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(5-METHYLIMIDAZO[1,2-A]PYRIDIN-3-YL)METHANOL is a chemical compound with the molecular formula C9H9N2O. It is a derivative of the imidazo[1,2-a]pyridine ring system and contains a methyl group at the 5-position. (5-METHYLIMIDAZO[1,2-A]PYRIDIN-3-YL)METHANOL has a hydroxyl (OH) functional group attached to the imidazopyridine ring. It is commonly used in research and pharmaceutical applications due to its potential biological activity.
Used in Pharmaceutical Industry:
(5-METHYLIMIDAZO[1,2-A]PYRIDIN-3-YL)METHANOL is used as a potential drug candidate for the development of new medications. Its unique structure and biological activity make it a promising candidate for further research and development.
Used in Research Applications:
(5-METHYLIMIDAZO[1,2-A]PYRIDIN-3-YL)METHANOL is used as a research tool to understand biochemical processes. Its potential biological activity and unique structure allow researchers to study its interactions with biological systems and explore its potential applications in various fields.

178488-39-6

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178488-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 178488-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,4,8 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 178488-39:
(8*1)+(7*7)+(6*8)+(5*4)+(4*8)+(3*8)+(2*3)+(1*9)=196
196 % 10 = 6
So 178488-39-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O/c1-7-3-2-4-9-10-5-8(6-12)11(7)9/h2-5,12H,6H2,1H3

178488-39-6 Well-known Company Product Price

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  • Aldrich

  • (CBR00499)  (5-Methylimidazo[1,2-a]pyridin-3-yl)methanol  AldrichCPR

  • 178488-39-6

  • CBR00499-1G

  • 1,611.09CNY

  • Detail

  • Aldrich

  • (CBR00499)  (5-Methylimidazo[1,2-a]pyridin-3-yl)methanol  AldrichCPR

  • 178488-39-6

  • CBR00499-1G

  • 1,611.09CNY

  • Detail

  • Aldrich

  • (CBR00499)  (5-Methylimidazo[1,2-a]pyridin-3-yl)methanol  AldrichCPR

  • 178488-39-6

  • CBR00499-1G

  • 1,611.09CNY

  • Detail

  • Aldrich

  • (CBR00499)  (5-Methylimidazo[1,2-a]pyridin-3-yl)methanol  AldrichCPR

  • 178488-39-6

  • CBR00499-1G

  • 1,611.09CNY

  • Detail

178488-39-6SDS

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-MethyliMidazo[1,2-a]pyridin-3-yl)Methanol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

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

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More Details:178488-39-6 SDS

178488-39-6Relevant academic research and scientific papers

Benzimidazolone as potent chymase inhibitor: Modulation of reactive metabolite formation in the hydrophobic (P1) region

Lo, Ho Yin,Nemoto, Peter A.,Kim, Jin Mi,Hao, Ming-Hong,Qian, Kevin C.,Farrow, Neil A.,Albaugh, Daniel R.,Fowler, Danielle M.,Schneiderman, Richard D.,Michael August,Martin, Leslie,Hill-Drzewi, Melissa,Pullen, Steven S.,Takahashi, Hidenori,De Lombaert, Stephane

, p. 4533 - 4539 (2011/09/12)

A new class of chymase inhibitor featuring a benzimidazolone core with an acid side chain and a P1 hydrophobic moiety is described. Incubation of the lead compound with GSH resulted in the formation of a GSH conjugate on the benzothiophene P1 moiety. Replacement of the benzothiophene with different heterocyclic systems such as indoles and benzoisothiazole is feasible. Among the P1 replacements, benzoisothiazole prevents the formation of GSH conjugate and an in silico analysis of oxidative potentials agreed with the experimental outcome.

Synthesis of acyclo-C-nucleosides in the imidazo[1,2-a]pyridine and pyrimidine series as antiviral agents

Gueiffier, Alain,Lhassani, Mohammed,Elhakmaoui, Ahmed,Snoeck, Robert,Andrei, Graciela,Chavignon, Olivier,Teulade, Jean-Claude,Kerbal, Abdelali,Essassi, El Mokhtar,Debouzy, Jean-Claude,Witvrouw, Myriam,Blache, Yves,Balzarini, Jan,De Clercq, Erik,Chapat, Jean-Pierre

, p. 2856 - 2859 (2007/10/03)

The synthesis and the antiviral activities of C-3 acyclic nucleoside analogues of imidazo[1,2-a]pyridine and pyrimidine are reported. From these compounds, 20, 21, 22, 23, 28, and 34 showed a specific activity against cytomegalovirus and/or varicella-zoster virus.

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