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(R)-1-carboxy-3-methylbutyl 5-oxo-L-prolinate, a chemical compound with the molecular formula C11H17NO4, is a derivative of L-proline, an essential amino acid. (R)-1-carboxy-3-methylbutyl 5-oxo-L-prolinate is recognized for its unique stereochemistry and is widely utilized as a chiral building block in the realm of organic synthesis. Its structural properties allow it to serve as a versatile substrate for asymmetric catalysis, a technique crucial for creating enantiomerically pure compounds that are essential in various applications.

37755-50-3

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37755-50-3 Usage

Uses

Used in Pharmaceutical Production:
(R)-1-carboxy-3-methylbutyl 5-oxo-L-prolinate is employed as a key intermediate in the synthesis of pharmaceuticals. Its role in creating enantiomerically pure compounds is vital, as the purity of a drug's enantiomers can significantly impact its efficacy and safety profile. (R)-1-carboxy-3-methylbutyl 5-oxo-L-prolinate contributes to the development of life-saving medications and therapeutic agents.
Used in Agrochemical Synthesis:
In the agrochemical industry, (R)-1-carboxy-3-methylbutyl 5-oxo-L-prolinate is used as a chiral building block for the production of various agrochemicals. Its application in this field aids in the development of more effective and environmentally friendly pesticides, herbicides, and other agricultural products.
Used as a Chiral Ligand in Asymmetric Catalysis:
(R)-1-carboxy-3-methylbutyl 5-oxo-L-prolinate is also utilized as a chiral ligand in asymmetric catalysis. This application is significant in the synthesis of biologically active molecules, as it allows for the creation of compounds with specific stereochemistry, which can be crucial for their biological activity and selectivity.
Used in the Synthesis of Biologically Active Molecules:
(R)-1-carboxy-3-methylbutyl 5-oxo-L-prolinate is a valuable tool in the synthesis of biologically active molecules due to its unique stereochemistry. It is used to produce molecules with specific spatial arrangements that are essential for their interaction with biological targets, such as receptors or enzymes, leading to potential applications in drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 37755-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,5 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37755-50:
(7*3)+(6*7)+(5*7)+(4*5)+(3*5)+(2*5)+(1*0)=143
143 % 10 = 3
So 37755-50-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO5/c1-6(2)5-8(10(14)15)17-11(16)7-3-4-9(13)12-7/h6-8H,3-5H2,1-2H3,(H,12,13)(H,14,15)/t7-,8+/m0/s1

37755-50-3SDS

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)-4-methyl-2-[(2S)-5-oxopyrrolidine-2-carbonyl]oxypentanoic acid

1.2 Other means of identification

Product number -
Other names EINECS 253-654-6

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:37755-50-3 SDS

37755-50-3Upstream product

37755-50-3Downstream Products

37755-50-3Relevant academic research and scientific papers

Furan, benzofuran and tetrahydrofuran carboxylic acid esters

-

, (2008/06/13)

Compounds represented by the following formula EQU1 wherein A is a substituted or unsubstituted heterocyclic radical and T is a C2 -C5 alkyl, alkenyl, cyclopropylmethyl, cyclobutylmethyl or cyclopentyl group A process for their preparation and novel intermediates therefor are disclosed. These compounds are useful antibiotics.

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