalytic amount of 4,4'-di-tert-butylbiphenyl (5 molpercent) in the presence of an electrophile tCHO, Me3SiCl> in THF at 0 deg C yields, after hydrolysis, the corresponding 1,4- and 1,2-disubstituted compounds (Z/E)-4 and 5, the ratio of them being independent on the starting material.In the case of compounds 4 the Z-diastereomer is largely the major one.When dichlorodiethylsilane was used as electrophile the corresponding substituted silacyclopentene 6 was the only reaction product isolated.A possible mechanism involving dilithiated species is proposed.

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