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17988-51-1

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17988-51-1 Usage

Description

(3-ethylphenyl)(trimethyl)silane, also known as ethyl(trimethylsilyl)benzene, is a silane derivative with the molecular formula C11H18Si. It is a colorless liquid with a faint odor and is highly flammable. (3-ethylphenyl)(trimethyl)silane is commonly used as a reagent in organic synthesis and as a protective group for alcohols and amines, making it a valuable tool for chemists in the preparation of complex organic molecules.

Uses

Used in Organic Synthesis:
(3-ethylphenyl)(trimethyl)silane is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions and improve the efficiency of the synthesis process.
Used in Protective Group Chemistry:
(3-ethylphenyl)(trimethyl)silane is used as a protective group for alcohols and amines, allowing chemists to temporarily block certain functional groups during the synthesis of complex organic molecules, preventing unwanted side reactions.
Used in Pharmaceutical Industry:
(3-ethylphenyl)(trimethyl)silane is used in the production of fine and specialty chemicals, as well as in the pharmaceutical industry, for its role in the synthesis of pharmaceutical compounds and the development of new drugs.
Used in Agrochemical Industry:
(3-ethylphenyl)(trimethyl)silane is used in the agrochemical industry for its involvement in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural chemicals.
Used in Silicone-based Materials Manufacturing:
(3-ethylphenyl)(trimethyl)silane is used in the manufacturing of silicone-based materials, which have a wide range of applications in various industries, including construction, electronics, and personal care products.
Used in Synthesis of Organosilicon Compounds:
(3-ethylphenyl)(trimethyl)silane is used in the synthesis of other organosilicon compounds, which have diverse applications in industries such as electronics, automotive, and aerospace.

Check Digit Verification of cas no

The CAS Registry Mumber 17988-51-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,8 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17988-51:
(7*1)+(6*7)+(5*9)+(4*8)+(3*8)+(2*5)+(1*1)=161
161 % 10 = 1
So 17988-51-1 is a valid CAS Registry Number.

17988-51-1SDS

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 3-Trimethylsilyl-aethylbenzol

1.2 Other means of identification

Product number -
Other names m-Aethyl-benzolboronsaeure

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:17988-51-1 SDS

17988-51-1Relevant articles and documents

UNE VOIE ORIGINALE ET SELECTIVE DE FONCTIONNALISATION EN POSITION META DU FLUORO- ET DE L'ETHYLBENZENE

Bennetau, Bernhard,Krempp, Michele,Dunogues, Jacques,Ratton, Serge

, p. 8131 - 8142 (2007/10/02)

An original and regioselective method for the meta functionalisation of fluoro- and ethylbenze is reported.This process involves a 2,5-disilylation of these subtrates using trimethylchlorosilane in the presence of lithium in THF as the solvent.After aromatisation, monodesilylation in position 2- and electrophilic substitution of the trimethylsilyl group in position 5-, meta acetyl-, senecioyl-, benzoyl-, and iodofluorobenzenes and ethylbenzenes as well as the sodium salts of metafluoro or meta ethylbenzenesulfonic acid and 3-aminosulfonylfluorobenzene were obtained in good yields. pair of diastereomeric triamines 15 and 16.A tricyclic diazasystem 19 was formed from the reaction of cyanide with the carbamoylated chloroenamine 18.Monochloroenamine 10a and dichloroenamine 12a showed a significant mutagenic behaviour in the Ames test.

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