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Imidazo[1,2-a]pyridine-2-carboxaldehyde, 8-bromois a heterocyclic chemical compound with the molecular formula C9H6BrN3O. It features a fused imidazopyridine ring structure, a carboxaldehyde functional group, and a bromine atom attached to the 8th position. Imidazo[1,2-a]pyridine-2-carboxaldehyde, 8-bromoholds promise in medicinal chemistry as a precursor for the synthesis of innovative pharmaceuticals with potential therapeutic properties, leveraging its distinctive structural and reactive attributes for drug discovery and development.

1194375-12-6

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1194375-12-6 Usage

Uses

Used in Medicinal Chemistry:
Imidazo[1,2-a]pyridine-2-carboxaldehyde, 8-bromoserves as a key building block for the synthesis of novel pharmaceutical compounds. Its unique structure and reactivity make it a valuable component in the creation of new drugs with potential biological activities.
Used in Drug Discovery:
Imidazo[1,2-a]pyridine-2-carboxaldehyde, 8-bromois utilized in drug discovery processes to explore its potential as a precursor for developing new therapeutic agents. Its chemical properties and structural features are exploited to create molecules that may exhibit desired pharmacological effects.
Used in Pharmaceutical Development:
In the pharmaceutical industry, Imidazo[1,2-a]pyridine-2-carboxaldehyde, 8-bromois employed as a starting material for the development of new drugs. Its role is crucial in the synthesis of compounds that could address unmet medical needs or improve upon existing treatments.
Used in Chemical Research:
Imidazo[1,2-a]pyridine-2-carboxaldehyde, 8-bromois also used in academic and industrial chemical research settings. Researchers investigate its properties and reactivity to understand its behavior in various chemical reactions and to identify new applications in chemical synthesis and compound design.

Check Digit Verification of cas no

The CAS Registry Mumber 1194375-12-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,4,3,7 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1194375-12:
(9*1)+(8*1)+(7*9)+(6*4)+(5*3)+(4*7)+(3*5)+(2*1)+(1*2)=166
166 % 10 = 6
So 1194375-12-6 is a valid CAS Registry Number.

1194375-12-6SDS

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 8-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names QC-8778

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:1194375-12-6 SDS

1194375-12-6Downstream Products

1194375-12-6Relevant academic research and scientific papers

SUBSTITUTED BICYCLIC IMIDAZOLE DERIVATIVES AS GAMMA SECRETASE MODULATORS

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Page/Page column 60, (2010/08/05)

The present invention is concerned with novel substituted bicyclic imidazole derivatives of Formula (I) wherein R0, R1, R3, R4, X, A1, A2, A3, A4, Y1, Y2 and Y3 have the meaning defined in the claims. The compounds according to the present invention are useful as gamma secretase modulators. The invention further relates to processes for preparing such novel compounds, pharmaceutical compositions comprising said novel compound as an active ingredient as well as the use of said compounds as a medicament.

Imidazopyridine-5,6,7,8-tetrahydro-8-quinolinamine derivatives with potent activity against HIV-1

Gudmundsson, Kristjan S.,Boggs, Sharon D.,Catalano, John G.,Svolto, Angilique,Spaltenstein, Andrew,Thomson, Michael,Wheelan, Pat,Jenkinson, Stephen

scheme or table, p. 6399 - 6403 (2010/05/02)

Synthesis of several novel imidazopyridine-5,6,7,8-tetrahydro-8-quinolinamine derivatives with potent activity against HIV are described. Synthetic approaches allowing for variation of the substitution pattern are outlined and resulting changes in antivir

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