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2943-69-3

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2943-69-3 Usage

General Description

1,3-Bis(iodomethyl)tetramethyldisiloxane is a chemical compound with the molecular formula C6H18I2OSi2. It is a clear, colorless liquid that is used as a cross-linking agent in the production of silicone elastomers. 1,3-BIS(IODOMETHYL)TETRAMETHYLDISILOXANE contains two iodomethyl groups attached to a tetramethyldisiloxane backbone, making it a versatile building block for the synthesis of various silicone-based polymers and materials. It is also used in the production of adhesives, sealants, coatings, and other specialty silicone products due to its ability to improve the mechanical and thermal properties of silicone materials. Additionally, the presence of iodine atoms in the molecule allows for further chemical modification, making it a valuable component in the development of advanced silicone-based materials and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 2943-69-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2943-69:
(6*2)+(5*9)+(4*4)+(3*3)+(2*6)+(1*9)=103
103 % 10 = 3
So 2943-69-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H16I2OSi2/c1-10(2,5-7)9-11(3,4)6-8/h5-6H2,1-4H3

2943-69-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name iodomethyl-[iodomethyl(dimethyl)silyl]oxy-dimethylsilane

1.2 Other means of identification

Product number -
Other names 1,1,2,2-Tetramethyl-1,2-bis-chlormethyl-disiloxan

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:2943-69-3 SDS

2943-69-3Downstream Products

2943-69-3Relevant articles and documents

Greber,Metzinger

, p. 226,232 (1960)

Combined effect of ether and siloxane substituents on imidazolium ionic liquids

Chavan, Santosh N.,Mandal, Debaprasad

, p. 64821 - 64831 (2015/08/18)

Ionic liquids (ILs) in combination with ether and siloxane substituents on the imidazolium cation, comprising of bis(trifluoromethylsulfonyl)imide (NTf2) anions, have been synthesized due to their low viscosities, high thermal stabilities and low melting or glass transition temperatures(Tg). The structural flexibility of the ether and siloxane substituents on the imidazolium center overcomes the effect of van der Waals forces and gives them desirable and unique physical properties. These novel ILs show low viscosities (~72 mPa s at 25 °C), high thermal stabilities up to 430°C, and a wide liquid range over 500°C. In addition, these ILs exhibit only an amorphous glassy state on cooling at Tg below -74°C and cannot order properly to afford crystallization. The detailed thermal stability, phase transitions and heat capacity were studied by TGA, DSC and temperature-modulated DSC analysis. More importantly, we have also reported the large-scale (one kilogram) microwave-assisted synthesis of ILs [BMIM]Br and [1O2O2-Im-2O1]I as efficient and greener processes.

CARBON DIOXIDE ABSORBENT AND METHOD OF USING THE SAME

-

, (2012/01/12)

In accordance with one aspect, the present invention provides a composition which contains the amino-siloxane structures I, or III, as described herein. The composition is useful for the capture of carbon dioxide from process streams. In addition, the present invention provides methods of preparing the amino-siloxane composition. Another aspect of the present invention provides methods for reducing the amount of carbon dioxide in a process stream employing the amino-siloxane compositions of the invention, as species which react with carbon dioxide to form an adduct with carbon dioxide.

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