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3-Bromo-7-methyl-imidazo[1,2-a]pyridine is a halogenated derivative of the heterocyclic aromatic compound imidazo[1,2-a]pyridine, characterized by the molecular formula C8H7BrN2. This chemical compound is recognized for its unique structure and reactivity, which makes it a valuable building block in the synthesis of pharmaceuticals and agrochemicals. Its potential pharmaceutical applications and known biological activity have positioned it as a subject of interest in drug discovery and development, with ongoing research in medicinal chemistry and organic synthesis aimed at exploring its synthesis and characteristics.

56051-32-2

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56051-32-2 Usage

Uses

Used in Pharmaceutical Industry:
3-Bromo-7-methyl-imidazo[1,2-a]pyridine is used as a key intermediate in the synthesis of various pharmaceutical compounds for its unique structural and reactive properties. It contributes to the development of new drugs by providing a versatile platform for chemical modifications that can enhance the pharmacological properties of the final drug products.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Bromo-7-methyl-imidazo[1,2-a]pyridine is utilized as a building block in the creation of agrochemicals, such as pesticides and herbicides. Its reactivity and structural features allow for the design of effective compounds that can target specific pests or weeds, thereby increasing the efficiency and selectivity of these agrochemicals in agricultural applications.
Used in Drug Discovery and Development:
3-Bromo-7-methyl-imidazo[1,2-a]pyridine is employed as a starting material in drug discovery and development processes due to its demonstrated biological activity. Researchers leverage its chemical properties to design and synthesize new molecules with potential therapeutic effects, contributing to the advancement of novel treatments for various diseases and conditions.
Used in Medicinal Chemistry Research:
3-Bromo-7-methyl-imidazo[1,2-a]pyridine serves as a subject of study in medicinal chemistry, where its synthesis and characteristics are investigated to understand its potential role in the development of pharmaceutical agents. This research helps in identifying new pathways for drug design and optimization, ultimately leading to the creation of more effective and safer medications.

Check Digit Verification of cas no

The CAS Registry Mumber 56051-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,5 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56051-32:
(7*5)+(6*6)+(5*0)+(4*5)+(3*1)+(2*3)+(1*2)=102
102 % 10 = 2
So 56051-32-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7BrN2/c1-6-2-3-11-7(9)5-10-8(11)4-6/h2-5H,1H3

56051-32-2 Well-known Company Product Price

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  • Aldrich

  • (L510920)  3-Bromo-7-methylimidazo[1,2-a]pyridine  AldrichCPR

  • 56051-32-2

  • L510920-1G

  • 2,575.17CNY

  • Detail

56051-32-2SDS

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 3-Bromo-7-methylimidazo[1,2-a]pyridine

1.2 Other means of identification

Product number -
Other names 3-bromo-7-methylimidazo[1,2-a]pyridine

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:56051-32-2 SDS

56051-32-2Relevant academic research and scientific papers

Transition-metal-free regioselective C-H halogenation of imidazo[1,2-: A] pyridines: Sodium chlorite/bromite as the halogen source

Li, Junxuan,Tang, Jiayi,Wu, Yuanheng,He, Qiuxing,Yu, Yue

, p. 5058 - 5062 (2018)

A facile transition-metal-free regioselective halogenation of imidazo[1,2-a]pyridines using sodium chlorite/bromite as the halogen source is presented. The reaction has provided an efficient method for the formation of C-Cl or C-Br bonds to synthesize 3-c

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