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(1R,4R)-4-(tert-butoxycarbonylamino)cyclopent-2-enecarboxylic acid, also known as t-Boc-cyclopent-2-ene-1,4-dicarboxylic acid, is a chemical compound with the molecular formula C12H17NO5. It is a derivative of cyclopent-2-ene-1,4-dicarboxylic acid, featuring a tert-butoxycarbonyl (t-Boc) protecting group attached to the amino group. (1R,4R)-4-(tert-butoxycarbonylamino)cyclopent-2-enecarboxylic acid plays a significant role in organic synthesis, particularly as a building block for the preparation of various compounds, such as pharmaceuticals and agrochemicals. The t-Boc protecting group enables selective reactions and can be removed under mild conditions, making it a valuable tool in synthetic chemistry. Additionally, (1R,4R)-4-(tert-butoxycarbonylamino)cyclopent-2-enecarboxylic acid is utilized in the development of novel drug candidates and research in medicinal chemistry.

298716-03-7

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298716-03-7 Usage

Uses

Used in Organic Synthesis:
(1R,4R)-4-(tert-butoxycarbonylamino)cyclopent-2-enecarboxylic acid is used as a building block in organic synthesis for the preparation of various compounds, including pharmaceuticals and agrochemicals. Its t-Boc protecting group allows for selective reactions, enhancing the versatility and efficiency of synthetic processes.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (1R,4R)-4-(tert-butoxycarbonylamino)cyclopent-2-enecarboxylic acid is used as a key intermediate in the synthesis of drug candidates. The t-Boc protecting group facilitates selective reactions, enabling the development of novel and effective pharmaceuticals with improved properties.
Used in Medicinal Chemistry Research:
(1R,4R)-4-(tert-butoxycarbonylamino)cyclopent-2-enecarboxylic acid is employed as a valuable tool in medicinal chemistry research. Its unique structure and the presence of the t-Boc protecting group make it suitable for exploring new chemical entities and understanding their interactions with biological targets, ultimately contributing to the advancement of drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 298716-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,8,7,1 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 298716-03:
(8*2)+(7*9)+(6*8)+(5*7)+(4*1)+(3*6)+(2*0)+(1*3)=187
187 % 10 = 7
So 298716-03-7 is a valid CAS Registry Number.

298716-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,4R)-4-(Boc-aMino)cyclopent-2-enecarboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Norbornyl oxime

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:298716-03-7 SDS

298716-03-7Relevant academic research and scientific papers

PRODUCTION OF TRANS-4-AMINOCYCLOPENT-2-ENE-1-CARBOXYLIC ACID DERIVATIVES

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, (2011/02/24)

Methods of producing compositions of trans-4-amino-2-cyclopentene-1-carboxylic acid derivatives are described. Also described is an amine salt of a compound having formula A, having components present in both cis and trans structures.

Process for the synthesis of E1 activating enzyme inhibitors

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Page/Page column 30, (2009/03/07)

The present invention provides processes and synthetic intermediates for the synthesis of 4-substituted ((1S,2S,4R)-2-hydroxy-4-{7H-pyrrolo[2,3-d]pyrimidin-7-yl}cyclopentyl)methyl sulfamates, which are E1 activating enzyme inhibitors, and are useful for t

Use of hydrolases for the synthesis of cyclic amino acids

Lloyd, Richard C.,Lloyd, Michael C.,Smith, Mark E. B.,Holt, Karen E.,Swift, Jonathan P.,Keene, Philip A.,Taylor, Stephen J. C.,McCague, Raymond

, p. 717 - 728 (2007/10/03)

The synthesis of several cyclic amino acids that have all the necessary structural features to make them ideal scaffolds for use in medicinal chemistry is described. A key step in each synthesis is the use of hydrolase enzymes to define a chiral centre. I

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