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321945-25-9

6-Bromo-2-(4-nitro-phenyl)-imidazo[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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  • 321945-25-9 Structure

  • Basic information

    1. Product Name: 6-Bromo-2-(4-nitro-phenyl)-imidazo[1,2-a]pyridine
    2. Synonyms: Imidazo[1,2-a]pyridine, 6-bromo-2-(4-nitrophenyl)-
    3. CAS NO:321945-25-9
    4. Molecular Formula: C13H8BrN3O2
    5. Molecular Weight: 316.98
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 321945-25-9.mol

  • Chemical Properties

    1. Melting Point: >250 °C(Solv: pyridine (110-86-1))
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.67 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 4.45±0.50(Predicted)
    10. CAS DataBase Reference: 6-Bromo-2-(4-nitro-phenyl)-imidazo[1,2-a]pyridine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 6-Bromo-2-(4-nitro-phenyl)-imidazo[1,2-a]pyridine(321945-25-9)
    12. EPA Substance Registry System: 6-Bromo-2-(4-nitro-phenyl)-imidazo[1,2-a]pyridine(321945-25-9)

  • 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: 321945-25-9(Hazardous Substances Data)

321945-25-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 321945-25-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,9,4 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 321945-25:
(8*3)+(7*2)+(6*1)+(5*9)+(4*4)+(3*5)+(2*2)+(1*5)=129
129 % 10 = 9
So 321945-25-9 is a valid CAS Registry Number.

321945-25-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-2-(4-nitrophenyl)imidazo[1,2-a]pyridine

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:321945-25-9 SDS

321945-25-9Downstream Products

321945-25-9Relevant articles and documents

Imidazo[1,2- a]pyridine derivatives as aldehyde dehydrogenase inhibitors: Novel chemotypes to target glioblastoma stem cells

Quattrini, Luca,Gelardi, Edoardo Luigi Maria,Coviello, Vito,Sartini, Stefania,Ferraris, Davide Maria,Mori, Mattia,Nakano, Ichiro,Garavaglia, Silvia,La Motta, Concettina

, p. 4603 - 4616 (2020/06/08)

Glioblastoma multiforme (GBM) is the deadliest form of brain tumor. It is known for its ability to escape the therapeutic options available to date thanks to the presence of a subset of cells endowed with stem-like properties and ability to resist to cyto

Oxidative Cross-Coupling of sp3- and sp2-Hybridized C-H Bonds: Vanadium-Catalyzed Aminomethylation of Imidazo[1,2-a]pyridines

Kaswan, Pinku,Porter, Ashley,Pericherla, Kasiviswanadharaju,Simone, Marissa,Peters, Sean,Kumar, Anil,Deboef, Brenton

supporting information, p. 5208 - 5211 (2015/11/18)

The vanadium-catalyzed oxidative coupling of substituted 2-arylimidiazo[1,2-a]pyridines to N-methylmorpholine oxide, which acts as both a coupling partner and an oxidant, has been achieved. This reaction was applied to various substituted imidiazo[1,2-a]pyridine and indole substrates, resulting in yields as high as 90%. Mechanistic investigations indicate that the reaction may proceed via a Mannich-type process. This work demonstrates how oxidative aminomethylation can be used as a useful method to introduce tertiary amines into heterocycles, thus providing an alternative method for conventional Mannich-type reactions.

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