Cas 552855-95-5,N-tert-butyl-2-(4-fluorophenyl)-1H-imidazo[1,2-a]pyridine-3-amine

552855-95-5

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Basic information

Product Name: N-tert-butyl-2-(4-fluorophenyl)-1H-imidazo[1,2-a]pyridine-3-amine
Synonyms: N-tert-butyl-2-(4-fluorophenyl)-1H-imidazo[1,2-a]pyridine-3-amine
CAS NO:552855-95-5
Molecular Formula:
Molecular Weight: 283.348
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-tert-butyl-2-(4-fluorophenyl)-1H-imidazo[1,2-a]pyridine-3-amine(CAS DataBase Reference)
NIST Chemistry Reference: N-tert-butyl-2-(4-fluorophenyl)-1H-imidazo[1,2-a]pyridine-3-amine(552855-95-5)
EPA Substance Registry System: N-tert-butyl-2-(4-fluorophenyl)-1H-imidazo[1,2-a]pyridine-3-amine(552855-95-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 552855-95-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 552855-95-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,2,8,5 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 552855-95:
(8*5)+(7*5)+(6*2)+(5*8)+(4*5)+(3*5)+(2*9)+(1*5)=185
185 % 10 = 5
So 552855-95-5 is a valid CAS Registry Number.

552855-95-5Upstream product

552855-95-5Downstream Products

504-29-0 2-aminopyridine

552855-95-5Relevant academic research and scientific papers

Efficient synthesis of 3-Aminoimidazo[1,2-a] pyridines using silica-supported perchloric acid (HClO4-SiO2) as a novel heterogenous catalyst

Habibi, Azizollah,Tarameshloo, Zahra,Rostamizadeh, Shahnaz,Amani, Ali M.

, p. 155 - 159 (2012)

One pot three-component reaction of 2-amino pyridines, aldehydes and isocyanides in the presence of silicasupported perchloric acid (HClO 4-SiO2), produces 3-aminoimidazo[1,2-a] pyridines in excellent yields. The reaction time is sho

Diverse Oxidative C(sp2)-N Bond Cleavages of Aromatic Fused Imidazoles for Synthesis of α-Ketoamides and N-(pyridin-2-yl)arylamides

Xu, Fangzhou,Wang, Yanyan,Xun, Xiwei,Huang, Yun,Jin, Zhichao,Song, Baoan,Wu, Jian

, p. 8411 - 8422 (2019/05/17)

An efficient and chemoselective C(sp2)-N bond cleavage of aromatic imidazo[1,2-a]pyridine molecules is developed. A broad scope of amide compounds such as α-ketoamides and N-(pyridin-2-yl)arylamides are afforded as the final products in up to quantitative yields. Diverse C-N bond cleavages are controlled by the oxidative species used in this transformation, with various amide products afforded in a chemoselective fashion. A preliminary study indicated that some α-ketoamides exhibit anti-Tobacco Mosaic Virus activity for potential use in plant protection.

An efficient, regioselective, versatile synthesis of N-fused 2- and 3-aminoimidazoles via Ugi-type multicomponent reaction mediated by zirconium(IV) chloride in polyethylene glycol-400

Guchhait, Sankar K.,Madaan, Chetna

scheme or table, p. 628 - 632 (2009/07/01)

An Ugi-type multicomponent reaction of heterocyclic amidines with aldehydes and isocyanides catalyzed by zirconium(IV) chloride in PEG-400 was developed. The protocol offers the rapid, environment friendly, regioselective and versatile synthesis of medici

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