104498-78-4

Basic information

• Product Name: 5-(4-Amino-phenyl)-pentanoic acid methyl ester
• Synonyms: 5-(4-Amino-phenyl)-pentanoic acid methyl ester
• CAS NO: 104498-78-4
• Molecular Weight: 207.272
• Mol File: 104498-78-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 5-(4-Amino-phenyl)-pentanoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-Amino-phenyl)-pentanoic acid methyl ester(104498-78-4)
• EPA Substance Registry System: 5-(4-Amino-phenyl)-pentanoic acid methyl ester(104498-78-4)

Safety Data

• Hazardous Substances Data: 104498-78-4(Hazardous Substances Data)

Upstream product

• 555-16-8 4-nitrobenzaldehdye 
• 61346-08-5 5-(p-Nitrophenyl)-pentansaeuremethylester 

Downstream Products

• 279669-91-9 3-[(E)-7-(4-Amino-phenyl)-3-hydroxy-hept-1-enyl]-cyclohexanone 
• 279669-92-0 3-[(E)-7-(4-Azido-phenyl)-3-hydroxy-hept-1-enyl]-cyclohexanone 
• 279669-93-1 3-[(E)-7-(4-Amino-3-iodo-phenyl)-3-hydroxy-hept-1-enyl]-cyclohexanone 
• 279669-94-2 3-[(E)-7-(4-Azido-3-iodo-phenyl)-3-hydroxy-hept-1-enyl]-cyclohexanone 
• 279669-88-4 diethyl 2-oxo-6-(4-tritylamino)phenylhexylphosphonate 
• 279669-89-5 (E)-1-(1,4-Dioxa-spiro[4.5]dec-7-yl)-7-[4-(trityl-amino)-phenyl]-hept-1-en-3-one 
• 279669-90-8 (E)-1-(1,4-Dioxa-spiro[4.5]dec-7-yl)-7-[4-(trityl-amino)-phenyl]-hept-1-en-3-ol 
• 130031-43-5 Acridin-9-yl-(4-{4-[bis-(2-chloro-ethyl)-amino]-phenyl}-butyl)-amine 
• 1001406-46-7 Bis-(2-chloro-ethyl)-[4-(4-isocyanato-butyl)-phenyl]-amine 
• 130198-83-3 [4-(4-Amino-butyl)-phenyl]-bis-(2-chloro-ethyl)-amine 
• 64508-90-3 5-{4-[bis-(2-chloro-ethyl)-amino]-phenyl}-valeric acid 
• 279669-87-3 5-[4-(trityl-amino)-phenyl]-pentanoic acid methyl ester 
• 130198-77-5 5-{4-[Bis-(2-hydroxy-ethyl)-amino]-phenyl}-pentanoic acid methyl ester 

Relevant articles and documents

Leukotriene B4 photoaffinity probes: design, synthesis and evaluation of new arylazide-1,3-disubstituted cyclohexanes.

The synthesis and the binding affinities of new leukotriene B4 receptor photoaffinity probes, where a 1,3-disubstituted cyclohexane ring replaces the conjugated delta6,7 and delta8,9 double bonds of the natural eicosanoid, are described. One enantiomeric compound, 4b alpha, is specifically cross-linked upon photolysis to the recombinant leukotriene B4 receptor from human origin (h-BLTR) solubilized in a micellar medium. This probe appears as a good candidate for identifying the ligand binding site of this receptor.