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138585-09-8

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138585-09-8 Usage

Description

4-(tert-Butyldimethylsilyloxy)benzyl chloride is an organic chemical compound characterized by the molecular formula C14H25ClOSi. It is a derivative of benzyl chloride, distinguished by the replacement of a hydrogen atom on the benzene ring with a 4-(tert-butyldimethylsilyloxy) group. This modification endows the compound with unique properties that are valuable in various chemical processes.

Uses

Used in Organic Synthesis:
4-(tert-Butyldimethylsilyloxy)benzyl chloride serves as a protecting group for alcohols, crucial for preventing unwanted side reactions at the hydroxyl group during chemical reactions. This function is particularly important in complex organic synthesis processes where selectivity and control over reaction outcomes are paramount.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 4-(tert-Butyldimethylsilyloxy)benzyl chloride is utilized as a reagent for the introduction of the benzyl group into organic compounds. The benzyl group can improve the solubility, stability, or biological activity of the resulting pharmaceutical compounds, making this chemical an essential tool in drug development.
Used in Agrochemical Synthesis:
Similarly, in agrochemical synthesis, 4-(tert-Butyldimethylsilyloxy)benzyl chloride is applied to introduce the benzyl group into various compounds. This can enhance the effectiveness, selectivity, or environmental compatibility of agrochemical products, contributing to the advancement of safer and more efficient crop protection agents.
Used in the Synthesis of Fine Chemicals:
4-(tert-Butyldimethylsilyloxy)benzyl chloride also finds application in the synthesis of fine chemicals, where its ability to protect alcohols and introduce benzyl groups is leveraged to create specialty chemicals with specific properties required in various industries, such as fragrances, dyes, or advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 138585-09-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,8 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 138585-09:
(8*1)+(7*3)+(6*8)+(5*5)+(4*8)+(3*5)+(2*0)+(1*9)=158
158 % 10 = 8
So 138585-09-8 is a valid CAS Registry Number.

138585-09-8SDS

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 tert-butyl-[4-(chloromethyl)phenoxy]-dimethylsilane

1.2 Other means of identification

Product number -
Other names 4-(TERT-BUTYLDIMETHYLSILYLOXY)BENZYL CHLORIDE

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:138585-09-8 SDS

138585-09-8Relevant articles and documents

FLUOROCHROME-COUPLED COELENTERAZINE

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, (2017/02/02)

PROBLEM TO BE SOLVED: To provide techniques of making the light emission wavelength of a Renilla luciferase (Rluc)-coelenterazine light-emitting system longer by modifying coelenterazine. SOLUTION: A fluorochrome-coupled coelenterazine is represented by t

Bioluminescent coelenterazine derivatives with imidazopyrazinone C-6 extended substitution

Nishihara, Ryo,Suzuki, Hideyuki,Hoshino, Emi,Suganuma, Sakura,Sato, Moritoshi,Saitoh, Tsuyoshi,Nishiyama, Shigeru,Iwasawa, Naoko,Citterio, Daniel,Suzuki, Koji

, p. 391 - 394 (2015/02/19)

Three novel coelenterazine (CTZ) derivatives with extension at the C-6 position of the imidazopyrazinone structure show significant bioluminescence emission with known renilla luciferase variants, indicating a promising method to develop CTZ derivatives w

COELENTERAZINE ANALOGUES AND COELENTERAMIDE ANALOGUES

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, (2014/10/29)

Coelenterazine analogs with different luminescence properties from conventional ones and coelenteramide analogs with different fluorescence properties from conventional ones have been desired. The invention provides coelenterazine analogs modified at the

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