30489-44-2 Usage
General Description
(2-Methylimidazo[1,2-a]pyridin-3-yl)methanol, also known as MIPM, is a chemical compound with the molecular formula C9H9NO. It is a derivative of imidazo[1,2-a]pyridine, which is a heterocyclic compound with potential pharmacological properties. MIPM has been studied for its potential use in medicinal chemistry, particularly as a building block for the synthesis of biologically active compounds. Its structure includes a methyl group attached to the imidazo[1,2-a]pyridine ring, which may influence its chemical and pharmacological properties. Further research is needed to fully understand the potential applications and effects of (2-Methylimidazo[1,2-a]pyridin-3-yl)methanol.
Check Digit Verification of cas no
The CAS Registry Mumber 30489-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,4,8 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 30489-44:
(7*3)+(6*0)+(5*4)+(4*8)+(3*9)+(2*4)+(1*4)=112
112 % 10 = 2
So 30489-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H10N2O/c1-7-8(6-12)11-5-3-2-4-9(11)10-7/h2-5,12H,6H2,1H3
30489-44-2Relevant articles and documents
METHYL SULFANYL PYRMIDMES USEFUL AS ANTIINFLAMMATORIES, ANALGESICS, AND ANTIEPILEPTICS
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Page/Page column 178-179, (2010/12/18)
The present invention relates to pyrimidine derivatives of Formula (Ia) and (Ib) (including tautomers, isomers, prodrugs, and pharmaceutically acceptable salts thereof). Said compounds are useful in the treatment of pain (such as neuropathic pain), inflammation, and epilepsy (by acting as anticonvulsants). Methods of medical treatment making use of said compounds, as well as additional compounds of Formula (IIa) and (IIb), are also disclosed.
Synthesis and biological activity of 3-substituted imidazo[1,2-a]pyridines as antiulcer agents
Starrett Jr.,Montzka,Crosswell,Cavanagh
, p. 2204 - 2210 (2007/10/02)
New imidazo[1,2-a]pyridines substituted at the 3-position have been synthesized as potential antisecretory and cytoprotective antiulcer agents. The synthetic routes began with cyclization of aminopyridines 5a,b and chloro ketones 6a,b to give imidazo[1,2-