263382-27-0

Basic information

• Product Name: 1H-Pyrrole-2-carboxylicacid,5-(aminomethyl)-,methylester(9CI)
• Synonyms: 1H-Pyrrole-2-carboxylicacid,5-(aminomethyl)-,methylester(9CI);Methyl 5-(aMinoMethyl)-1H-pyrrole-2-carboxylate
• CAS NO: 263382-27-0
• Molecular Formula: C7H10N2O2
• Molecular Weight: 154.17
• Product Categories: GLYCINESCAFFOLD;CARBOXYLICESTER
• Mol File: 263382-27-0.mol

Chemical Properties

• Boiling Point: 316.391°C at 760 mmHg
• Flash Point: 145.148°C
• Appearance: /
• Density: 1.227g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.565
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 15.63±0.50(Predicted)
• CAS DataBase Reference: 1H-Pyrrole-2-carboxylicacid,5-(aminomethyl)-,methylester(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-2-carboxylicacid,5-(aminomethyl)-,methylester(9CI)(263382-27-0)
• EPA Substance Registry System: 1H-Pyrrole-2-carboxylicacid,5-(aminomethyl)-,methylester(9CI)(263382-27-0)

Safety Data

• Hazardous Substances Data: 263382-27-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1H-Pyrrole-2-carboxylic acid, 5-(aminomethyl)-, methyl ester (9CI) is used as a building block for the synthesis of various drugs. Its unique structure allows for the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agricultural Industry:
In the agricultural sector, 1H-Pyrrole-2-carboxylic acid, 5-(aminomethyl)-, methyl ester (9CI) serves as a precursor for the synthesis of agrochemicals. Its properties make it a valuable component in the creation of effective and targeted pesticides or other agricultural products.
Used in Medicinal Research:
1H-Pyrrole-2-carboxylic acid, 5-(aminomethyl)-, methyl ester (9CI) is studied for its potential medicinal properties, including anti-inflammatory and anti-cancer effects. Its unique chemical structure may contribute to the development of new treatments for various diseases and conditions.
Used in Material Science:
1H-Pyrrole-2-carboxylicacid,5-(aminomethyl)-,methylester(9CI) may also have applications in the development of new materials and organic compounds. Its versatile chemical structure allows for potential use in creating innovative materials with unique properties for various industries.

InChI:InChI=1/C7H10N2O2/c1-11-7(10)6-3-2-5(4-8)9-6/h2-3,9H,4,8H2,1H3

Upstream product

• 1197-13-3 methyl 5-formyl-1H-pyrrole-2-carboxylate 
• 35302-72-8 pyrrol-2-yl trichloromethyl ketone 
• 1193-62-0 methyl Pyrrole-2-carboxylate 
• 1003-29-8 2-pyrrole aldehyde 
• 442537-64-6 5-azidomethyl-1H-pyrrole-2-carboxylic acid methyl ester 
• 263382-26-9 Methyl 5-[(hydroxyimino)methyl]-1H-pyrrole-2-carboxylate 

Relevant articles and documents

Naphthalene and pyrrole substituted guanidine in selective sensing of Cu2+, Hg2+, Pb2+ and CN? ions under different conditions

Naphthalene and pyrrole substituted guanidine 1 has been designed and synthesised. Compound 1 efficiently distinguishes Cu2+, Hg2+ and Pb2+ ions by exhibiting different responses in fluorescence. While compound 1 exhibited turn-on emission selectively in the presence of Hg2+ and Pb2+ ions in CH3CN and CH3CN–H2O (1:1, v/v), respectively, it showed decrease in emission upon interaction with Cu2+ ion in CH3CN. Furthermore, the Cu-1 ensemble has been established as a potential probe for selective detection of CN? ion over a series of other anions involving colour change (in ordinary light: colourless to light yellow and under UV light: colourless to sky blue). Theoretical insight has been invoked to understand the mode of metal–ligand interaction.

Development of 5-(aminomethyl)pyrrole-2-carboxylic acid as a constrained surrogate of Gly-ΔAla and its application in peptidomimetic studies

A new peptidomimetic scaffold based on 5-(aminomethyl)pyrrole-2-carboxylic acid (1) is developed for the first time and used as a conformationally constrained surrogate of the Gly-ΔAla dipeptide isostere (2) to prepare peptides 3 and 4.

Carboxylate Binding by 2-(Guanidiniocarbonyl)pyrrole Receptors in Aqueous Solvents: Improving the Binding Properties of Guanidinium Cations through Additional Hydrogen Bonds

A series of guanidiniocarbonyl pyrrole receptors has been synthesized which bind carboxylates by ion pairing in combination with multiple hydrogen bonds. Their binding properties with various carboxylates have been investigated using NMR titration studies in 40% water/DMSO (ν/ν). The best receptor has association constants which are in the order of K ≈ 103 mol-1 and hence some 30 times larger than with the simple acetyl guanidinium cation. Through a systematic variation of the receptor structure, semiquantitative estimates for the energetic contributions of the individual binding interactions could be derived. These data show that the various hydrogen bonds are not equally important for the binding but differ significantly in their energetic contribution to the overall complexation process. Furthermore, the receptor can be made chiral and shows selectivity upon binding of enantiomeric amino acid carboxylates. Molecular modeling was used to obtain structural information for the various receptor carboxylate complexes and served as a basis to explain the observed differences in binding constants.