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204139-61-7

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204139-61-7 Usage

General Description

4-(1-CBZ-PIPERIDIN-4-YL)-BUTYRIC ACID is a chemical compound that contains a piperidine ring, a butyric acid moiety, and a carbobenzyloxy protecting group. It is often used in the synthesis of pharmaceuticals and as a building block for drug discovery. The piperidine ring is a common structural motif in many drugs and natural products, and the butyric acid moiety contributes to the compound's solubility and bioavailability. The carbobenzyloxy protecting group is used to protect reactive functional groups during chemical reactions, allowing for selective manipulation of the compound's structure. Overall, 4-(1-CBZ-PIPERIDIN-4-YL)-BUTYRIC ACID is a versatile compound with potential applications in drug development and chemical synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 204139-61-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,1,3 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 204139-61:
(8*2)+(7*0)+(6*4)+(5*1)+(4*3)+(3*9)+(2*6)+(1*1)=97
97 % 10 = 7
So 204139-61-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H23NO4/c19-16(20)8-4-7-14-9-11-18(12-10-14)17(21)22-13-15-5-2-1-3-6-15/h1-3,5-6,14H,4,7-13H2,(H,19,20)

204139-61-7SDS

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 4-(1-phenylmethoxycarbonylpiperidin-4-yl)butanoic 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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:204139-61-7 SDS

204139-61-7Downstream Products

204139-61-7Relevant articles and documents

Enantioselective α-arylation of N-acyloxazolidinones with copper(II)-bisoxazoline catalysts and diaryliodonium salts

Bigot, Aurelien,Williamson, Alice E.,Gaunt, Matthew J.

supporting information; experimental part, p. 13778 - 13781 (2011/10/09)

A new strategy for the catalytic enantioselective α-arylation of N-acyloxazolidinones with chiral copper(II)-bisoxazoline complexes and diaryliodonium salts is described. The mild catalytic conditions are operationally simple, produce valuable synthetic building blocks in excellent yields and enantioselectivities, and can be applied to the synthesis of important nonsteroidal anti-inflammatory agents and their analogues.

Process for the preparation of azacycloalkylakanoyl pseudotetrapeptides

-

, (2008/06/13)

This invention is directed to a process for preparing a pseudotetrapeptide of formula I or a salt or prodrug thereof wherein is optionally nitrogen protected azaheterocyclyl; is a single or double bond; q is 1-5; B is alkyl, cycloalkyl, cycloalkylalkyl, alkylcycloalkyl, alkylcycloalkylalkyl, aryl, aralkyl, alkylaryl, or alkylaralkyl; Q2 is H or a carboxylic acid protecting group; J is —H, alkyl, cycloalkyl, cycloalkylalkyl, alkylcycloalkyl, alkylcycloalkylalkyl, aryl, substituted aryl, aralkyl, substituted aralkyl; L is OR1, or NR1R2, where R1 and R2 are independently —H, alkyl, cycloalkyl, cycloalkylalkyl, alkylcycloalkyl, alkylcycloalkylalkyl, aryl, aralkyl, alkylaryl or alkylaralkyl; and p is 1 or 2 which comprises the coupling of two dipeptides or psuedopeptides.

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