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(S)-2-(2-Nitrobenzyl)pyrrolidine-2-carboxylic acid hydrochloride is a chemical compound with the molecular formula C15H18N2O4Cl. It is a hydrochloride salt form of the compound, which consists of a pyrrolidine ring with a carboxylic acid and nitrobenzyl group attached to it. This chemical is commonly used in pharmaceutical research and development as a building block for the synthesis of various drug molecules. It is also used as a chiral building block in the preparation of diverse pharmaceutical compounds. The hydrochloride salt form of (S)-2-(2-Nitrobenzyl)pyrrolidine-2-carboxylic acid increases its solubility in water and makes it easier to handle in laboratory settings. (S)-2-(2-Nitrobenzyl)pyrrolidine-2-carboxylic acid hydrochloride is important for the synthesis of new drugs and pharmaceutical compounds.

1049742-66-6

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1049742-66-6 Usage

Uses

Used in Pharmaceutical Research and Development:
(S)-2-(2-Nitrobenzyl)pyrrolidine-2-carboxylic acid hydrochloride is used as a building block for the synthesis of various drug molecules. Its unique structure and functional groups make it a valuable component in the development of new pharmaceutical compounds.
Used in Chiral Building Blocks:
(S)-2-(2-Nitrobenzyl)pyrrolidine-2-carboxylic acid hydrochloride is used as a chiral building block in the preparation of diverse pharmaceutical compounds. Its specific stereochemistry allows for the creation of enantiomerically pure compounds, which is crucial for the development of effective and safe drugs.
Used in Laboratory Settings:
The hydrochloride salt form of (S)-2-(2-Nitrobenzyl)pyrrolidine-2-carboxylic acid increases its solubility in water, making it easier to handle in laboratory settings. This improved solubility facilitates its use in various chemical reactions and processes, contributing to the advancement of pharmaceutical research.
Used in Drug Synthesis:
(S)-2-(2-Nitrobenzyl)pyrrolidine-2-carboxylic acid hydrochloride is important for the synthesis of new drugs and pharmaceutical compounds. Its versatile structure and functional groups enable the development of innovative therapeutic agents with potential applications in various medical fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1049742-66-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,9,7,4 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1049742-66:
(9*1)+(8*0)+(7*4)+(6*9)+(5*7)+(4*4)+(3*2)+(2*6)+(1*6)=166
166 % 10 = 6
So 1049742-66-6 is a valid CAS Registry Number.

1049742-66-6Upstream product

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