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18001-76-8

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18001-76-8 Usage

Type of compound

Organosilicon compound

Structure

Contains two silicon atoms, each bonded to two methyl groups and two ethoxy groups

Physical state

Colorless liquid

Uses

a. Precursor in the synthesis of other organosilicon compounds
b. Reagent in organic chemistry reactions
c. Production of silicone polymers and resins
d. Semiconductor industry for thin film formation
e. Protective coating for electronic components

Applications

Industrial and research applications due to unique properties and reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 18001-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,0 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18001-76:
(7*1)+(6*8)+(5*0)+(4*0)+(3*1)+(2*7)+(1*6)=78
78 % 10 = 8
So 18001-76-8 is a valid CAS Registry Number.

18001-76-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [diethoxy(methyl)silyl]-diethoxy-methylsilane

1.2 Other means of identification

Product number -
Other names 1,1,2,2-Tetraethoxy-1,2-dimethyldisilane

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:18001-76-8 SDS

18001-76-8Relevant articles and documents

Une synthese originale et rapide de (methyldiethoxysilyl)benzenes fonctionnels

Cros, S.,Bennetau, B.,Dunogues, J.,Babin, P.

, p. 69 - 74 (2007/10/02)

In the presence of a catalytic amount of tetrakis(triphenylphosphine)palladium(0), the 1,1,2,2-tetraethoxydimethyldisilane reacts with various functional bromoarenes giving the corresponding aryldiethoxymethylsilanes in good yields.The creation of Si-CAr bonds involving a polyalcoxydisilane as the silylating reagent is here reported for the first time.Key words: Silyl; Palladium

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