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1027074-50-5

2-(4-bromophenyl)-3-iodoimidazo[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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  • 1027074-50-5 Structure

  • Basic information

    1. Product Name: 2-(4-bromophenyl)-3-iodoimidazo[1,2-a]pyridine
    2. Synonyms: 2-(4-bromophenyl)-3-iodoimidazo[1,2-a]pyridine
    3. CAS NO:1027074-50-5
    4. Molecular Formula:
    5. Molecular Weight: 399.028
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1027074-50-5.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-bromophenyl)-3-iodoimidazo[1,2-a]pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-bromophenyl)-3-iodoimidazo[1,2-a]pyridine(1027074-50-5)
    11. EPA Substance Registry System: 2-(4-bromophenyl)-3-iodoimidazo[1,2-a]pyridine(1027074-50-5)

  • 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: 1027074-50-5(Hazardous Substances Data)

1027074-50-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1027074-50-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,0,7 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1027074-50:
(9*1)+(8*0)+(7*2)+(6*7)+(5*0)+(4*7)+(3*4)+(2*5)+(1*0)=115
115 % 10 = 5
So 1027074-50-5 is a valid CAS Registry Number.

1027074-50-5Relevant articles and documents

Difluorinative-hydroxylation and C-3 functionalization (halogenation/SCN/NO) of imidazopyridine using Selectfluor as fluorine source or oxidant respectively

Balasubramanian, Sridhar,Kalari, Saradhi,Rode, Haridas B.

, (2021)

An efficient route for the difluorinative-hydroxylation through dearomative difunctionalization of imidazopyridine using Selectfluor as fluorine source has been developed in an aqueous medium. The reaction proceeds through ionic followed by radical pathwa

K2S2O8-Mediated halogenation of 2-arylimidazo[1,2-a]pyridines using sodium halides as the halogen sources

Katrun, Praewpan,Kuhakarn, Chutima

, p. 989 - 993 (2019)

A convenient halogenation of 2-arylimidazo[1,2-a]pyridines using sodium chloride/bromide/iodide as the halogen sources in the presence of K2S2O8 as an easy-to-handle oxidizing agent was developed. The present work offers a

Electrochemical oxidative iodination of imidazo[1,2-a]pyridines using NaI as iodine source

Park, Jin Wha,Kim, Yong Hwan,Kim, Dae Young

, p. 710 - 718 (2020)

An electrochemical oxidative iodination of imidazo[1,2-a]pyridines is achieved in this study. This reaction utilizes NaI as an iodine source and a supporting electrolyte under metal-free and exogenous chemical oxidant-free reaction conditions. The present

Condensed-cyclic compound and organic light emitting diode comprising the same

-

, (2016/11/17)

Disclosed are a carbazole-based compound and an organic light-emitting device comprising the same. The carbazole-based compound is represented by chemical formula 1. The organic light-emitting device comprising the carbazole-based compound can have a low

Heterogeneous biomimetic aerobic synthesis of 3-iodoimidazo[1,2-a]pyridines via CuOx/OMS-2-catalyzed tandem cyclization/iodination and their late-stage functionalization

Meng, Xu,Yu, Chaoying,Chen, Gexin,Zhao, Peiqing

, p. 372 - 379 (2015/02/02)

In the presence of copper supported on manganese oxide-based octahedral molecular sieves OMS-2 (CuOx/OMS-2), the heterogeneously catalytic, aerobic synthesis of 3-iodoimidazo[1,2-a]pyridines from acetophenones, 2-aminopyridines and I2/sub

Phenanthro[2,3-b]pyrroles and Phenanthro[3,2-b]pyrroles for organic light-emitting devices

-

, (2011/04/18)

Embodiments of the present invention are directed to a heterocyclic compound and an organic light-emitting device including the heterocyclic compound. The organic light-emitting devices using the heterocyclic compounds have high-efficiency, low driving vo

IMIDAZOPYRIDINE-BASED COMPOUND AND ORGANIC LIGHT EMITTING DIODE INCLUDING ORGANIC LAYER COMPRISING THE IMIDAZOPYRIDINE-BASED COMPOUND

-

Page/Page column 12-13, (2008/12/05)

Imidazopyridine-based compounds and organic light emitting diodes (OLEDs) including organic layers including the imidazopyridine-based compounds are provided. The organic light emitting diodes including organic layers having the imidazopyridine-based compounds have low driving voltages, high efficiencies, high luminance, long life-times and low power consumption.

Imidazopyridine-based compounds and organic light emitting diode including organic layer comprising the imidazopyridine-based compounds

-

Page/Page column 16-17, (2008/12/05)

Imidazopyridine-based compounds of Formula I and organic light emitting diodes (OLEDs) comprising organic layers including the imidazopyridine-based compounds are provided. The organic light emitting diodes including organic layers having the imidazopyridine-based compounds have low driving voltages, high efficiencies, high luminance, long life-times and low power consumption.

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