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19752-23-9

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19752-23-9 Usage

General Description

Cinnamyltrimethylsilane is an organic compound that belongs to the group of silanes. It is colorless and has a characteristic odor. This chemical is commonly used as a synthetic intermediate and is versatile in organic synthesis. It is utilized in the production of fragrances, flavors, and pharmaceuticals. Cinnamyltrimethylsilane can also act as a reagent in organic reactions, particularly in the formation of carbon-carbon bonds. Its unique chemical structure and reactivity make it a valuable compound in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 19752-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,5 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19752-23:
(7*1)+(6*9)+(5*7)+(4*5)+(3*2)+(2*2)+(1*3)=129
129 % 10 = 9
So 19752-23-9 is a valid CAS Registry Number.

19752-23-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl(3-phenylprop-2-enyl)silane

1.2 Other means of identification

Product number -
Other names 3-phenylallyltrimethylsilane

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:19752-23-9 SDS

19752-23-9Relevant articles and documents

A convenient synthesis of z-allylsilanes with good stereoselectivity promoted by samarium diiodide

Concellón, José M.,Rodríguez-Solla, Humberto,Simal, Carmen,Gómez, Cecilia

, p. 75 - 78 (2007)

Synthesis of Z-allylsilanes in high or good yields and with good stereoselectivity is achieved from O-acetylated 1-silyl-3-chloro alcohols promoted by SmI2. The starting compounds were easily prepared from 2-chloroaldehydes and a mechanism is p

Three-Component Visible-Light-Induced Palladium-Catalyzed 1,2-Alkyl Carbamoylation/Cyanation of Alkenes

Jia, Xiangqing,Zhang, Ziyan,Gevorgyan, Vladimir

, p. 13217 - 13222 (2021/11/01)

A mild visible-light-induced Pd-catalyzed one-pot three-component alkyl-carbamoylation and cyanation of alkenes was developed. This general transformation, which proceeds via the in situ formation of a reactive ketenimine intermediate, allows for a rapid construction of a broad range of valuable amides and nitriles from readily available alkenes, alkyl iodides, and isocyanides. An efficient synthesis of tetrazole and amidine via this approach was also demonstrated.

METHOD FOR PRODUCING ALLYLSILANE COMPOUND UTILIZING PALLADIUM NANOPARTICLE CATALYST

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Paragraph 0062-0097; 0101, (2020/11/24)

PROBLEM TO BE SOLVED: To provide a method for efficiently producing an allylsilane compound from a substrate being inexpensive and capable of being easily handled in one step without using a large amount of a metal catalyst. SOLUTION: The method for producing an allylsilane compound represented by formula (C) includes a reaction step of reacting an allyl alcohol compound represented by formula (A) and a disilane compound represented by formula (B) in the presence of a palladium nanoparticle catalyst having a coordinating organic compound coordinated to the surface of a palladium nanoparticle and a co-catalyst. (In formulae (A) to (C), R1 to R3 each independently represent a hydrogen atom, a 1-20C aliphatic hydrocarbon group, a 6-20C aromatic hydrocarbon group or a 3-20C aromatic heterocyclic group; R4 and R5 each independently represent a hydrogen atom, 1-20C aliphatic hydrocarbon group, a 6-20C aromatic hydrocarbon group or a 3-20C aromatic heterocyclic group; and R6 to R8 each independently represent a hydrogen atom, a halogen atom, a 1-20C aliphatic hydrocarbon group or a 6-20C aromatic hydrocarbon group.) SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

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