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62244-48-8

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62244-48-8 Usage

Description

Methoxy(4-methoxyphenyl)dimethylsilane is an organosilicon compound characterized by a clear colorless liquid appearance. It is composed of a methoxy group, a 4-methoxyphenyl group, and two methyl groups attached to a central silicon atom. This unique structure endows it with specific chemical properties that make it suitable for various applications in different industries.

Uses

Used in Mechanistic Studies:
Methoxy(4-methoxyphenyl)dimethylsilane is used as a reagent in the mechanistic study of arylsilane oxidation. Its unique structure allows for the investigation of the oxidation process and the understanding of the underlying chemical reactions, which can be crucial for the development of new synthetic methods and applications in organic chemistry.
Used in Chemical Synthesis:
In the field of chemical synthesis, Methoxy(4-methoxyphenyl)dimethylsilane can be employed as an intermediate or a building block for the synthesis of more complex organic molecules. Its organosilicon nature and the presence of the methoxy and 4-methoxyphenyl groups make it a versatile compound for the creation of a wide range of chemical products.
Used in Material Science:
Methoxy(4-methoxyphenyl)dimethylsilane may also find applications in material science, particularly in the development of new materials with specific properties. Its organosilicon structure can contribute to the formation of novel materials with enhanced characteristics, such as improved thermal stability, mechanical strength, or chemical resistance.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Methoxy(4-methoxyphenyl)dimethylsilane could be utilized in the design and synthesis of new drug candidates. Its unique chemical structure may provide novel interactions with biological targets, potentially leading to the development of new therapeutic agents with improved efficacy and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 62244-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,4 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62244-48:
(7*6)+(6*2)+(5*2)+(4*4)+(3*4)+(2*4)+(1*8)=108
108 % 10 = 8
So 62244-48-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O2Si/c1-11-9-5-7-10(8-6-9)13(3,4)12-2/h5-8H,1-4H3

62244-48-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H28625)  Methoxy(4-methoxyphenyl)dimethylsilane, 97%   

  • 62244-48-8

  • 1g

  • 458.0CNY

  • Detail
  • Alfa Aesar

  • (H28625)  Methoxy(4-methoxyphenyl)dimethylsilane, 97%   

  • 62244-48-8

  • 5g

  • 1284.0CNY

  • Detail

62244-48-8SDS

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 methoxy-(4-methoxyphenyl)-dimethylsilane

1.2 Other means of identification

Product number -
Other names Methoxy(4-methoxyphenyl)dimethylsilane

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:62244-48-8 SDS

62244-48-8Downstream Products

62244-48-8Relevant articles and documents

Synthesis of phenols via fluoride-free oxidation of arylsilanes and arylmethoxysilanes

Rayment, Elizabeth J.,Summerhill, Nick,Anderson, Edward A.

, p. 7052 - 7060 (2012/10/07)

Rapid, efficient methods have been developed to prepare phenols from the oxidation of arylhydrosilanes. The effects of arene substituents and fluoride promoters on this process show that while electron-deficient arenes can undergo direct oxidation from the hydrosilane, electron-rich aromatics benefit from silane activation via oxidation to the methoxysilane using homogeneous or heterogeneous transition metal catalysis. The combination of these two oxidations into a streamlined flow procedure involving minimal processing of reaction intermediates is also reported.

Electrochemical method for the production of organofunctional silanes

-

Page/Page column 4, (2008/06/13)

Organofunctional silanes are prepared in high yield by electrochemically reacting a silane bearing a halo or alkoxy group with a hydrocarbon bearing a halo or alkoxy group in an undivided electrolysis cell with no or minimal complexing agent present.

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