5555-70-4

Basic information

• Product Name: N-(4-Chlor-benzyloxy)-carbaminsaeure-ethylester
• CAS NO: 5555-70-4
• Molecular Weight: 229.663
• Mol File: 5555-70-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(4-Chlor-benzyloxy)-carbaminsaeure-ethylester(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-Chlor-benzyloxy)-carbaminsaeure-ethylester(5555-70-4)
• EPA Substance Registry System: N-(4-Chlor-benzyloxy)-carbaminsaeure-ethylester(5555-70-4)

Safety Data

• Hazardous Substances Data: 5555-70-4(Hazardous Substances Data)

Upstream product

• 589-41-3 ethyl N-hydroxylcarbamate 
• 104-83-6 1-Chloro-4-(chloromethyl)benzene 
• 622-95-7 4-chlorobenzyl bromide 

Downstream Products

• 38936-60-6 O-(4-chlorobenzyl)hydroxylamine hydrochloride 
• 107682-57-5 N-(2,5-Dichlor-phenyl)-N'-(4-chlor-benzyloxy)-harnstoff 
• 106421-91-4 N-<4-Chlor-phenyl>-N'-<4-chlor-benzyloxy>-harnstoff 
• 100716-37-8 N-Phenyl-N'-<4-chlor-benzyloxy>-thioharnstoff 
• 107058-42-4 N-<4-Chlor-benzyl>-N'-<4-chlor-benzyloxy>-thioharnstoff 
• 101103-30-4 N,N'-Bis-(4-chlor-benzyloxy)-harnstoff 
• 102020-67-7 N-Undecyl-N'-(4-chlor-benzyloxy)-harnstoff 
• 101887-61-0 N-Dec-9-enyl-N'-(4-chlor-benzyloxy)-harnstoff 
• 30204-37-6 C₁₀H₁₁ClN₂O₄ 
• 106320-04-1 4-chloro-benzaldehyde-[O-(4-chloro-benzyl)-oxime ] 
• 5555-51-1 (4-chlorobenzyl)oxyamine 
• 30204-29-6 (4-chloro-benzyloxy)-urea 

Relevant articles and documents

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

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.