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2-[Dimethyl(4-methylphenyl)silyl]phenylmethanol is an organic compound that belongs to the family of silanol alcohols. It is a colorless liquid with a molecular formula of C17H22OSi. This versatile chemical is characterized by its unique structure, which features a dimethylsilyl group attached to a phenyl ring, further connected to another phenyl ring through a methylene bridge. Its properties make it a valuable component in various scientific and industrial applications.

1217863-38-1

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1217863-38-1 Usage

Uses

Used in Organic Synthesis:
2-[Dimethyl(4-methylphenyl)silyl]phenylmethanol is used as a reagent in the field of organic synthesis for facilitating a range of chemical reactions. Its ability to participate in various reaction mechanisms, such as substitution, addition, and condensation, makes it a valuable asset in creating complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 2-[Dimethyl(4-methylphenyl)silyl]phenylmethanol is used as an effective intermediate in the synthesis of various drugs. Its unique structure allows for the development of new drug candidates with potential therapeutic applications, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Development:
Similarly, in the agrochemical sector, {2-[Dimethyl(4-methylphenyl)silyl]phenyl}methanol serves as an intermediate for the production of various agrochemicals. Its role in the synthesis of bioactive molecules can lead to the development of new pesticides, herbicides, and other agricultural products that can improve crop yield and protect against pests.
Used in Advanced Material Development:
The electronics and automotive industries have also benefited from the use of 2-[Dimethyl(4-methylphenyl)silyl]phenylmethanol. It has been utilized in the development of advanced materials with specific properties, such as high thermal stability, electrical conductivity, or mechanical strength, which are essential for the performance and reliability of electronic devices and automotive components.

Check Digit Verification of cas no

The CAS Registry Mumber 1217863-38-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,8,6 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1217863-38:
(9*1)+(8*2)+(7*1)+(6*7)+(5*8)+(4*6)+(3*3)+(2*3)+(1*8)=161
161 % 10 = 1
So 1217863-38-1 is a valid CAS Registry Number.

1217863-38-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H51691)  2-[Dimethyl(p-tolyl)silyl]benzyl alcohol, 97%   

  • 1217863-38-1

  • 1g

  • 466.0CNY

  • Detail
  • Alfa Aesar

  • (H51691)  2-[Dimethyl(p-tolyl)silyl]benzyl alcohol, 97%   

  • 1217863-38-1

  • 5g

  • 1862.0CNY

  • Detail

1217863-38-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-[dimethyl-(4-methylphenyl)silyl]phenyl]methanol

1.2 Other means of identification

Product number -
Other names AMTSi133

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:1217863-38-1 SDS

1217863-38-1Relevant articles and documents

Synthesis of HOMSi reagents by Pd/Cu-catalyzed silylation of bromoarenes with disilanes

Minami, Yasunori,Shimizu, Kenta,Tsuruoka, Chisato,Komiyama, Takeshi,Hiyama, Tamejiro

supporting information, p. 201 - 203 (2014/03/21)

Silylation of aryl bromides with disilanes of type {[2- (PGOCH2)C6H4]Me2Si}2 (PG: protecting group) successfully takes place in the presence of a Pd/Ruphos or Davephos/CuI catalytic system to afford HOMSi reagents containing various functional groups in good yields. BisHOMSi reagents were also prepared directly from the corresponding arylene dibromides.

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