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1452807-18-9

2-(4-fluorophenyl)-3-nitroimidazo[1,2-a]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1452807-18-9 Structure

  • Basic information

    1. Product Name: 2-(4-fluorophenyl)-3-nitroimidazo[1,2-a]pyridine
    2. Synonyms: 2-(4-fluorophenyl)-3-nitroimidazo[1,2-a]pyridine
    3. CAS NO:1452807-18-9
    4. Molecular Formula:
    5. Molecular Weight: 257.224
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1452807-18-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(4-fluorophenyl)-3-nitroimidazo[1,2-a]pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-fluorophenyl)-3-nitroimidazo[1,2-a]pyridine(1452807-18-9)
    11. EPA Substance Registry System: 2-(4-fluorophenyl)-3-nitroimidazo[1,2-a]pyridine(1452807-18-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1452807-18-9(Hazardous Substances Data)

1452807-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1452807-18-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,2,8,0 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1452807-18:
(9*1)+(8*4)+(7*5)+(6*2)+(5*8)+(4*0)+(3*7)+(2*1)+(1*8)=159
159 % 10 = 9
So 1452807-18-9 is a valid CAS Registry Number.

1452807-18-9Downstream Products

1452807-18-9Relevant articles and documents

Magnetic carbon nanotube supported Cu (CoFe2O4/CNT-Cu) catalyst: A sustainable catalyst for the synthesis of 3-nitro-2-arylimidazo[1,2-a]pyridines

Zhang, Mo,Lu, Jun,Zhang, Jia-Nan,Zhang, Zhan-Hui

, p. 26 - 32 (2016/02/23)

A magnetic carbon nanotube supported Cu catalyst (CoFe2O4/CNT-Cu) was prepared, characterized and evaluated as a recoverable catalyst for synthesis of 3-nitro-2-arylimidazo[1,2-a]pyridines via one-pot three-component reactions of 2-a

Synthesis of 3-Nitro-2-arylimidazo[1,2- a ]pyridines Using Sodium Dichloro?-iodide

Jagadhane, Prashant B.,Telvekar, Vikas N.

, p. 2636 - 2638 (2015/01/09)

Moderate to good yields of various 3-nitro-2-arylimidazo[1,2-a]pyridines have been easily achieved in the reaction of 2-aminopyridines and nitrostyrenes in the presence of sodium dichloriodide. The procedure is simple and various functional groups are tol

Synthesis of 3-nitro-2-arylimidazo[1,2- a ]pyridines using sodium dichloro-iodide

Jagadhane, Prashant B.,Telvekar, Vikas N.

, (2015/08/06)

Moderate to good yields of various 3-nitro-2-arylimidazo[1,2-a]pyridines have been easily achieved in the reaction of 2-aminopyridines and nitrostyrenes in the presence of sodium dichloriodide. The procedure is simple and various functional groups are tol

Bu4NI-catalyzed synthesis of imidazo[1,2- a ]pyridines via oxidative coupling of aminopyridines with nitroolefins

Xu, Xiangsheng,Hu, Peizhu,Yu, Wubin,Hong, Guo,Tang, Yucai,Fang, Mingwu,Li, Xiaoqing

, p. 718 - 720 (2014/04/03)

A metal-free method for the synthesis of imidazo[1,2-a]pyridines via double C-N oxidative coupling of aminopyridines with nitroolefins using TBAI as the catalyst and TBHP as oxidation agent has been developed. Georg Thieme Verlag Stuttgart. New York.

Exploration of versatile reactions on 2-chloro-3-nitroimidazo[1,2-a] pyridine: Expanding structural diversity of C2- and C3-functionalized imidazo[1,2-a]pyridines

Bazin, Marc-Antoine,Marhadour, Sophie,Tonnerre, Alain,Marchand, Pascal

, p. 5378 - 5382 (2013/09/12)

Alternative strategies for functionalizing 2-chloro-3-nitroimidazo[1,2-a] pyridine have been developed. Suzuki-Miyaura cross-coupling reaction provided easily the corresponding 2-arylated compounds, and herefrom the nitro group was reduced into amine which afforded amides, anilines, and ureas in the 3-position. The amination of the key compound using a metal-catalyzed reaction was reported. This study highlighted the importance of the nitro group to facilitate the chlorine displacement. Other nucleophilic aromatic substitutions open a route to various products derived from imidazo[1,2-a]pyridine.

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