1430074-80-8

Basic information

• Product Name: ethyl 3-(4-(trifluoromethyl)phenyl)imidazo[1,5-α]pyridine-1-carboxylate
• Synonyms: ethyl 3-(4-(trifluoromethyl)phenyl)imidazo[1,5-α]pyridine-1-carboxylate
• CAS NO: 1430074-80-8
• Molecular Weight: 334.298
• Mol File: 1430074-80-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl 3-(4-(trifluoromethyl)phenyl)imidazo[1,5-α]pyridine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3-(4-(trifluoromethyl)phenyl)imidazo[1,5-α]pyridine-1-carboxylate(1430074-80-8)
• EPA Substance Registry System: ethyl 3-(4-(trifluoromethyl)phenyl)imidazo[1,5-α]pyridine-1-carboxylate(1430074-80-8)

Safety Data

• Hazardous Substances Data: 1430074-80-8(Hazardous Substances Data)

Upstream product

• 1451194-94-7 C₁₇H₁₅F₃N₂O₃ 
• 55243-15-7 aminopyridin-2-ylacetic acid ethyl ester 
• 71721-67-0 ethyl 2-hydroxyimino-2-(pyridin-2-yl)acetate 
• 2739-98-2 ethyl 2-(pyridinyl-2)acetate 
• 3300-51-4 p-Trifluoromethylbenzylamine 

Downstream Products

• 1451194-92-5 C₁₅H₉F₃N₂O₂ 
• 1451194-90-3 C₂₄H₂₅F₃N₄O₃ 
• 1380811-30-2 C₁₉H₁₇F₃N₄O 
• 1380810-68-3 C₃₉H₄₅F₃N₆O₆S₂ 
• 1380810-73-0 C₄₀H₄₇F₃N₆O₆S₂ 
• 1380810-76-3 C₄₁H₄₉F₃N₆O₆S₂ 
• 1380810-78-5 C₄₂H₅₁F₃N₆O₆S₂ 
• 1380810-08-1 C₃₅H₃₅F₃N₆O₄ 
• 1380810-09-2 C₃₆H₃₇F₃N₆O₄ 
• 1380810-11-6 C₃₇H₃₉F₃N₆O₄ 
• 1380810-14-9 C₃₈H₄₁F₃N₆O₄ 
• 1380810-71-8 C₃₉H₄₇F₃N₆O₄S₂ 
• 1380810-75-2 C₄₀H₄₉F₃N₆O₄S₂ 
• 1380810-77-4 C₄₁H₅₁F₃N₆O₄S₂ 

Relevant articles and documents

Metal-free synthesis of imidazo[1,5- a] pyridines via elemental sulfur mediated sequential dual oxidative Csp3-H amination

A simple and efficient approach has been developed for the synthesis of imidazo[1,5-a]pyridines using the elemental sulfur mediated sequential dual oxidative Csp3-H amination of 2-pyridyl acetates and amines under metal- and peroxide-free conditions. Broad substrate scope, operational simplicity and gram-scale ability make this chemistry very practical.

Mild metal-free sequential dual oxidative amination of C(sp3)-H bonds: Efficient synthesis of imidazo[1,5-a]pyridines

A metal-free sequential dual oxidative amination of C(sp3)-H bonds under ambient conditions was the first developed, affording imidazo[1,5-a]pyridines in good to excellent yields. The reaction was involved in two oxidative C-N couplings and one oxidative dehydrogenation process with six hydrogen atoms removed.