57775-06-1

Basic information

• Product Name: 2-(2-Bromophenyl)-2-methylpropanenitrile
• Synonyms: 2-(2-Bromophenyl)-2-methylpropanenitrile;2-(2-Bromo-phenyl)-2-methyl-propionitrile
• CAS NO: 57775-06-1
• Molecular Formula: C₁₀H₁₀BrN
• Molecular Weight: 224.0971
• Mol File: 57775-06-1.mol

Chemical Properties

• Boiling Point: 95-105 °C(Press: 0.03 Torr)
• Appearance: /
• Density: 1.352±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-(2-Bromophenyl)-2-methylpropanenitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-Bromophenyl)-2-methylpropanenitrile(57775-06-1)
• EPA Substance Registry System: 2-(2-Bromophenyl)-2-methylpropanenitrile(57775-06-1)

Safety Data

• Hazardous Substances Data: 57775-06-1(Hazardous Substances Data)

Usage

Nitrile derivative

Functional group This compound contains a nitrile functional group (C≡N), which is a strong electron-withdrawing group that can participate in various chemical reactions.

Bromophenyl and methylpropane groups

Substituents The nitrile functional group is attached to a bromophenyl group (Br-C6H4) and a methylpropane group (CH3-CH2-CH2-), which provide the compound with its unique chemical properties.

Organic synthesis building block

Synthesis applications 2-(2-Bromophenyl)-2-methylpropanenitrile is commonly used in organic synthesis to construct various pharmaceuticals, agrochemicals, and other fine chemicals.

Reagent for bromine and nitrile group introduction

Chemical reactions This compound can be used as a reagent in chemical reactions to introduce bromine and nitrile groups into organic molecules, which can be important for the synthesis of target compounds with desired properties.

Potential applications in new materials

Material development 2-(2-Bromophenyl)-2-methylpropanenitrile may have potential applications in the development of new materials due to its unique chemical structure and properties.

Intermediate for complex organic compound synthesis

Synthesis applications The compound can also serve as an intermediate for the synthesis of more complex organic compounds, which can be further modified or functionalized to achieve desired properties and applications.

Upstream product

• 19472-74-3 2-(2-bromophenyl)acetonitrile 
• 74-88-4 methyl iodide 
• 1072-85-1 o-fluorobromobenzene 
• 78-82-0 Isobutyronitrile 

Downstream Products

• 71095-49-3 2-bromo-β,β-dimethylbenzeneethanamine 
• 212626-89-6 2-(2-bromophenyl)-2-methylpropionaldehyde 
• 173026-22-7 2-bromo-α,α-dimethylbenzeneacetamide 
• 173026-23-8 2-bromo-α,α-dimethylbenzenemethanamine 
• 212627-00-4 4-(2-bromophenyl)-4-methylpentanoic acid ethyl ester 
• 19155-24-9 3,3-dimethyloxindole 
• 1422148-83-1 2-(2-bromophenyl)-N,2-dimethylpropanamide 
• 1422148-84-2 N-benzyl-2-(2-bromophenyl)-2-methylpropanamide 
• 1422148-86-4 2-(2-bromophenyl)-2-methyl-N-tosylpropanamide 
• 1422148-87-5 N-acetyl-2-(2-bromophenyl)-2-methylpropanamide 
• 114081-14-0 1-benzyl-3,3-dimethyl-1,3-dihydro-indol-2-one 
• 36797-34-9 3,3-dimethyl-1-tosylindolin-2-one 
• 1430563-78-2 methyl 2-(2-bromophenyl)-2-methylpropylcarbamate 
• 1203684-57-4 5-bromo-4,4-dimethyl-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

Diastereoselective Construction of Eight-Membered Carbocycles through Palladium-Catalyzed C(sp3)-H Functionalization

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Synthesis of Amides and Esters by Palladium(0)-Catalyzed Carbonylative C(sp3)?H Activation

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