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2-(S)-Methylpiperazine-1,4-dicarboxylic acid 4-benzyl ester 1-ter-butyl ester is a complex organic chemical compound characterized by a piperazine ring with two carboxylic acid groups and two ester groups, specifically a benzyl ester and a tert-butyl ester. 2-(S)-Methylpiperazine-1,4-dicarboxylic acid 4-benzyl ester 1-ter-butyl ester is distinguished by its stereochemistry at the methyl group, which is in the S-configuration. Piperazine derivatives, to which 2-(S)-Methylpiperazine-1,4-dicarboxylic acid 4-benzyl ester 1-ter-butyl ester belongs, are recognized for their diverse biological activities, making them valuable for pharmaceutical development.

859517-91-2

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859517-91-2 Usage

Uses

Used in Pharmaceutical Development:
2-(S)-Methylpiperazine-1,4-dicarboxylic acid 4-benzyl ester 1-ter-butyl ester is used as a precursor in the synthesis of pharmaceuticals due to its potential biological activities. The presence of the piperazine ring and the ester groups may contribute to its interaction with various biological targets, offering a wide range of therapeutic applications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2-(S)-Methylpiperazine-1,4-dicarboxylic acid 4-benzyl ester 1-ter-butyl ester serves as a valuable compound for studying structure-activity relationships. Its unique structure allows researchers to explore modifications that could enhance its pharmacological properties, such as improving solubility, bioavailability, and targeting specific receptors or enzymes.
Used in Drug Design:
2-(S)-Methylpiperazine-1,4-dicarboxylic acid 4-benzyl ester 1-ter-butyl ester is utilized in drug design for the development of new therapeutic agents. Its chemical structure can be optimized to target specific diseases, potentially leading to the creation of novel drugs with improved efficacy and safety profiles.
Used in the Synthesis of Bioactive Molecules:
2-(S)-Methylpiperazine-1,4-dicarboxylic acid 4-benzyl ester 1-ter-butyl ester is also used in the synthesis of other bioactive molecules, leveraging its unique structural features to create new compounds with potential applications in various therapeutic areas.
Used in the Development of Prodrugs:
Given its ester groups, 2-(S)-Methylpiperazine-1,4-dicarboxylic acid 4-benzyl ester 1-ter-butyl ester can be used in the development of prodrugs. Prodrugs are biologically inactive compounds that are metabolized in the body to produce an active drug, and the ester groups in 2-(S)-Methylpiperazine-1,4-dicarboxylic acid 4-benzyl ester 1-ter-butyl ester may facilitate such metabolic activation.

Check Digit Verification of cas no

The CAS Registry Mumber 859517-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,9,5,1 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 859517-91:
(8*8)+(7*5)+(6*9)+(5*5)+(4*1)+(3*7)+(2*9)+(1*1)=222
222 % 10 = 2
So 859517-91-2 is a valid CAS Registry Number.

859517-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-O-benzyl 1-O-tert-butyl (2S)-2-methylpiperazine-1,4-dicarboxylate

1.2 Other means of identification

Product number -
Other names (S)-4-benzyl 1-tert-butyl 2-methylpiperazine-1,4-dicarboxylate

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:859517-91-2 SDS

859517-91-2Relevant academic research and scientific papers

2-(AMINO-SUBSTITUTED)-4-ARYL PYRAMIDINES AND RELATED COMPOUNDS USEFUL FOR TREATING INFLAMMATORY DISEASES

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Page/Page column 134, (2008/06/13)

A heterocyclic inhibitor having the formula (I), with the variables defined herein, which is useful for treating inflammatory and other physiological disorders in which PKC-theta isoform plays a role.

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