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2943-62-6

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2943-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2943-62-6 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 2943-62:
(6*2)+(5*9)+(4*4)+(3*3)+(2*6)+(1*2)=96
96 % 10 = 6
So 2943-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H15ClOSi2/c1-8(2,3)7-9(4,5)6/h1-5H3

2943-62-6SDS

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 Chloropentamethyldisiloxane

1.2 Other means of identification

Product number -
Other names -

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:2943-62-6 SDS

2943-62-6Relevant articles and documents

Greber et al.

, p. 87,93 (1962)

New achiral phenylacetylene monomers having an oligosiloxanyl group most suitable for helix-sense-selective polymerization and for obtaining good optical resolution membrane materials

Liu, Lijia,Zang, Yu,Hadano, Shingo,Aoki, Toshiki,Teraguchi, Masahiro,Kaneko, Takashi,Namikoshi, Takeshi

scheme or table, p. 9268 - 9276 (2011/11/14)

To develop new phenylacetylene monomers more suitable for helix-sense-selective polymerization (HSSP) we reported previously and to improve the efficiency of the HSSP and membrane performance of the resulting polymers, novel phenylacetylenes having a flexible oligosiloxanyl group (SnBDHPA)together with the other related three series of monomers were synthesized and polymerized by using a chiral catalytic system and enantioselectivity in permeation of the membranes from the resulting chiral polymers were examined. SnBDHPA was the most suitable for the HSSP and the CD absorptions (G values) of poly- (SnBDHPA) were stronger and more stable than those of the corresponding polymers having rigid alkyl groups. The polymers could be fabricated to flexible self-supporting membranes by using solvent-casting method. In addition, enantioselectivity in permeation of one of poly(SnBDHPA) membranes was much higher than that of a poly(phenylacetylene) membrane having alkyl groups. This was because the polymers having oligosiloxane groups had high regularity of structures, i.e., chemical structures of the macromolecules such as one handedness and high order structures such as columnar contents in the membranes, and the membranes were flexible and had almost no defects. These good properties as optical resolution membrane materials were caused by flexibility, hydrophobicity, and bulkiness of the oligosiloxane chains. S3BDHPA having a trisiloxanyl group was found to be the best monomer for the HSSP and for obtaining good optical resolution membrane materials.

Surface Active Organosilicone Compounds

-

Page/Page column 6-7, (2008/12/09)

The present invention relates to new organodisilanes or carbodisilanes, a process for manufacturing the same and their use, in particular, as surface active agents, especially as spreading agents.

Reaction of the dioxane complex of dichlorogermylene with siloxanes

Shcherbinin,Pushkina,Krivolapova,Bykovchenko,Khromykh,Komalenkova,Chernyshev

, p. 1907 - 1910 (2007/10/03)

The major organogermanium compounds formed by reactions of the dioxane complex of dichlorogermylene with hexamethyldisiloxane, octamethyltrisiloxane, and hexamethyltricyclotrisiloxane are bis(trimethylsiloxy)dichlorogermane, 3,3-dichloro-1,1,1,5,5,7,7,7-o

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