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496841-07-7

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496841-07-7 Usage

Description

(2S,3R)-N-tert-Butoxycarbonyl-3-benzoyloxy-2-pyrrolidinecarboxylic acid methyl ester is a complex organic compound that features a pyrrolidine ring and multiple functional groups. It is an ester derivative of pyrrolidinecarboxylic acid, with the presence of tert-butoxycarbonyl and benzoyloxy substituents. (2S,3R)-N-tert-Butoxycarbonyl-3-benzoyloxy-2-pyrrolidinecarboxylic acid methyl ester is classified within the peptide group of organic compounds and is frequently utilized in the realms of chemical synthesis and pharmaceutical research. Its distinct stereochemistry and functional groups render it a valuable asset in the creation of novel drugs and biologically active molecules. (2S,3R)-N-tert-Butoxycarbonyl-3-benzoyloxy-2-pyrrolidinecarboxylic acid methyl ester's unique attributes and potential applications have positioned it as a significant focus for both organic and medicinal chemists.

Uses

Used in Pharmaceutical Research:
(2S,3R)-N-tert-Butoxycarbonyl-3-benzoyloxy-2-pyrrolidinecarboxylic acid methyl ester is employed as a key intermediate in the synthesis of pharmaceuticals, particularly for the development of new drugs and biologically active compounds. Its unique stereochemistry and functional groups contribute to its potential as a building block in medicinal chemistry.
Used in Chemical Synthesis:
In the field of chemical synthesis, (2S,3R)-N-tert-Butoxycarbonyl-3-benzoyloxy-2-pyrrolidinecarboxylic acid methyl ester is used as a versatile reagent for the creation of a variety of complex organic molecules. Its functional groups allow for multiple synthetic pathways, making it a valuable component in the synthesis of diverse chemical libraries.
Used in Drug Development:
(2S,3R)-N-tert-Butoxycarbonyl-3-benzoyloxy-2-pyrrolidinecarboxylic acid methyl ester is utilized in drug development as a precursor for the synthesis of potential therapeutic agents. Its specific structural features can be tailored to target specific biological pathways, offering a promising avenue for the creation of new treatments for various diseases.
Used in Organic Chemistry Research:
In the realm of organic chemistry research, (2S,3R)-N-tert-Butoxycarbonyl-3-benzoyloxy-2-pyrrolidinecarboxylic acid methyl ester serves as a model compound for studying reaction mechanisms and exploring new synthetic methodologies. Its complex structure and functional groups provide a rich platform for understanding and advancing the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 496841-07-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,6,8,4 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 496841-07:
(8*4)+(7*9)+(6*6)+(5*8)+(4*4)+(3*1)+(2*0)+(1*7)=197
197 % 10 = 7
So 496841-07-7 is a valid CAS Registry Number.

496841-07-7SDS

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 2-Methyl 1-(2-methyl-2-propanyl) (2S,3R)-3-(benzoyloxy)-1,2-pyrro lidinedicarboxylate

1.2 Other means of identification

Product number -
Other names (2S,3R)-N-tert-butyloxycarbonyl-3-benzoyloxy-2-pyrrolidine carboxylic acid methyl 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:496841-07-7 SDS

496841-07-7Relevant articles and documents

Discovery of potent and muscle selective androgen receptor modulators through scaffold modifications

Li, James J.,Sutton, James C.,Nirschl, Alexandra,Zou, Yan,Wang, Haixia,Sun, Chongqing,Pi, Zulan,Johnson, Rebecca,Krystek Jr., Stanley R.,Seethala, Ramakrishna,Golla, Rajasree,Sleph, Paul G.,Beehler, Blake C.,Grover, Gary J.,Fura, Aberra,Vyas, Viral P.,Li, Cindy Y.,Gougoutas, Jack Z.,Galella, Michael A.,Zahler, Robert,Ostrowski, Jacek,Hamann, Lawrence G.

, p. 3015 - 3025 (2008/02/06)

A novel series of imidazolin-2-ones were designed and synthesized as highly potent, orally active and muscle selective androgen receptor modulators (SARMs), with most of the compounds exhibiting low nM in vitro potency in androgen receptor (AR) binding and functional assays. Once daily oral treatment with the lead compound 11a (AR Ki = 0.9 nM, EC50 = 1.8 nM) for 14 days induced muscle growth with an ED50 of 0.09 mg/kg, providing approximately 50-fold selectivity over prostate growth in an orchidectomized rat model. Pharmacokinetic studies in rats demonstrated that the lead compound 11a had oral bioavailability of 65% and a plasma half-life of 5.5 h. On the basis of their preclinical profiles, the SARMs in this series are expected to provide beneficial anabolic effects on muscle with minimal androgenic effects on prostate tissue.

Bicyclic modulators of androgen receptor function

-

, (2008/06/13)

The invention provides for a pharmaceutical composition capable of modulating the androgen receptor comprising a compound of formula I wherein the substitutents are as described herein. Further provided are methods of using such compounds for the treatment of nuclear hormone receptor-associated conditions, such as age related diseases, for example sarcopenia. Also provided are pharmaceutical compositions containing such compounds and processes for preparing some of the compounds of the invention.

Bicyclic modulators of androgen receptor function

-

, (2008/06/13)

The invention provides compounds of the formula I wherein the substitutents are as described herein. Further provided are methods of using such compounds for the treatment of nuclear hormone receptor-associated conditions, such as age related diseases, for example sarcopenia, and also provided are pharmaceutical compositions containing such compounds.

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