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(2R 4R 5S)-(+)-2-CHLORO-3 4-DI-ME-5-PH-&, with the molecular formula C10H15Cl, is a chlorinated derivative featuring two methyl and one phenyl group attached to the carbon atoms. (2R 4R 5S)-(+)-2-CHLORO-3 4-DI-ME-5-PH-& possesses a chiral center and exhibits optical isomerism, existing in two non-superimposable mirror image forms. Its specific optical rotation and configuration of (2R, 4R, 5S) contribute to its unique stereochemical properties, making it a valuable compound in organic synthesis and pharmaceutical research.

28080-20-8

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28080-20-8 Usage

Uses

Used in Organic Synthesis:
(2R 4R 5S)-(+)-2-CHLORO-3 4-DI-ME-5-PH-& is utilized as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique stereochemistry allows for the creation of enantiomerically pure products, which is crucial for the development of pharmaceuticals and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (2R 4R 5S)-(+)-2-CHLORO-3 4-DI-ME-5-PH-& serves as a valuable compound for drug discovery and development. Its specific configuration and optical isomerism make it an ideal candidate for the synthesis of enantiomerically pure drug molecules, which can have significant implications for the efficacy and safety of medications.

Check Digit Verification of cas no

The CAS Registry Mumber 28080-20-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,8 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28080-20:
(7*2)+(6*8)+(5*0)+(4*8)+(3*0)+(2*2)+(1*0)=98
98 % 10 = 8
So 28080-20-8 is a valid CAS Registry Number.

28080-20-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,4R,5S)-(+)-2-Chloro-3,4-dimethyl-5-phenyl-1,3,2-oxazaphospholidine 2-sulfide

1.2 Other means of identification

Product number -
Other names -

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:28080-20-8 SDS

28080-20-8Downstream Products

28080-20-8Relevant academic research and scientific papers

Intermolecular effects on the radiogenic formation of electron-capture phosphorus-centered radicals. A single-crystal ESR study of diastereoisomeric precursors

Aagaard, Olav M.,Janssen, René A. J.,De Waal, Bas F. M.,Buck, Henk M.

, p. 938 - 944 (2007/10/02)

ESR experiments on X-irradiated single crystals of the 2R,4S,5R and 2S,4S,5R diastereoisomers of 2-chloro3,4-dimethyl-5-phenyl-1,3,2-oxazaphospholidine 2-sulfide reveal that the yield of radiogenic electron-capture reactions in the solid state strongly depends on intermolecular interactions in the crystal. In the present case a high yield of P-Cl three-electron-bond phosphoranyl radical anions is found in crystals of the 2R,4S,5R isomer, whereas no radical formation can be detected for the 2S,4S,5R isomer. An analysis of nonbonded interactions with neighboring molecules reveals that the geometry relaxation necessary for the radical stabilization is easily accommodated in crystals of the 2R,4S,5R isomer but not in the 2S,4S,5R isomer, explaining the observed difference in electron-capture efficiency. Experiments on radical formation in a MeTHF host matrix give further insight into the importance of the environment on radiogenic radical formation. The possible concurrent effect of the matrix on the electronic configuration and spin density distribution of the resulting phosphoranyl radical is discussed.

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