111477-17-9

Basic information

• Product Name: IMidazo[1,2-a]pyridine-8-Methanol
• Synonyms: IMidazo[1,2-a]pyridine-8-Methanol;Imidazo[1,2-a]pyridin-8-ylmethanol
• CAS NO: 111477-17-9
• Molecular Formula: C8H8N2O
• Molecular Weight: 148.16192
• Mol File: 111477-17-9.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Density: 1.26±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 13.12±0.10(Predicted)
• CAS DataBase Reference: IMidazo[1,2-a]pyridine-8-Methanol(CAS DataBase Reference)
• NIST Chemistry Reference: IMidazo[1,2-a]pyridine-8-Methanol(111477-17-9)
• EPA Substance Registry System: IMidazo[1,2-a]pyridine-8-Methanol(111477-17-9)

Safety Data

• Hazardous Substances Data: 111477-17-9(Hazardous Substances Data)

Usage

General Description

Imidazo[1,2-a]pyridine-8-methanol, also known as IPA-8-methanol, is a chemical compound with the molecular formula C10H9N2O. It is a derivative of imidazo[1,2-a]pyridine, which is a heterocyclic compound containing both imidazole and pyridine rings. IPA-8-methanol has been studied for its potential pharmacological properties, including its role in modulating serotonin receptors in the brain. It has also been investigated for its potential as a therapeutic agent for conditions such as depression, anxiety, and substance abuse disorders. Additionally, IPA-8-methanol has been studied for its potential use in the development of new drugs targeting the central nervous system. Overall, research on this chemical compound suggests that it may have important implications in the field of pharmaceutical development and neuroscience.

Upstream product

• 107-20-0 2-chloroethanal 
• 23612-57-9 (2-amino-3-pyridinyl)methanol 
• 133427-07-3 methyl 8-imidazo<1,2-a>pyridinecarboxylate 
• 14667-47-1 methyl 2-aminonicotinate 
• 13362-26-0 2-aminopyridine-3-carboxylic acid ethyl ester 
• 158020-74-7 imidazo[1,2-a]pyridine-8-carboxylic acid ethyl ester 

Downstream Products

• 1446321-39-6 2-(imidazo[1,2-a]pyridin-8-ylmethoxy)-5-methoxybenzaldehyde 
• 167883-99-0 8-(chloromethyl)-imidazol[1,2-a]pyridine 
• 372147-63-2 (Z)-ethyl α-[(triphenylphosphoranylideneamino)-β-(imidazo[1,2-a]pyridin-8-yl)]propenoate 
• 136117-74-3 8-imidazo<1,2-a>pyridinecarboxaldehyde 

Relevant articles and documents

SUBSTITUTED BENZALDEHYDE COMPOUNDS AND METHODS FOR THEIR USE IN INCREASING TISSUE OXYGENATION

Provided are substituted benzaldehydes and derivatives thereof that act as allosteric modulators of hemoglobin, methods and intermediates for their preparation, pharmaceutical compositions comprising the modulators, and methods for their use in treating disorders mediate by hemoglobin and disorders that would benefit from increased tissue oxygenation.

BENZISOXAZOLE COMPOUND

Disclosed is a compound represented by the general formula (I) or a salt thereof: wherein any one of R1, R2 and R3 represents a group represented by the formula: -(CH2)m-NR11R12 (wherein m is 1 or 2; and R11 and R12 independently represent a hydrogen atom or a C1-6 alkyl group or may, together with a nitrogen atom to which R11 and R12 are bound, form a 4- or 5-membered cyclic group); the remaining two or R1, R2 and R3 independently represent a group represented by the formula: -(O)n-R21 (wherein n is 0 or 1; and R21 represents a hydrogen atom, a C1-6 alkyl group, a C2-6 alkenyl group, a C2-6 alkynyl group, or the like); and R4 represents a C1-6 alkyl group which may have a substituent or the like.

2-[(Imidazo[1,2-a]pyridinylmethyl)sulfinyl]-1H-benzimidazoles

This invention relates to 2-[(imidazo[1,2-a]pyridinylmethyl)-sulfinyl]-1H-benzimidazoles that are useful in the treatment and prevention of ulcers.