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The chemical compound "quinolin-8-yl ester of N-benzyloxycarbonyl-L-phenylalanine" is a complex organic molecule with a molecular formula of C28H24N2O4. It is derived from the amino acid L-phenylalanine, which is an essential amino acid for humans. In quinolin-8-yl ester of N-benzyloxycarbonyl-L-phenylalanine, L-phenylalanine is modified with a protective group, the N-benzyloxycarbonyl (N-Z) group, which is commonly used in peptide synthesis to prevent unwanted side reactions. The quinolin-8-yl ester group is attached to the carboxylic acid group of the phenylalanine, providing a quinoline-based functionality. This specific chemical structure may be of interest in medicinal chemistry, particularly in the design of new drugs or as a building block for more complex molecules. The compound's properties, such as solubility and reactivity, can be influenced by the presence of these functional groups, making it a potentially valuable intermediate in the synthesis of pharmaceuticals or other bioactive compounds.

2440-94-0

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2440-94-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2440-94-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,4 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2440-94:
(6*2)+(5*4)+(4*4)+(3*0)+(2*9)+(1*4)=70
70 % 10 = 0
So 2440-94-0 is a valid CAS Registry Number.

2440-94-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name quinolin-8-yl ester of N-benzyloxycarbonyl-L-phenylalanine

1.2 Other means of identification

Product number -
Other names Z-L-Phe-O-Qu

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:2440-94-0 SDS

2440-94-0Relevant articles and documents

ACTIVATION OF A CARBOXY GROUP BY DIALKYL PYROCARBONATES. SYNTHESIS OF SYMMETRICAL ANHYDRIDES AND ARYL ESTERS OF N-PROTECTED AMINO ACIDS USING DI-tert-BUTYL PYROCARBONATE AS CONDENSING REAGENT

Pozdnev, V. F.,Chernaya, M. Yu.

, p. 333 - 337 (2007/10/02)

It has been shown that di-tert-butyl pyrocarbonate can be used as a condensing reagent in the production of anhydrides and some aryl esters of carboxylic acids.The synthesis of anhydrides and of phenyl, p-nitrophenyl, β-naphtyl, and quinolin-8-yl esters of N-protected amino acids is described.

Process for the preparation of a carboxylic acid ester

-

, (2008/06/13)

An improved and novel process for the preparation of a carboxylic acid ester which comprises reacting a carboxylic acid with an alcohol or a sulfenic acid ester thereof in the presence of a tertiary phosphine and a disulfide of a mercaptoheterocyclic compound containing a nitrogen-carbon double bond with which the disulfide linkage is conjugated.

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