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5-PHENYL-PIPERIDINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER is a heterocyclic organic compound derived from piperidine, featuring a phenyl group attached to the piperidine ring and two carboxylic acid groups at the 1 and 3 positions. The tert-butyl ester functional group enhances its stability, making it a versatile building block in the synthesis of pharmaceutical drugs and bioactive compounds. Its molecular structure and properties render it a promising candidate for developing new drugs to target a range of diseases, including cancer, neurological disorders, and infectious diseases.

885274-99-7

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885274-99-7 Usage

Uses

Used in Medicinal Chemistry:
5-PHENYL-PIPERIDINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER is used as a building block for the synthesis of various pharmaceutical drugs and bioactive compounds due to its stable and versatile molecular structure.
Used in Drug Discovery:
In the field of drug discovery, 5-PHENYL-PIPERIDINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER is utilized as a potential candidate for the development of new drugs targeting diseases such as cancer, neurological disorders, and infectious diseases, owing to its unique molecular properties and structure.
Used in Pharmaceutical Industry:
5-PHENYL-PIPERIDINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER is used as a key intermediate in the synthesis of complex drug molecules, contributing to the advancement of novel therapeutic agents for the treatment of various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 885274-99-7 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 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 885274-99:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*4)+(2*9)+(1*9)=227
227 % 10 = 7
So 885274-99-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H23NO4/c1-17(2,3)22-16(21)18-10-13(9-14(11-18)15(19)20)12-7-5-4-6-8-12/h4-8,13-14H,9-11H2,1-3H3,(H,19,20)

885274-99-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(2-methylpropan-2-yl)oxycarbonyl]-5-phenylpiperidine-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 5-Phenyl-piperidine-1,3-dicarboxylic acid 1-tert-butyl ester

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:885274-99-7 SDS

885274-99-7Relevant academic research and scientific papers

CASPASE 6 INHIBITORS AND USES THEREOF

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, (2021/05/29)

Disclosed herein, inter alia, are compounds and methods for inhibiting Caspase 6 and the treatment of diseases. Provided is a method of treating a neurodegenerative disease, the method including administering to a subject in need thereof an effective amou

LOX ENZYME INHIBITING METHODS AND COMPOSITIONS

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, (2021/10/30)

This invention relates to compounds, pharmaceutical compositions and their use for treating fibrotic disorders, proliferative disorders, cardiovascular diseases, acute and chronic inflammatory disorders, primary and metastatic cancer, pulmonary conditions, ocular diseases, or neurological and neuropsychiatric conditions. One particular aspect of the inventions relates to inhibitors of the family of lysyl oxidase enzymes and their use as therapeutics for fibrotic disorders.

1,5-Substituted nipecotic amides: Selective PDE8 inhibitors displaying diastereomer-dependent microsomal stability

DeNinno, Michael P.,Wright, Stephen W.,Visser, Michael S.,Etienne, John B.,Moore, Dianna E.,Olson, Thanh V.,Rocke, Benjamin N.,Andrews, Melissa P.,Zarbo, Cynthia,Millham, Michele L.,Boscoe, Brian P.,Boyer, David D.,Doran, Shawn D.,Houseknecht, Karen L.

, p. 3095 - 3098 (2011/06/24)

The first highly potent and selective PDE8 inhibitors are disclosed. The initial tetrahydroisoquinoline hit was transformed into a nipecotic amide series in order to address a reactive metabolite issue. Reduction of lipophilicity to address metabolic liab

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