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(3S,4R)-1-(tert-butoxycarbonyl)-4-phenylpiperidine-3-carboxylic acid is a chiral carboxylic acid derivative characterized by the presence of a piperidine ring and a phenyl group. It features a tert-butoxycarbonyl (Boc) protecting group on the nitrogen of the piperidine, which is crucial for its stability and reactivity in chemical reactions. (3S,4R)-1-(tert-butoxycarbonyl)-4-phenylpiperidine-3-carboxylic acid is known for its specific stereochemistry, denoted as (3S,4R), which is essential for its applications in various fields.

652971-20-5

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652971-20-5 Usage

Uses

Used in Organic Synthesis:
(3S,4R)-1-(tert-butoxycarbonyl)-4-phenylpiperidine-3-carboxylic acid is used as a building block in organic synthesis for its versatile reactivity and structural features. The presence of the Boc group allows for selective deprotection, enabling further functionalization of the molecule.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (3S,4R)-1-(tert-butoxycarbonyl)-4-phenylpiperidine-3-carboxylic acid is utilized as a key intermediate in the synthesis of various drugs. Its unique structure and chirality make it a valuable component in the development of new medicinal compounds with specific therapeutic targets.
Used in Agrochemical Development:
(3S,4R)-1-(tert-butoxycarbonyl)-4-phenylpiperidine-3-carboxylic acid is also employed in the agrochemical sector for the production of pesticides and other crop protection agents. Its structural properties allow for the creation of compounds with targeted biological activity against pests and diseases.
Used in Medicinal Chemistry and Drug Discovery:
In the field of medicinal chemistry, (3S,4R)-1-(tert-butoxycarbonyl)-4-phenylpiperidine-3-carboxylic acid serves as a valuable starting material for the design and synthesis of potential drug candidates. Its chiral nature and functional groups provide a foundation for the development of enantioselective reactions and the creation of novel bioactive molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 652971-20-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,2,9,7 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 652971-20:
(8*6)+(7*5)+(6*2)+(5*9)+(4*7)+(3*1)+(2*2)+(1*0)=175
175 % 10 = 5
So 652971-20-5 is a valid CAS Registry Number.

652971-20-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4R)-trans-N-(tert-butoxycarbonyl)-4-phenyl-3-carboxypiperidine

1.2 Other means of identification

Product number -
Other names (3S,4R)-1-(tert-Butoxycarbonyl)-4-phenylpiperidine-3-carboxylic acid

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:652971-20-5 SDS

652971-20-5Downstream Products

652971-20-5Relevant academic research and scientific papers

Design and syntheses of melanocortin subtype-4 receptor agonists: Evolution of the pyridazinone archetype

Ujjainwalla, Feroze,Warner, Daniel,Walsh, Thomas F.,Wyvratt, Matthew J.,Zhou, Changyou,Yang, Lihu,Kalyani, Rubana N.,MacNeil, Tanya,Van Der Ploeg, Lex H. T.,Rosenblum, Charles I.,Tang, Rui,Vongs, Aurawan,Weinberg, David H.,Goulet, Mark T.

, p. 4431 - 4435 (2007/10/03)

The discovery and optimization of a new class of non-peptidyl, pyridazinone derived melanocortin subtype-4 receptor agonists is disclosed.

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