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Silane, (4-ethynylphenyl)dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

244307-32-2

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244307-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 244307-32-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,4,3,0 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 244307-32:
(8*2)+(7*4)+(6*4)+(5*3)+(4*0)+(3*7)+(2*3)+(1*2)=112
112 % 10 = 2
So 244307-32-2 is a valid CAS Registry Number.

244307-32-2SDS

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 (p-(dimethylsilyl)phenyl)acetylene

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:244307-32-2 SDS

244307-32-2Downstream Products

244307-32-2Relevant academic research and scientific papers

Synthesis, in-situ membrane preparation, and good gas permselectivity of insoluble poly(substituted acetylene)s loosely cross-linked with short and soft siloxane and silanol linkages

Wang, Jianjun,Aoki, Toshiki,Kaneko, Takashi,Teraguchi, Masahiro

, (2019/12/25)

Insoluble but membrane-formable poly(substituted acetylene)s loosely cross-linked by short and soft Si–O–Si and SiOH---(OH)Si linkages have been synthesized from the corresponding monomers having one or two SiOH groups. These monomers have been polymerized in homogeneous systems to produce homogeneous polymer solutions in toluene. The resulting solutions were cast on polytetrafuluoroethylene sheets followed by evaporation of the solvent to give tough and flexible membranes which were completely insoluble. The membranes showed good oxygen and carbon oxide permselectivity and their plots in PO2 vs PO2/PN2 graph exceeded the 1991 Robeson's upper bound and very close to the 2008 Robeson's upper bound. The excellent selectivity are caused by enhancement of diffusion selectivity by the soft network structure which can create small pores (i.e., ultramicro pores) based on the short linkages. No drop in permeability may be due to the soft Si–O–Si and SiOH---(OH)Si linkages. In addition no change in PO2 and PO2/PN2 by aging was observed.

Heme Protein Catalysts for Carbon-Silicon Bond Formation In Vitro and In Vivo

-

Paragraph 0269, (2017/08/26)

The present invention provides compositions and methods for catalyzing the formation of carbon-silicon bonds using heme proteins. In certain aspects, the present invention provides heme proteins, including variants and fragments thereof, that are capable of carrying out in vitro and in vivo carbene insertion reactions for the formation of carbon-silicon bonds. In other aspects, the present invention provides methods for producing an organosilicon product, the method comprising providing a silicon-containing reagent, a carbene precursor, and a heme protein; and combining the components under conditions sufficient to produce an organosilicon product. Host cells expressing the heme proteins are also provided by the present invention.

Synthesis of silicon-containing unsaturated polymers by hydrosilylation reaction. Photophysical studies

Wang, Fei,Kaafarani, Bilal R.,Neckers, Douglas C.

, p. 8225 - 8230 (2007/10/03)

Silicon-containing unsaturated polymers have been synthesized using the Pt(acac)2-catalyzed photoactivated hydrosilylation of alkynes. These polymers fluoresce at 360 nm when excited at 270 nm due to the π-conjugated vinylphenyl segment in the polymer chain. The polymers have excellent solubility in several organic solvents.

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