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1-Pyrrolidinecarboxylic acid, 2-[3-[(methylsulfonyl)oxy]propyl]-3-[[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (2R,3S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

849112-01-2

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849112-01-2 Usage

Molecular structure

1-Pyrrolidinecarboxylic acid, 2-[3-[(methylsulfonyl)oxy]propyl]-3-[[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (2R,3S)is an ester derivative of pyrrolidinecarboxylic acid with a bulky tert-butyl ester group attached.

Stereochemistry

The compound has a specific stereochemistry with a 2R,3S configuration, which is important for its biological activity and potential therapeutic applications.

Pharmaceutical research and development

1-Pyrrolidinecarboxylic acid, 2-[3-[(methylsulfonyl)oxy]propyl]-3-[[(phenylmethoxy)carbonyl]amino]-, 1,1-dimethylethyl ester, (2R,3S)- is often used as a building block in the synthesis of various drugs and pharmaceuticals, as well as in chemical and biological research.

Potential pharmacological properties

Due to its unique structure and stereochemistry, the compound has garnered interest and attention from the scientific and medical community for its potential pharmacological properties and applications.

Tert-butyl ester group

The presence of a bulky tert-butyl ester group in the structure contributes to the compound's stability and reactivity in chemical reactions.

Carbonyl and amino groups

The presence of carbonyl and amino groups in the structure allows for various chemical reactions and modifications, making it a versatile building block in drug synthesis.

Ester functional group

The ester group in the compound can undergo hydrolysis reactions, which can be important for the release and absorption of the compound in biological systems.

Potential therapeutic applications

Due to its unique structure and properties, the compound may have potential applications in the treatment of various diseases and conditions, although further research is needed to determine its efficacy and safety.

Check Digit Verification of cas no

The CAS Registry Mumber 849112-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,1,1 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 849112-01:
(8*8)+(7*4)+(6*9)+(5*1)+(4*1)+(3*2)+(2*0)+(1*1)=162
162 % 10 = 2
So 849112-01-2 is a valid CAS Registry Number.

849112-01-2Relevant academic research and scientific papers

A flexible carbanionic approach to protected trans-(2R,3S)-2-substituted 3-aminopyrrolidines: Application to the asymmetric synthesis of (+)-absouline

Tang, Tian,Ruan, Yuan-Ping,Ye, Jian-Liang,Huang, Pei-Qiang

, p. 231 - 234 (2007/10/03)

Based on the use of phenyl thioether (3S)-7 as a synthetic equivalent to the N- and α-dianions (3S)-2a, a new carbanionic approach to trans-(2R,3S)-2-substituted 3-aminopyrrolidines (10) is described. Application of the method to the asymmetric synthesis

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