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Phosphonic acid, [(3R)-3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-oxobutyl]-, dimethyl ester is a complex organic compound that falls under the category of phosphonic acids and their derivatives. It features a dimethyl ester functional group attached to a phosphonic acid backbone, which is further substituted with a 3-oxobutyl chain and a bulky tert-butylphenyldiphenylsilyloxy group. This unique molecular architecture endows it with versatile reactivity and stability, making it a valuable component in various chemical processes and applications.

162582-63-0

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162582-63-0 Usage

Uses

Used in Catalysts:
Phosphonic acid, [(3R)-3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-oxobutyl]-, dimethyl ester serves as a catalyst in numerous chemical reactions due to its ability to stabilize intermediates and transition states. Its phosphonic acid functionality can coordinate with metal centers, facilitating catalysis in various organic transformations.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, Phosphonic acid, [(3R)-3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-oxobutyl]-, dimethyl ester acts as a key building block for the synthesis of complex organic molecules with potential therapeutic applications. Its unique structure allows for the creation of novel drug candidates with improved pharmacokinetic and pharmacodynamic properties.
Used in Agrochemical Production:
Phosphonic acid, [(3R)-3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-oxobutyl]-, dimethyl ester is also utilized in the development of agrochemicals, contributing to the synthesis of new pesticides and herbicides with enhanced efficacy and selectivity.
Used in Flame Retardants:
Phosphonic acid,
[(3R)-3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-oxobutyl]-, dimethyl ester's thermal stability and reactivity make it suitable for use in the production of flame retardants, which are essential for improving the fire safety of various materials, including plastics and textiles.
Used in Plasticizers:
Its compatibility with polymers and ability to enhance the flexibility and processability of plastics make it a valuable component in the formulation of plasticizers, which are additives used to improve the performance of plastic materials.
Used in Specialty Chemicals:
Due to its unique chemical properties, Phosphonic acid, [(3R)-3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-oxobutyl]-, dimethyl ester finds application in the production of specialty chemicals, which are often used in niche applications such as coatings, adhesives, and sealants.
Used in Organic Synthesis and Chemical Research:
Phosphonic acid,
[(3R)-3-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-oxobutyl]-, dimethyl ester's versatility and reactivity make it a valuable tool in organic synthesis and chemical research, where it can be used to explore new reaction pathways and develop innovative synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 162582-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,5,8 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 162582-63:
(8*1)+(7*6)+(6*2)+(5*5)+(4*8)+(3*2)+(2*6)+(1*3)=140
140 % 10 = 0
So 162582-63-0 is a valid CAS Registry Number.

162582-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl (3R)-3-((tert-butyl(diphenyl)silyl)oxy)-2-oxobutylphosphonate

1.2 Other means of identification

Product number -
Other names [(R)-3-(tert-Butyl-diphenyl-silanyloxy)-2-oxo-butyl]-phosphonic acid dimethyl ester

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:162582-63-0 SDS

162582-63-0Relevant academic research and scientific papers

A 1,2-O-O-SILYL-MIGRATION-CLAISEN-REARRANGEMENT-SN2'-DISPLACEMENT SEQUENCE IN THE STEREOSELECTIVE SYNTHESIS OF 5-OXAPROSTANOID DERIVATIVES

Mulzer, Johann,Greifenberg, Stefan

, p. 93 - 96 (2007/10/02)

A novel stereocontrolled route to 5-oxaprostaglandin and PGF intermediates is described, which starts from the ene-diols (6/7) and uses a sequence of Claisen rearrangement, 1,2-O-O-silyl migration and SN2'-cyclization reactions (9b10a/b via

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