56903-89-0

Basic information

• Product Name: 2-Piperazinecarboxylicacid,4-methyl-,methylester(9CI)
• Synonyms: 2-Piperazinecarboxylicacid,4-methyl-,methylester(9CI);EETHYL 4-METHYLPIPERAZINE-2-CARBOXYLATE;methyl-4-methylpiperazine-2-carboxylate;4-Methyl-piperazine-2-carboxylic acid methyl ester;2-Piperazinecarboxylic acid, 4-methyl-, methyl ester
• CAS NO: 56903-89-0
• Molecular Formula: C7 H14 N2 O2
• Molecular Weight: 158.1983
• Product Categories: PIPERIDINE
• Mol File: 56903-89-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 216.8 °C at 760 mmHg
• Flash Point: 84.9 °C
• Appearance: /
• Density: 1.046 g/cm³
• Storage Temp.: Keep in dark place,Sealed in dry,Store in freezer, under -20°C
• CAS DataBase Reference: 2-Piperazinecarboxylicacid,4-methyl-,methylester(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Piperazinecarboxylicacid,4-methyl-,methylester(9CI)(56903-89-0)
• EPA Substance Registry System: 2-Piperazinecarboxylicacid,4-methyl-,methylester(9CI)(56903-89-0)

Safety Data

• Hazardous Substances Data: 56903-89-0(Hazardous Substances Data)

Usage

General Description

2-Piperazinecarboxylic acid, 4-methyl-, methylester (9CI) is a chemical compound that belongs to the class of piperazinecarboxylic acids. It is essentially the methyl ester form of 2-piperazinecarboxylic acid. 2-Piperazinecarboxylicacid,4-methyl-,methylester(9CI) is used in the pharmaceutical industry for various purposes, including as an intermediate in the synthesis of pharmaceutical drugs. It has potential applications in the treatment of various medical conditions and diseases. Additionally, it may also have uses in chemical and biochemical research. Overall, 2-Piperazinecarboxylic acid, 4-methyl-, methylester (9CI) is a versatile chemical with important potential applications in the pharmaceutical and research fields.

Upstream product

• 56903-88-9 1-benzyl-4-methyl-piperazine-2-carboxylic acid methyl ester 

Downstream Products

• 444163-58-0 4-methyl-1-(2-nitrobenzoyl)piperazine-2-carboxylic acid methyl ester 

Relevant articles and documents

Hybridized and isosteric analogues of N1-acetyl-N4-dimethyl-piperazinium iodide (ADMP) and N1-phenyl-N4-dimethyl-piperazinium iodide (DMPP) with central nicotinic action

A series of piperazine derivatives, obtained by hybridization of N1-acetyl-N4-dimethyl-piperazinium iodide (1, ADMP) and N1-phenyl-N4-dimethyl-piperazinium iodide (3, DMPP) or of the corresponding tertiary bases (2, 4) with arecoline (5) and arecolone (6) or by isosteric substitution of the phenyl ring of DMPP, has been synthesized. Hybridization afforded compounds that, both as tertiary bases and as iodomethylates, have no affinity for the nicotinic receptor. On the contrary, isosteric substitution gave compounds that maintain affinity for the receptor; among them, two tertiary bases (37, 38), show affinity in the nanomolar range for the nicotinic receptor. The pharmacological profile of these isomeric compounds is quite interesting as they present differences in their peripheral and central effects, suggesting that they interact with different subtypes of the nicotinic receptor. Copyright (C) 1999 Elsevier Science Ltd.