171881-36-0

Basic information

• Product Name: 5-BroMo-2-(diMethylaMino)benzaldehyde
• Synonyms: 5-BroMo-2-(diMethylaMino)benzaldehyde
• CAS NO: 171881-36-0
• Molecular Formula: C₉H₁₀BrNO
• Molecular Weight: 228.0858
• Mol File: 171881-36-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 5-BroMo-2-(diMethylaMino)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BroMo-2-(diMethylaMino)benzaldehyde(171881-36-0)
• EPA Substance Registry System: 5-BroMo-2-(diMethylaMino)benzaldehyde(171881-36-0)

Safety Data

• Hazardous Substances Data: 171881-36-0(Hazardous Substances Data)

Usage

General Description

5-Bromo-2-(dimethylamino)benzaldehyde is a chemical compound that plays a role in various synthesis reactions in organic chemistry. With a molecular formula of C9H10BrNO, this substance features functional groups of aldehyde and amine, thus taking part in reactions typical for these classes of organic compounds. The bromine atom included in its structure enhances its reactivity making it more susceptible to nucleophilic substitutions. Its derivatives could be applied in various sectors of science and industry, underscoring the significance of this compound for the chemical and pharmaceutical industries.

Upstream product

• 124-40-3 dimethyl amine 
• 93777-26-5 5-bromo-2-fluorobenzaldehyde 
• 73557-58-1 2,4-dibromo-N-methylaniline 
• 64230-27-9 2,4-dibromo-N,N-dimethylaniline 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 171881-24-6 2-(5-bromo-2-dimethylaminophenyl)-2-trimethylsilyloxyacetonitrile 
• 171881-30-4 4-dimethylamino-3-(1,3-dioxolan-2-yl)benzaldehyde 
• 171881-28-0 2-(5-bromo-2-dimethylaminophenyl)-1,3-dioxolane 

Relevant articles and documents

Double Capture of Difluorocarbene by 2-Aminostyrenes Enables the Construction of 3-(2,2-Difluoroethyl)-2-fluoroindoles

We report herein an efficient strategy to construct 3-(2,2-difluoroethyl)-2-fluoroindoles from activated o-aminostyrenes with ethyl bromodi-fluoroacetate as a difluorocarbene source. Through double capture of a difluorocarbene, two different types of fluo

NOVEL CURCUMIN DERIVATIVE

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