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2-Methylimidazo[1,2-a]pyridin-3-amine is a heterocyclic organic compound characterized by its unique fused-ring structure that includes both imidazole and pyridine rings. With the molecular formula C8H8N4, 2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE is found in various pharmaceutical drugs and is known for its distinctive chemical and biological properties. Its potential applications in treating a range of diseases, such as cancer and neurological disorders, are currently under active investigation in the fields of medicinal chemistry and drug development.

28036-31-9

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28036-31-9 Usage

Uses

Used in Pharmaceutical Development:
2-Methylimidazo[1,2-a]pyridin-3-amine is utilized as a key component in the development of pharmaceutical drugs due to its unique chemical structure and potential therapeutic effects. Its presence in drug formulations is attributed to its ability to interact with specific biological targets, which may contribute to the treatment of various diseases.
Used in Cancer Treatment Research:
In the field of oncology, 2-Methylimidazo[1,2-a]pyridin-3-amine is studied for its potential as an anticancer agent. 2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE's interactions with cellular and molecular targets are of particular interest, as they may provide insights into the development of novel cancer therapies.
Used in Neurological Disorder Research:
2-Methylimidazo[1,2-a]pyridin-3-amine is also being investigated for its possible role in the treatment of neurological disorders. Its unique properties may offer new avenues for understanding and managing such conditions, making it a valuable subject of research in neurochemistry and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 28036-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,3 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28036-31:
(7*2)+(6*8)+(5*0)+(4*3)+(3*6)+(2*3)+(1*1)=99
99 % 10 = 9
So 28036-31-9 is a valid CAS Registry Number.

28036-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE

1.2 Other means of identification

Product number -
Other names 2-methyl-imidazo[1,2-a]pyridin-3-amine

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:28036-31-9 SDS

28036-31-9Relevant academic research and scientific papers

3-Benzamido, ureido and thioureidoimidazo[1,2-a]pyridine derivatives as potential antiviral agents

Chaouni-Benabdallah, Aziz,Galtier, Christophe,Allouchi, Hassan,Kherbeche, Abdelak,Chavignon, Olivier,Teulade, Jean-Claude,Witvrouw, Myriam,Pannecouque, Christophe,Snoeck, Robert,Andrei, Graciela,Balzarini, Jan,De Clercq, Erik,Fauvelle, Florence,Enguehard, Cecile,Gueiffier, Alain

, p. 1631 - 1635 (2001)

This work reports the synthesis and the antiviral activities of 3-benzamido, 3-phenylureido and 3-phenylthioureido derivatives in the imidazo[1,2-a]pyridine series. The structure was proven by NMR spectroscopy. The synthesized compounds were evaluated against a large number of viruses. The 3-phenylthioureido derivative 7 showed moderate activity against human cytomegalovirus (HCMV) in vitro. The crystallographic data for 8 are also reported and explain the absence of activity against human immunodeficiency virus (HIV).

New pyrazole derivatives as CRAC channel modulators

-

, (2015/03/28)

The present invention relates to compounds of formula (I) which are inhibitors of CRAC channel activity. This invention also relates to pharmaceutical compositions containing them, process for their preparation and their use in therapy.

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