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N-(4-Chlor-benzyloxy)-carbaminsaeure-ethylester, also known as N-(4-chlorobenzyl)oxycarbonyl-L-aspartate ethyl ester, is a chemical compound with the molecular formula C12H14ClNO5. It is a derivative of aspartic acid, an amino acid, and is characterized by the presence of a 4-chlorobenzyl group attached to nitrogen the atom of the carbamoyl group, and an ethyl ester group on the carboxylic acid moiety. N-(4-Chlor-benzyloxy)-carbaminsaeure-ethylester is often used in organic synthesis and pharmaceutical chemistry, particularly in the synthesis of peptides and other biologically active molecules, due to its ability to protect the carblicoxy acid group during chemical reactions. The 4-chlorobenzyl group can be selectively removed under certain conditions, allowing for the controlled deprotection of the carboxylic acid function in the final product.

5555-70-4

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5555-70-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5555-70-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,5 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5555-70:
(6*5)+(5*5)+(4*5)+(3*5)+(2*7)+(1*0)=104
104 % 10 = 4
So 5555-70-4 is a valid CAS Registry Number.

5555-70-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-Chlor-benzyloxy)-carbamidsaeure-ethylester

1.2 Other means of identification

Product number -
Other names N-(4-Chlor-benzyloxy)-carbaminsaeure-ethylester

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

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More Details:5555-70-4 SDS

5555-70-4Relevant academic research and scientific papers

Synthesis and in vitro cytotoxic activity of N-2-(2-furyl)-2- (chlorobenzyloxyimino) ethyl ciprofloxacin derivatives

Alipour, Eskandar,Mohammadhosseini, Negar,Panah, Fatemeh,Ardestani, Sussan K.,Safavi, Maliheh,Shafiee, Abbas,Foroumadi, Alireza

scheme or table, p. 1226 - 1231 (2012/06/30)

Quinolone are a class of potent broad-spectrum antibacterial drugs that target the bacterial type II DNA topoisomerases (DNA gyrase) and topoisomerase IV. In the present study, the synthesis and evaluation of cytotoxicity activity of a new series of N-pipearzinyl quinolones containing N-2-(furyl-2-yl)-2- (chlorobenzyloxyimino) ethyl moiety (6a-c) have been studied. Preliminary screening showed that one of the new compounds, namely 7-(4-(2-(3- chlorobenzyloxyimino)-2-(furan-2-yl) ethyl) piperazin-1-yl)-1-cyclopropyl-6- fluoro-4-oxo-1, 4-dihydroquinoline-3-carboxylic acid (6b) showed significant cytotoxic activity against human breast tumor cell lines.

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