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18026-87-4

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18026-87-4 Usage

General Description

1,1,1-trichloro-2,2,2-trimethyldisilane is a chemical compound with the molecular formula C3H9Cl3Si2. It is a clear, colorless liquid that is highly volatile and flammable. 1,1,1-trichloro-2,2,2-trimethyldisilane is commonly used as a reagent in organic synthesis, particularly in the production of silicon-based polymers and materials. It is also utilized as a building block in the manufacturing of various silicon compounds, such as silanes and silicone resins. In addition, 1,1,1-trichloro-2,2,2-trimethyldisilane is known for its potential as a high-performance solvent and as a surface coating for metal and glass to improve their adhesion properties. However, it is important to handle this chemical with caution, as it is harmful if swallowed, inhaled, or absorbed through the skin, and may cause irritation to the respiratory system and skin upon exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 18026-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,2 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18026-87:
(7*1)+(6*8)+(5*0)+(4*2)+(3*6)+(2*8)+(1*7)=104
104 % 10 = 4
So 18026-87-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H9Cl3Si2/c1-7(2,3)8(4,5)6/h1-3H3

18026-87-4SDS

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 1,1,1-Trichloro-2,2,2-trimethyldisilane

1.2 Other means of identification

Product number -
Other names Disilane, 1,1,1-trichloro-2,2,2-trimethyl-

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:18026-87-4 SDS

18026-87-4Relevant articles and documents

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Hengge,E. et al.

, p. 887 - 892 (1975)

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Preparation of oligosilanes containing perhalogenated silyl groups (-SiX3, -SiX2-, >SiX-, X = Cl, Br) and their hydrogenation by stannanes

Herzog,Roewer

, p. 217 - 223 (2007/10/03)

Starting from methylphenylsubstituted oligosilanes the disilanes SiX3-SiXi,Me3-i (i = 0, 1, 2; X = Cl, Br), trisilanes SiX2(SiXiMe3-i) (i = 0, 1) and branched tetrasilanes SiX(SiXMe2)3 were synthesized and their behavior towards the Lewis-base catalyzed hydrogenation by stannanes was investigated. In the case of methylchlorodisilanes SiCl3-SiCliMe3-i Si-Si bond cleavage competes with the hydrogenation reaction.

Eine neue Methode zur Darstellung von funktionell substituierten Oligosilanen

Uhlig, Wolfram,Tzschach, Alfred

, p. 335 - 336 (2007/10/02)

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