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IMidazo[1,2-a]pyridine-3-carboxaldehyde, 5-aMinois a bicyclic heterocyclic chemical compound with the molecular formula C8H7N3O. It features an imidazo[1,2-a]pyridine ring with an aldehyde group at the 3rd position and an amino group at the 5th position. IMidazo[1,2-a]pyridine-3-carboxaldehyde, 5-aMinoserves as a versatile building block for the synthesis of pharmaceuticals and agrochemicals, and is valued for its potential in medicinal chemistry and drug discovery due to its ability to modulate biological targets.

35220-26-9

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35220-26-9 Usage

Uses

Used in Pharmaceutical Industry:
IMidazo[1,2-a]pyridine-3-carboxaldehyde, 5-aMinois used as a key intermediate in the synthesis of various pharmaceuticals for its potential to modulate biological targets. Its unique chemical structure allows for the development of new molecules with pharmacological activities, contributing to drug discovery and the creation of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, IMidazo[1,2-a]pyridine-3-carboxaldehyde, 5-aMinois utilized as a building block for the synthesis of agrochemicals. Its reactivity and chemical properties make it suitable for the development of new molecules with potential applications in crop protection and pest control, enhancing the efficiency and effectiveness of these products.
Used in Medicinal Chemistry Research:
IMidazo[1,2-a]pyridine-3-carboxaldehyde, 5-aMinois employed as a research tool in medicinal chemistry. Its ability to interact with biological targets makes it a valuable compound for studying the mechanisms of action of potential drugs and for the design of new therapeutic agents with improved efficacy and selectivity.
Used in Drug Discovery:
IMidazo[1,2-a]pyridine-3-carboxaldehyde, 5-aMinoplays a crucial role in drug discovery as a versatile intermediate. Its unique structure and reactivity enable the development of new molecules with potential pharmacological activities, aiding in the identification of novel drug candidates and the advancement of therapeutic treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 35220-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,2,2 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35220-26:
(7*3)+(6*5)+(5*2)+(4*2)+(3*0)+(2*2)+(1*6)=79
79 % 10 = 9
So 35220-26-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3O/c9-7-2-1-3-8-10-4-6(5-12)11(7)8/h1-5H,9H2

35220-26-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-aminoimidazo[1,2-a]pyridine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-Amino-3-formylimidazo<1,2-d>pyridin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:35220-26-9 SDS

35220-26-9Downstream Products

35220-26-9Relevant academic research and scientific papers

Synthetic method of imidazo[1,2-A]pyridine compounds

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Paragraph 0026-0038, (2021/08/21)

The invention belongs to the technical field of synthesis of drug intermediates, and particularly discloses a synthesis method of imidazo[1,2-A]pyridine compounds. According to the method disclosed by the invention, 2,6-diaminopyridine and 2-bromomalonaldehyde are adopted as raw materials and are subjected to one-step reaction under a simple heating reaction condition to obtain a target product. The method provided by the invention has the advantages of cheap and easily available raw materials, simple route, few reaction steps, convenient production, no need of using dangerous reducing reagents and heavy metal-containing oxidants, environmental protection, safety and easy purification.

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