97422-28-1

Basic information

• Product Name: 4-(4-methoxyphenyl)-5-pyridin-3-yl-1,3-thiazol-2-amine
• CAS NO: 97422-28-1
• Molecular Formula: C₁₅H₁₃N₃OS
• Molecular Weight: 283.3482
• Mol File: 97422-28-1.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 472°C at 760 mmHg
• Flash Point: 239.3°C
• Density: 1.275g/cm³
• Vapor Pressure: 4.42E-09mmHg at 25°C
• Refractive Index: 1.648
• CAS DataBase Reference: 4-(4-methoxyphenyl)-5-pyridin-3-yl-1,3-thiazol-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-methoxyphenyl)-5-pyridin-3-yl-1,3-thiazol-2-amine(97422-28-1)
• EPA Substance Registry System: 4-(4-methoxyphenyl)-5-pyridin-3-yl-1,3-thiazol-2-amine(97422-28-1)

Safety Data

• Hazardous Substances Data: 97422-28-1(Hazardous Substances Data)

Upstream product

• 17356-08-0 thiourea 
• 303162-29-0 (4-methoxyphenyl)(2-methylaziridin-1-yl)methanone 
• 108-99-6 3-Methylpyridine 
• 52700-25-1 1-(4-methoxyphenyl)-2-(pyridin-3-yl)-ethanone 
• 100-07-2 4-methoxy-benzoyl chloride 

Relevant articles and documents

Synthesis and biological activities of 4-phenyl-5-pyridyl-1,3-thiazole derivatives as selective adenosine A3 antagonists

To investigate the potency of an adenosine A3 receptor (A 3AR) antagonist as an anti-asthmatic drug, a novel series of 4-phenyl-5-pyridyl-1,3-thiazole derivatives was synthesized and evaluated in human adenosine A1, A

MEDICINAL COMPOSITIONS

The present invention relates to an agent for the prophylaxis or treatment of pain, an agent for suppressing activation of osteoclast, and an inhibitor of osteoclast formation, which contains a p38 MAP kinase inhibitor and/or a TNF-α production inhibitor.

Adenosine A3 receptor antagonists

A pharmaceutical composition for antagonizing adenosine at adenosine A3receptors which comprises a 1,3-azole compound substituted on the 4- or 5-position, or both, by a pyridyl which may be substituted is provided and can be used as a prophylactic and therapeutic agent for asthma, allergosis, inflammation, and so on.