126202-06-0

Basic information

• Product Name: 1(2H)-Pyridineaceticacid,2-imino-(9CI)
• Synonyms: 1(2H)-Pyridineaceticacid,2-imino-(9CI);2-(2-Iminopyridin-1(2H)-yl)acetic acid
• CAS NO: 126202-06-0
• Molecular Formula: C₇H₈N₂O₂
• Molecular Weight: 152.152
• Product Categories: GLYCINESCAFFOLD
• Mol File: 126202-06-0.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 308.0±44.0 °C(Predicted)
• Appearance: /
• Density: 1.28±0.1 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 2.78±0.10(Predicted)
• CAS DataBase Reference: 1(2H)-Pyridineaceticacid,2-imino-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1(2H)-Pyridineaceticacid,2-imino-(9CI)(126202-06-0)
• EPA Substance Registry System: 1(2H)-Pyridineaceticacid,2-imino-(9CI)(126202-06-0)

Safety Data

• Hazardous Substances Data: 126202-06-0(Hazardous Substances Data)

Usage

Description

1(2H)-Pyridineacetic acid, 2-imino-(9CI), also known as 2-(2-Iminopyridin-1(2H)-yl)acetic acid, is an organic compound with the molecular formula C6H6N2O2. It is a derivative of pyridineacetic acid and features an imino group at the 2nd position. 1(2H)-Pyridineaceticacid,2-imino-(9CI) serves as a key intermediate in the synthesis of various organic compounds, particularly those with potential applications in the pharmaceutical and chemical industries.

Uses

Used in Pharmaceutical Industry:
1(2H)-Pyridineacetic acid, 2-imino-(9CI) is used as a key intermediate in the synthesis of organoselenium imidazo[1,2-a]pyridine compounds. These compounds have been studied for their antimicrobial properties, making them potentially valuable in the development of new antibiotics and antifungal agents to combat drug-resistant infections.
Used in Chemical Industry:
In the chemical industry, 1(2H)-Pyridineacetic acid, 2-imino-(9CI) can be utilized as a building block for the creation of various complex organic molecules with diverse applications. Its unique structure allows for further functionalization and modification, enabling the development of new compounds with specific properties and reactivity.

Upstream product

• 504-29-0 2-aminopyridine 
• 79-11-8 chloroacetic acid 
• 7748-25-6 potassium chloroacetate 
• 3926-62-3 sodium monochloroacetic acid 

Downstream Products

• 3999-05-1 2-chloroimidazo[1,2-a]pyridine 
• 131773-23-4 2-chloroimidazo[1,2-a]pyridine-3-carbaldehyde 
• 956077-87-5 2-(4-methoxyphenyl)-3-nitroimidazo[1,2-a]pyridine 
• 67292-98-2 3-nitro-2-phenylimidazo<1,2-a>pyridine 
• 82193-32-6 3-amino-2-cyanoimidazo[1,2-a]pyridine 
• 1452807-24-7 C₁₃H₁₀N₄O₂ 
• 1452807-23-6 2-phenyl-N-(pyridin-3-yl)imidazo[1,2-a]pyridin-3-amine 
• 1452807-22-5 N-(4-chlorophenyl)-2-phenylimidazo[1,2-a]pyridin-3-amine 

Relevant articles and documents

Synthesis and Structure of 2-(1Н-Indol-1-yl)-6-ferrocenyl-4-(2-chloroimidazo[1,2-a]pyridin-3-yl)pyrimidine

A 2,4,6-trisubstituted pyrimidine including a 2-(1H-indol-1-yl) substituent was synthesized by the reaction of 1-ferrocenyl-3-(2-chloroimidazo[1,2-a]pyridin-3-yl)propanone with 2,5-dimethoxytetrahydrofuran. The structure of the synthesized compound was confirmed by IR and 1Н NMR spectroscopy, and X-ray diffraction analysis. It has been shown that the ferrocene-containing compounds synthesized in the present work all demonstrate intramolecular charge transfer which is evidenced by the observation of the corresponding absorption bands with λmaxabs > 480 nm. The oxidation potential of ferrocene (EoxFc) in all the compounds is higher than 700 mV.

Facile synthesis, structural evaluation, antimicrobial activity and synergistic effects of novel imidazo[1,2-a]pyridine based organoselenium compounds

A simple and efficient method has been described to synthesize the hitherto unknown imidazo[1,2-a]pyridine selenides (5a-l) by reaction of 2-chloroimidazo [1,2-a]pyridines with aryl/heteroaryl selenols, generated in situ by reduction of various diselenide

Synthesis and Physicochemical Properties of New Chalcones Containing a 2-Chloroimidazo[1,2-a]pyridine Fragment

Abstract: New chalcones containing a 2-chloroimidazo[1,2-a]pyridine fragment have been synthesized, and their optical properties have been studied. The Stokes shifts, forbidden band gap widths, molar absorption coefficients, and fluorescence quantum yields have been determined on the basis of their absorption and emission spectra. Introduction of an additional thiophene fragment into the chalcone molecules produced an increase of the Stokes shift, red shift of the emission maximum, and sharp increase of the quantum yield (up to 22%). The synthesized chalcones showed high thermal stability and good film-forming properties, and films obtained therefrom exhibited an ordered structure.

FUSED HETEROCYCLIC COMPOUNDS AND THEIR USE AS PEST CONTROL AGENTS

The present invention discloses a fused heterocyclic compound of formula (I), wherein, R1, Y, Q, A, G,m and E are as defined in the detailed description. The present invention further discloses methods for their preparation and use of the compounds of formula (I) as a pest control agent.