85336-82-9

Basic information

• Product Name: Benzeneethanamine, 4-chloro-b-(4-chlorophenyl)-
• CAS NO: 85336-82-9
• Molecular Formula: C14H13Cl2N
• Molecular Weight: 266.17
• Mol File: 85336-82-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzeneethanamine, 4-chloro-b-(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneethanamine, 4-chloro-b-(4-chlorophenyl)-(85336-82-9)
• EPA Substance Registry System: Benzeneethanamine, 4-chloro-b-(4-chlorophenyl)-(85336-82-9)

Safety Data

• Hazardous Substances Data: 85336-82-9(Hazardous Substances Data)

Upstream product

• 52234-91-0 2,2-bis-(4-chloro-phenyl)acetamide 
• 85078-25-7 1,1-bis-(4-chloro-phenyl)-2-nitro-ethane 
• 20968-04-1 2,2’-bis(4-(chloro)phenyl)acetonitrile 
• 83-05-6 bis(4'-chlorophenyl)acetic acid 
• 2642-81-1 1,1-bis(p-chlorophenyl)ethene 

Downstream Products

• 102006-68-8 isonicotinic acid-[2,2-bis-(4-chloro-phenyl)-ethylamide] 
• 101876-76-0 [2,2-bis-(4-chloro-phenyl)-ethyl]-carbamic acid ethyl ester 
• 87519-59-3 (6R,10bS)-9-Chloro-6-(4-chloro-phenyl)-1,5,6,10b-tetrahydro-2H-pyrrolo[2,1-a]isoquinolin-3-one 
• 87519-58-2 (6S,10bS)-9-Chloro-6-(4-chloro-phenyl)-1,5,6,10b-tetrahydro-2H-pyrrolo[2,1-a]isoquinolin-3-one 
• 857530-81-5 2-(4-chloro-phenyl)-2-[4-(1H-pyrazol-4-yl)-phenyl]-ethylamine 
• 87519-88-8 (6R,10bR)-9-Chloro-6-(4-chloro-phenyl)-1,2,3,5,6,10b-hexahydro-pyrrolo[2,1-a]isoquinoline 
• 87519-90-2 9-chloro-6α-(4-chlorophenyl)-1,2,3,5,6,10bβ-hexahydropyrrolo<2,1-a>isoquinoline 
• 90552-79-7 2,2'-{[2,2-Bis(4-chlorophenyl)ethyl]imino}bis{ethanol} 
• 98383-60-9 N₆-(2,2-Di(4-chlorophenyl)ethyl)adenosine 
• 383888-73-1 (2R,3R,4S,5S)-4-(benzoyloxy)-2-(6-{[2,2-bis(4-chlorophenyl)ethyl]amino}-2-iodo-9H-purin-9-yl)-5-[(ethylamino)carbonyl]tetrahydro-3-furanyl benzoate 

Relevant articles and documents

Direct Access to Primary Amines from Alkenes by Selective Metal-Free Hydroamination

Direct and selective synthesis of primary amines from easily available precursors is attractive yet challenging. Herein, we report the rapid synthesis of primary amines from alkenes via metal-free regioselective hydroamination at room temperature. Ammonium carbonate was used as ammonia surrogate for the first time, allowing for efficient conversion of terminal and internal alkenes into linear, α-branched, and α-tertiary primary amines under mild conditions. This method provides a straightforward and powerful approach to a wide spectrum of advanced, highly functionalized primary amines which are of particular interest in pharmaceutical chemistry and other areas.

NOVEL 2-AMINO BENZIMIDAZOLE DERIVATIVES AND THEIR USE AS MODULATORS OF SMALL-CONDUCTANCE CALCIUM-ACTIVATED POTASSIUM CHANNELS

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Antibacterial properties of a series of diarylalkylammonium chlorides.

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