61057-85-0

Basic information

• Product Name: alpha-(2-AMinophenyl)benzylaMine
• Synonyms: alpha-(2-AMinophenyl)benzylaMine;2-amino-α-phenyl-benzenemethanamine;2-Amino-alpha-phenylbenzylamine;2-Aminobenzhydrylamine;2-(Amino(phenyl)methyl)aniline
• CAS NO: 61057-85-0
• Molecular Formula: C₁₃H₁₄N₂
• Molecular Weight: 198.26366
• Mol File: 61057-85-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: alpha-(2-AMinophenyl)benzylaMine(CAS DataBase Reference)
• NIST Chemistry Reference: alpha-(2-AMinophenyl)benzylaMine(61057-85-0)
• EPA Substance Registry System: alpha-(2-AMinophenyl)benzylaMine(61057-85-0)

Safety Data

• Hazardous Substances Data: 61057-85-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Alpha-(2-aminophenyl)benzylamine is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new chemical entities with potential therapeutic applications. Its structural features facilitate the creation of diverse drug candidates that can target a range of health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, alpha-(2-aminophenyl)benzylamine serves as a crucial building block in the synthesis of various agrochemicals. Its incorporation into these compounds can enhance their effectiveness in agricultural applications, such as pest control and crop protection.
Used in Organic Chemistry Research:
As a versatile intermediate, alpha-(2-aminophenyl)benzylamine is also used in organic chemistry research for exploring its potential in forming new compounds with unique properties. This research can lead to advancements in material science, chemical engineering, and the discovery of novel applications for alpha-(2-AMinophenyl)benzylaMine.
Used in Neuroprotective and Anti-Inflammatory Applications:
Due to its potential neuroprotective and anti-inflammatory properties, alpha-(2-aminophenyl)benzylamine is studied for use in therapeutic applications aimed at treating neurological disorders and conditions characterized by inflammation. Its presence in drug development pipelines underscores its importance in the search for new treatments in these areas.

Upstream product

• 71-43-2 benzene 
• 1885-29-6 anthranilic acid nitrile 
• 51674-05-6 1-(2-Aminophenyl)-1-phenyl-methanonoxim 

Downstream Products

• 84571-42-6 2-(1H-Indol-3-yl)-4-phenyl-1,2,3,4-tetrahydro-quinazoline 
• 84570-92-3 2-(4-Nitro-phenyl)-4-phenyl-1,2,3,4-tetrahydro-quinazoline 
• 84571-04-0 2,4-Diphenyl-1,2,3,4-tetrahydro-quinazoline 
• 84571-78-8 C₂₅H₃₄N₂ 
• 84602-13-1 C₁₈H₂₀N₂ 
• 84571-13-1 2-(2-Nitro-phenyl)-4-phenyl-1,2,3,4-tetrahydro-quinazoline 
• 84571-72-2 C₂₀H₂₄N₂ 
• 111039-29-3 [3-Oxo-5-phenyl-5H-thiazolo[2,3-b]quinazolin-(2Z)-ylidene]-acetic acid methyl ester 
• 75614-96-9 5-Phenyl-5,11-dihydroisoindolo<2,1-a>chinazolin 
• 84571-32-4 4-Chloro-2-(4-phenyl-1,2,3,4-tetrahydro-quinazolin-2-yl)-phenol 
• 84571-51-7 2,2-Dimethyl-4-phenyl-1,2,3,4-tetrahydro-quinazoline 
• 84570-90-1 Dimethyl-[4-(4-phenyl-1,2,3,4-tetrahydro-quinazolin-2-yl)-phenyl]-amine 
• 84571-07-3 2-(2-Methoxy-phenyl)-4-phenyl-1,2,3,4-tetrahydro-quinazoline 
• 84571-53-9 2-Methyl-2,4-diphenyl-1,2,3,4-tetrahydro-quinazoline 

Relevant articles and documents

Superelectrophilic chemistry of amino-nitriles and related substrates

The superacid-promoted Houben/Hoesch reactions of amino-nitriles and related compounds have been studied. The nitriles form dicationic electrophiles and react with benzene in fair to good yields (12-95%). The intermediate iminium ions may also be reduced to the benzylic amines by NaBH4 or H 2.