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944064-51-1

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944064-51-1 Usage

Description

2-[(4-Methoxyphenyl)dimethylsilyl]benzyl alcohol is a chemical compound that belongs to the class of benzyl alcohols. It is an organic compound containing a benzyl alcohol group attached to a dimethylsilyl group and a methoxyphenyl group. This unique structure endows it with versatile properties and applications in various fields.

Uses

Used in Organic Synthesis:
2-[(4-METHOXYPHENYL)DIMETHYLSILYL]BENZYL ALCOHOL is used as a versatile building block for the construction of various organic molecules and materials. Its ability to be easily modified and incorporated into larger structures makes it a valuable component in the synthesis of complex organic compounds.
Used in Materials Science:
In the field of materials science, 2-[(4-METHOXYPHENYL)DIMETHYLSILYL]BENZYL ALCOHOL is utilized for its unique structure and properties. It can contribute to the development of new materials with specific characteristics, such as improved stability, reactivity, or selectivity.
Used as a Protective Group in Chemical Reactions:
2-[(4-METHOXYPHENYL)DIMETHYLSILYL]BENZYL ALCOHOL serves as a protective group for alcohols in chemical reactions. This function is crucial in preventing unwanted side reactions and ensuring the desired product is formed with high selectivity.
Used in Pharmaceutical Synthesis:
As a reagent in the synthesis of pharmaceuticals, 2-[(4-METHOXYPHENYL)DIMETHYLSILYL]BENZYL ALCOHOL plays a significant role in the development of new drugs. Its unique structure can be leveraged to create molecules with specific biological activities, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical industry, 2-[(4-METHOXYPHENYL)DIMETHYLSILYL]BENZYL ALCOHOL is used as a reagent in the synthesis of various agrochemicals. Its incorporation into these compounds can lead to the development of more effective and targeted products for agricultural applications.
Used in Polymer Science:
2-[(4-METHOXYPHENYL)DIMETHYLSILYL]BENZYL ALCOHOL has potential applications in the field of polymers due to its unique structure and properties. It can be used to create novel polymers with specific characteristics, such as improved mechanical strength, thermal stability, or chemical resistance, which can be applied in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 944064-51-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,0,6 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 944064-51:
(8*9)+(7*4)+(6*4)+(5*0)+(4*6)+(3*4)+(2*5)+(1*1)=171
171 % 10 = 1
So 944064-51-1 is a valid CAS Registry Number.

944064-51-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H51662)  2-[(4-Methoxyphenyl)dimethylsilyl]benzyl alcohol   

  • 944064-51-1

  • 1g

  • 407.0CNY

  • Detail
  • Alfa Aesar

  • (H51662)  2-[(4-Methoxyphenyl)dimethylsilyl]benzyl alcohol   

  • 944064-51-1

  • 5g

  • 1529.0CNY

  • Detail

944064-51-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-[(4-methoxyphenyl)-dimethylsilyl]phenyl]methanol

1.2 Other means of identification

Product number -
Other names {2-[(4-Methoxy-phenyl)-dimethyl-silanyl]-phenyl}-methanol

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:944064-51-1 SDS

944064-51-1Relevant articles and documents

Improved Hiyama cross-coupling reactions using HOMSi

Marcuccio, Sebastian M.,Epa, Ruwan,Moslmani, Maisa,Hughes, Andrew B.

, p. 7178 - 7181 (2012/01/14)

Various parameters in the Hiyama cross-coupling reaction of HOMSi reagents with ethyl bromobenzoate were studied. These included solvent, ligand, palladium source, and added water. DMF and THF were found to be excellent solvents. Palladium chloride was found to be the best palladium source and no added water was required. The use of tri-o-tolylphosphine as the ligand proved to be particularly effective.

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