91472-94-5

Basic information

• Product Name: 3,3-bis(4-fluorophenyl)propan-1-aMine
• Synonyms: 3,3-bis(4-fluorophenyl)propan-1-aMine
• CAS NO: 91472-94-5
• Molecular Formula: C₁₅H₁₅F₂N
• Molecular Weight: 247.2831064
• Mol File: 91472-94-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3,3-bis(4-fluorophenyl)propan-1-aMine(CAS DataBase Reference)
• NIST Chemistry Reference: 3,3-bis(4-fluorophenyl)propan-1-aMine(91472-94-5)
• EPA Substance Registry System: 3,3-bis(4-fluorophenyl)propan-1-aMine(91472-94-5)

Safety Data

• Hazardous Substances Data: 91472-94-5(Hazardous Substances Data)

Upstream product

• 50775-37-6 3,3-bis(4-fluorophenyl)propionitrile 
• 50775-33-2 3,3-bis(4-fluorophenyl)-3-hydroxypropanenitrile 
• 345-92-6 4,4'-Difluorobenzophenone 
• 50775-35-4 3,3-bis(4-fluorophenyl)-2-propenonitrile 
• 227290-22-4 3,3-bis(4-fluorophenyl)propanamide 
• 1361194-37-7 3,3-bis(4-fluorophenyl)acrylamide 
• 642941-68-2 3-(4-(fluoro)phenyl)acrylamide 

Downstream Products

• 669-19-2 isonicotinic acid-[3,3-bis-(4-fluoro-phenyl)-propylamide] 
• 114667-48-0 N-[3,3-Bis-(4-fluoro-phenyl)-propyl]-N'-[3-(1H-imidazol-4-yl)-propyl]-guanidine 
• 914386-33-7 isoquinoline-3-carboxylic acid [3,3-bis-(4-fluoro-phenyl)-propyl]-amide 
• 914386-71-3 N-[4,4-bis-(4-fluorophenyl)propyl]-6-hydroxy-nicotinamide 
• 914385-94-7 N-[3,3-bis-(4-fluorophenyl)propyl]-4-methanesulfonylbenzamide 
• 1361005-95-9 N-[3,3-bis-(4-fluoro-phenyl)-propyl]-2-(3-fluoro-4-methansulfonylamino-phenyl)-propionamide 

Relevant articles and documents

DUAL INHIBITORS OF SOLUBLE EPOXIDE HYDROLASE AND 5-LIPOXYGENASE

The invention pertains to a novel structure (I) that provides an activity as a dual inhibitor of the enzymes soluble epoxide hydrolase (sEH) and 5-lipoxygenase (5-LOX). The invention pertains to multiple derivatives of the new class of dual inhibitors, their application in medicine, pharmaceutical compositions comprising them as well as to methods for synthesizing the new compounds.

Silver-Catalyzed Long-Distance Aryl Migration from Carbon Center to Nitrogen Center

Selective cleavage of an inert C-C bond followed by C-O/N bond formation through a long-distance aryl migration from a carbon to a nitrogen center via Ag catalysis is reported. The migration products were easily converted into γ-hydroxy amines and tetrahy

N-SUBSTITUTED PYRIDINONE OR PYRIMIDINONE COMPOUNDS USEFUL AS SOLUBLE EPOXIDE HYDROLASE INHIBITORS

Disclosed are compounds of the formula (I) with the definitions of A1 D, Q, W, X, Y and Z as indicated in the description, which are active against soluble epoxide hydrolase (sEH), compositions thereof and methods of using and making same. (I)