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17937-68-7

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17937-68-7 Usage

Description

DIPHENYLDIVINYLSILANE, with the molecular formula C20H20Si, is an organosilicon compound characterized by the presence of two phenyl groups and two vinyl groups attached to a central silicon atom. This versatile chemical serves as a crucial precursor in the synthesis of a range of silicon-containing polymers and materials, particularly in the creation of silicone-based compounds.

Uses

Used in Silicone Polymer Synthesis:
DIPHENYLDIVINYLSILANE is utilized as a precursor in the production of various silicon-containing polymers. Its unique structure allows for the formation of a wide array of silicone-based materials, which are known for their thermal stability, flexibility, and resistance to environmental degradation.
Used in Silicone Rubber and Elastomers Production:
As a crosslinking agent, DIPHENYLDIVINYLSILANE plays a vital role in the manufacturing process of silicone rubbers and elastomers. Its ability to form stable crosslinks contributes to the development of materials with enhanced mechanical properties and improved performance in various applications.
Used in Organic Synthesis:
DIPHENYLDIVINYLSILANE is also employed in organic synthesis, where it serves as a reagent for the formation of carbon-silicon bonds in a variety of chemical reactions. This capability broadens its utility in the synthesis of complex organic molecules and contributes to the development of new compounds with potential applications in various industries.
Used in Chemical Research:
In the field of chemical research, DIPHENYLDIVINYLSILANE is used as a model compound to study the properties and reactions of organosilicon compounds. Its unique structure and reactivity provide valuable insights into the behavior of silicon-containing molecules and contribute to the advancement of silicon chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 17937-68-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,3 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17937-68:
(7*1)+(6*7)+(5*9)+(4*3)+(3*7)+(2*6)+(1*8)=147
147 % 10 = 7
So 17937-68-7 is a valid CAS Registry Number.

17937-68-7SDS

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 DIPHENYLDIVINYLSILANE

1.2 Other means of identification

Product number -
Other names DIVINYLDIPHENYLSILANE

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:17937-68-7 SDS

17937-68-7Relevant articles and documents

Synthesis and structural characterization of trans-tactic vinylene-silylene(siloxylene) polymers

Marciniec, Bogdan,Mallecka, Ewa

, p. 818 - 823 (2003)

A new synthetic route to prepare stereoselectively trans-tactic poly[vinylene-silylene(siloxylene)]s via polycondensation of divinyldiorganosilanes and divinyltetraorganodisiloxanes in the presence of [{RuCl2(CO)3}2] as a

CAPPED DUAL-HEADED ORGANOALUMINUM COMPOSITIONS

-

Paragraph 0120, (2019/07/17)

The present disclosure relates to a capped dual-headed organoaluminum composition having the formula (I) and processes to prepare the same. In at least one aspect, the capped dual-headed organoaluminum compositions can be used in olefin polymerization.

Diphenylsilyldiethylene- (DPSide-) group: A new primary amine protection

Kim, B. Moon,Cho, Jong Hyun

, p. 5333 - 5336 (2007/10/03)

Diphenylsilydiethylene- (DPSide-) group has been developed as a new primary amine protecting group. The new protecting group exhibits novel orthogonality against other commonly used amine-protecting groups and excellent chemoselectivity for unbranched α-amino acid esters. Removal of this protecting group was effected under mild fluoride-based cleavage conditions.

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