50671-09-5

Basic information

• Product Name: 2-hexadecyloxy-aniline
• CAS NO: 50671-09-5
• Molecular Weight: 333.558
• Mol File: 50671-09-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-hexadecyloxy-aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-hexadecyloxy-aniline(50671-09-5)
• EPA Substance Registry System: 2-hexadecyloxy-aniline(50671-09-5)

Safety Data

• Hazardous Substances Data: 50671-09-5(Hazardous Substances Data)

Upstream product

• 88-75-5 2-hydroxynitrobenzene 
• 112-82-3 hexadecanyl bromide 
• 50671-08-4 hexadecyl-(2-nitro-phenyl)-ether 

Downstream Products

• 1256341-43-1 C₂₉H₄₂N₂O₄ 
• 50670-97-8 5-(2-Cetoxybenzolsulfamoyl)-α-chlor-α-(2-fluorbenzoyl)-2-methoxyacetanilid 
• 50671-30-2 α-(2-Fluorbenzoyl)-5-(2-cetoxybenzolsulfamoyl)-2-methoxyacetanilid 
• 50670-88-7 α-Chlor-α-(2-chlorbenzoyl)-2-cetoxyacetanilid 
• 50670-89-8 α-Chlor-α-(2-fluorbenzoyl)-2-cetoxyacetanilid 
• 50671-29-9 3-Amino-4-methoxybenzolsulfo-(2-cetoxy)-anilin 
• 2489-55-6 3-{3-[2-(2-Hexadecyloxy-phenylcarbamoyl)-acetyl]-phenylsulfamoyl}-benzenesulfonyl fluoride 
• 2489-54-5 3-{3-[2-(2-Hexadecyloxy-phenylcarbamoyl)-acetyl]-phenylcarbamoyl}-benzenesulfonyl fluoride 
• 2489-51-2 3-(3-Amino-phenyl)-N-(2-hexadecyloxy-phenyl)-3-oxo-propionamide 
• 50671-10-8 2-Cetoxy-α-(2-chlorbenzoyl)-acetanilid 
• 50671-11-9 2-Cetoxy-α-(2-fluorbenzoyl)-acetanilid 
• 50671-28-8 4-Methoxy-3-nitrobenzolsulfo-(2-cetoxy)-anilid 
• 2489-38-5 4-[2-(2-Hexadecyloxy-phenylcarbamoyl)-acetyl]-benzenesulfonyl fluoride 
• 2489-37-4 3-[2-(2-Hexadecyloxy-phenylcarbamoyl)-acetyl]-benzenesulfonyl fluoride 

Relevant articles and documents

Synthesis and biological evaluation of novel N-(alkoxyphenyl)-aminocarbonylbenzoic acid derivatives as PTP1B inhibitors

Based on the fact that petroselinic acid showed good inhibitory activity (IC50=6.99μmol/L) against protein tyrosine phophatase 1B(PTP1B) in vitro, a series of novel N-(alkoxyphenyl)-aminocarbonylbenzoic acid derivatives were designed and synthesized. The results indicated that most of the derivatives showed more potent activities against PTP1B. Especially, compound 13 had obvious activity with an IC50 of 106nmol/L in vitro.