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(3-BOC-AMINO-PYRROLIDIN-1-YL)-(1H-INDOL-2-YL)-ACETIC ACID is a heterocyclic compound that features an amino-pyrrolidine and an indole moiety connected to an acetic acid group. This structural composition is significant for its potential applications in medicinal chemistry and drug discovery. The presence of the "BOC" group indicates its utility as a protective group in organic synthesis, which is crucial for preventing unwanted reactions during the synthesis of biologically active molecules. (3-BOC-AMINO-PYRROLIDIN-1-YL)-(1H-INDOL-2-YL)-ACETIC ACID's specific biological activity and therapeutic potential are contingent upon its detailed structure and the intended target for interaction.
Used in Medicinal Chemistry:
(3-BOC-AMINO-PYRROLIDIN-1-YL)-(1H-INDOL-2-YL)-ACETIC ACID is used as a key intermediate in the synthesis of biologically active molecules for medicinal chemistry. Its unique structure allows for specific targeting of biological processes or protein interactions, which is essential for the development of new drugs.
Used in Drug Discovery:
In the field of drug discovery, (3-BOC-AMINO-PYRROLIDIN-1-YL)-(1H-INDOL-2-YL)-ACETIC ACID serves as a valuable compound for the design and optimization of new pharmaceutical agents. Its structural features facilitate its interaction with specific biological targets, making it a promising candidate for the treatment of various diseases.
Used in Organic Synthesis:
(3-BOC-AMINO-PYRROLIDIN-1-YL)-(1H-INDOL-2-YL)-ACETIC ACID is utilized as a protective group in organic synthesis to ensure that the desired chemical transformations occur without unwanted side reactions. This is particularly important in the preparation of complex biologically active molecules where selectivity and yield are critical factors.
Used in Chemical Research:
In chemical research, (3-BOC-AMINO-PYRROLIDIN-1-YL)-(1H-INDOL-2-YL)-ACETIC ACID is employed as a model compound to study the reactivity and properties of heterocyclic compounds. Understanding its behavior can provide insights into the development of new synthetic methods and the discovery of novel biologically active compounds.

885276-31-3

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885276-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 885276-31-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 885276-31:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*6)+(2*3)+(1*1)=213
213 % 10 = 3
So 885276-31-3 is a valid CAS Registry Number.

885276-31-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-amino-3-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidin-1-yl]-2-(1H-indol-2-yl)acetic acid

1.2 Other means of identification

Product number -
Other names -

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

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More Details:885276-31-3 SDS

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