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Imidazo[1,2-a]pyridine, 2-bromo-6-methoxyis a heterocyclic aromatic compound with the molecular formula C9H7BrN2O. It belongs to the class of imidazo[1,2-a]pyridine compounds and features a bromo and a methoxy group, which confer unique reactivity and properties to the molecule. This chemical compound serves as a valuable building block in organic chemistry research and drug development due to its structural and functional characteristics. It may also find potential applications in the agricultural and pharmaceutical industries.

1042141-33-2

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1042141-33-2 Usage

Uses

Used in Organic Chemistry Research:
Imidazo[1,2-a]pyridine, 2-bromo-6-methoxyis used as a chemical intermediate for the synthesis of various organic compounds. Its unique reactivity and properties make it a valuable building block in organic chemistry research.
Used in Drug Development:
Imidazo[1,2-a]pyridine, 2-bromo-6-methoxyis used as a key component in the development of new pharmaceuticals. Its structural properties allow for the creation of novel drug candidates with potential therapeutic applications.
Used in Agricultural Industry:
Imidazo[1,2-a]pyridine, 2-bromo-6-methoxymay be used as a chemical component in the development of new agrochemicals, such as pesticides or herbicides, due to its unique structural properties.
Used in Pharmaceutical Industry:
Imidazo[1,2-a]pyridine, 2-bromo-6-methoxyis used as a potential active pharmaceutical ingredient or as a precursor in the synthesis of new drugs. Its unique structural properties may contribute to the development of innovative therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 1042141-33-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,2,1,4 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1042141-33:
(9*1)+(8*0)+(7*4)+(6*2)+(5*1)+(4*4)+(3*1)+(2*3)+(1*3)=82
82 % 10 = 2
So 1042141-33-2 is a valid CAS Registry Number.

1042141-33-2 Well-known Company Product Price

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  • Aldrich

  • (ADE001237)  2-Bromo-6-methoxyimidazo[1,2-a]pyridine  AldrichCPR

  • 1042141-33-2

  • ADE001237-1G

  • 7,411.95CNY

  • Detail

1042141-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-6-methoxyimidazo[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:1042141-33-2 SDS

1042141-33-2Upstream product

1042141-33-2Downstream Products

1042141-33-2Relevant academic research and scientific papers

AROMATIC RING DERIVATIVE AS IMMUNOREGULATION AND PREPARATION METHOD AND APPLICATION OF AROMATIC RING DERIVATIVE

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Paragraph 0155-0156, (2021/10/15)

Relating to a compound represented by formula (I) and a pharmaceutically acceptable salt of the compound, and an application of the compound as an S1P1 agonist.

NOVEL HETEROARYL SUBSTITUTED IMIDAZO [1,2 -A] PYRIDINE DERIVATIVES

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Page/Page column 48-49, (2008/12/07)

The present invention relates to novel heteroaryl substituted imidazopyridine derivatives, precursors thereof, and therapeutic uses of such compounds, having the structural formula (Ia) and to their pharmaceutically acceptable salt, compositions and methods of use. Furthermore, the invention relates to novel heteroaryl substituted imidazopyridine derivatives that are suitable for imaging amyloid deposits in living patients, their compositions, methods of use and processes to make such compounds. More specifically, the present invention relates to a method of imaging amyloid deposits in brain in vivo to allow antemortem diagnosis of Alzheimer's disease as well as measureing clinical efficacy of Alzheimer's disease therapeutic agents.

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