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(R)-(+)-t-Butyl 2-(p-Tolylsulfinyl)propionate, with the molecular formula C15H22O2S, is a chiral compound that possesses a non-superimposable mirror image. It is widely recognized for its role as an intermediate in organic synthesis, contributing to the preparation of pharmaceuticals, agrochemicals, and fragrances. Additionally, it serves as a chiral ligand in asymmetric catalysis and is instrumental in the synthesis of chiral building blocks and natural products. Its diverse applications and properties render it a valuable asset in the realm of organic chemistry and drug development.

83909-72-2

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83909-72-2 Usage

Uses

Used in Pharmaceutical Industry:
(R)-(+)-t-Butyl 2-(p-Tolylsulfinyl)propionate is used as an intermediate in the synthesis of various pharmaceuticals due to its unique chiral properties. It aids in the development of new drugs by providing a structural foundation that can be further modified to achieve desired therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical industry, (R)-(+)-t-Butyl 2-(p-Tolylsulfinyl)propionate is utilized as a key intermediate for the production of various agrochemicals. Its chiral nature allows for the creation of targeted and effective compounds that can be used in pest control and crop protection.
Used in Fragrance Industry:
(R)-(+)-t-Butyl 2-(p-Tolylsulfinyl)propionate is employed as an intermediate in the creation of fragrances. Its unique chemical structure enables the development of novel scents and contributes to the diversification of the fragrance market.
Used in Asymmetric Catalysis:
(R)-(+)-t-Butyl 2-(p-Tolylsulfinyl)propionate serves as a chiral ligand in asymmetric catalysis, a process that is crucial for the production of enantiomerically pure compounds. This application is particularly important in the synthesis of pharmaceuticals, where the stereochemistry of a molecule can significantly impact its biological activity.
Used in Synthesis of Chiral Building Blocks and Natural Products:
(R)-(+)-t-Butyl 2-(p-Tolylsulfinyl)propionate is used as a starting material in the synthesis of chiral building blocks and natural products. Its chiral nature allows for the creation of complex molecular structures with specific stereochemistry, which is essential for the development of new drugs and other bioactive compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 83909-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,0 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83909-72:
(7*8)+(6*3)+(5*9)+(4*0)+(3*9)+(2*7)+(1*2)=162
162 % 10 = 2
So 83909-72-2 is a valid CAS Registry Number.

83909-72-2SDS

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 Propanoic acid, 2-[(R)-(4-methylphenyl)sulfinyl]-, 1,1-dimethylethyl ester, (2R)-

1.2 Other means of identification

Product number -
Other names CH27475 (R)-(+)-T-BUTYL 2-(P-TOLYLSULFINYL)PROPIONATE

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:83909-72-2 SDS

83909-72-2Relevant academic research and scientific papers

SYNTHESIS OF POTENTIALLY ALLERGENIC CHIRAL α-(HYDROXYALKYL)ACRYLATES

Papageorgiou, Christos,Benezra, Claude

, p. 1303 - 1306 (1984)

The title componds have been synthesized with 75percent enantiomeric excess from chiral p-tolylsulfoxides 1 and aldehydes, followed by thermal elimination of the sulfoxide.

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