59325-12-1

Basic information

• Product Name: 1-Piperazinecarboxylic acid, 4-(phenylmethyl)-, ethyl ester
• Synonyms: 1-Piperazinecarboxylic acid,4-(phenylmethyl)-,ethyl ester;1-(ethylcarboxy)-4-benzylpiperazine;1-Benzyl-4-carbethoxy-piperazin;ethyl 1-benzyl-4-carboxypiperazine;1-Benzyl-4-ethoxycarbonyl-piperazin;4-benzyl-piperazine-1-carboxylic acid ethyl ester;N-Aethoxycarbonyl-N'-benzyl-piperazin;4-Benzyl-piperazin-1-carbonsaeure-aethylester
• CAS NO: 59325-12-1
• Molecular Formula: C14H20N2O2
• Molecular Weight: 248.325
• Mol File: 59325-12-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-Piperazinecarboxylic acid, 4-(phenylmethyl)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Piperazinecarboxylic acid, 4-(phenylmethyl)-, ethyl ester(59325-12-1)
• EPA Substance Registry System: 1-Piperazinecarboxylic acid, 4-(phenylmethyl)-, ethyl ester(59325-12-1)

Safety Data

• Hazardous Substances Data: 59325-12-1(Hazardous Substances Data)

Upstream product

• 120-43-4 4-ethoxycarbonylpiperazine 
• 100-52-7 benzaldehyde 
• 100-44-7 benzyl chloride 
• 2759-28-6 1-phenylmethylpiperazine 
• 541-41-3 chloroformic acid ethyl ester 

Downstream Products

• 2759-28-6 1-phenylmethylpiperazine 
• 6935-82-6 4-benzylpiperazine-1-carbaldehyde 
• 749159-03-3 1-benzyl-4-<3-<(4-ethoxycoumarin-7-yl)oxy>propyl>piperazine 
• 75590-60-2 7-[3-(4-Benzyl-piperazin-1-yl)-propoxy]-4-hydroxy-chromen-2-one; hydrochloride 
• 75590-61-3 1-benzyl-4-[3-(4-hydroxy-3-nitrocoumarin-7-yloxy)propyl]piperazine 
• 23253-99-8 1-benzyl-4-(3-hydroxypropyl)piperazine 
• 165121-45-9 (4-benzyl-piperazin-1-yl)-acetyl chloride 
• 62226-74-8 1-benzyl-4-methylpiperazine 
• 120-43-4 4-ethoxycarbonylpiperazine 

Relevant articles and documents

Soluble polymer-supported catalysts containing azo dyes

(equation presented) Azo benzene derivatives were incorporated into soluble polymer-bound catalysts by two different approaches. The first was to attach the dye to the polymer-bound catalysts, using the dye as an innocent spectator to study the phase preference, concentration, and recoverability of a catalyst. The second approach used an azo dye as a ligand to form an effective soluble polymer-bound Pd(II) catalyst for Heck reactions.

Studies in Potential Filaricides: Part XV - Synthesis of 1-Acyl/Aryl-4-substituted-piperazines as Diethylcarbamazine Analogs

1-Acyl-4-substituted-piperazines (4-29) have been prepared starting from 1-benzylpiperazine while 1-aryl-4-aroylpiperazines (30-44) have been obtained from the corresponding 1-arylpiperazines.None of the compounds shows any significant filaricidal activity against Litomosoides carinii in cotton rats and cestodicial activity against Hymenolepis nana in mice.

A NOVEL SYNTHESIS OF PYRIDINECARBOXYLIC ACID PIPERAZIDES

N-Substituted piperazides of pyridinecarboxylic acids were synthesized in the following way: the pyridinecarboxylic acids were converted into (alkoxy-formic acid-pyridinecarboxylic acid) mixed anhydrides by means of alkyl chloroformates, and these were th