720-98-9

Basic information

• Product Name: Phenol, 4-amino-, benzoate (ester)
• CAS NO: 720-98-9
• Molecular Formula: C13H11NO2
• Molecular Weight: 213.236
• Mol File: 720-98-9.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Phenol, 4-amino-, benzoate (ester)(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4-amino-, benzoate (ester)(720-98-9)
• EPA Substance Registry System: Phenol, 4-amino-, benzoate (ester)(720-98-9)

Safety Data

• Hazardous Substances Data: 720-98-9(Hazardous Substances Data)

Upstream product

• 959-22-8 p-nitrophenylbenzoate 
• 80824-77-7 4'-(benzyloxy)benzanilide 
• 15457-50-8 p-benzoylaminophenol 
• 123-30-8 4-amino-phenol 
• 65-85-0 benzoic acid 
• 64-17-5 ethanol 
• 1145-76-2 benzyl 4-nitrophenyl ether 
• 7647-01-0 hydrogenchloride 
• 100-52-7 benzaldehyde 
• 98-88-4 benzoyl chloride 
• 1579-72-2 2,2,2-trifluoroethyl benzoate 
• 1222062-53-4 2-[(4-benzoyloxyphenylamino)methylene]malonic acid diethyl ester 
• 848417-68-5 3,6-dibenzoyloxy-1,2-pyridazine 

Downstream Products

• 69949-84-4 1-benzoyloxy-4-(6-methanesulfinyl-[1,3,4]thiadiazolo[2,3-c][1,2,4]thiadiazol-3-ylideneamino)-benzene 
• 1287767-69-4 4-(bis(3-(triethoxysilyl)propyl)amino)phenyl benzoate 
• 1287767-68-3 4-(3-(triethoxysilyl)propylamino)phenyl benzoate 
• 1287767-70-7 4-(3-(3-(triethoxysilyl)propyl)ureido)phenyl benzoate 
• 1446527-25-8 1-(4-benzoyloxyphenyl)-5-(4-hydroxyphenyl)-3-phenyl-6-oxoverdazyl 
• 1446527-26-9 1-(4-benzoyloxyphenyl)-5-(4-(cyclohexylcarbonyloxy)phenyl)-3-phenyl-6-oxoverdazyl 
• 1446527-24-7 1-(4-benzyloxyphenyl)-5-(4-(4-nitrobenzoyloxy)phenyl)-3-phenyl-6-oxoverdazyl 
• 1446527-23-6 1-(4-benzyloxyphenyl)-5-(4-hydroxyphenyl)-3-phenyl-6-oxoverdazyl 
• 1446527-14-5 1,5-bis(4-benzoyloxyphenyl)-3-phenyl-6-oxoverdazyl 
• 1446527-15-6 1-(4-benzoyloxyphenyl)-5-(4-benzyloxyphenyl)-3-phenyl-6-oxoverdazyl 
• 1446527-33-8 benzaldehyde 4-benzoyloxyphenylhydrazone 
• 1446527-37-2 2,6-bis(4-benzoyloxyphenyl)-4-phenyltetrahydro-1,2,4,5-tetrazin-3(2H)-one 
• 1446527-35-0 benzaldehyde α-chloroformyl 4-benzoyloxyphenylhydrazone 
• 1435955-08-0 (S)-4-[4-(5-aminothiazolo[5,4-d]pyrimidin-7-yl)-3-methylpiperazine-1-carboxamido]-phenyl benzoate 

Relevant articles and documents

Visible-Light Photoredox-Catalyzed and Copper-Promoted Trifluoromethoxylation of Arenediazonium Tetrafluoroborates

We report the development of photoredox-catalyzed and copper-promoted trifluoromethoxylation of arenediazonium tetrafluoroborates, with trifluoromethyl arylsulfonate (TFMS) as the trifluoromethoxylation reagent. This new method takes advantage of visible-light photoredox catalysis to generate the aryl radical under mild conditions, combined with copper-promoted selective trifluoromethoxylation. The reaction is scalable, tolerates a wide range of functional groups, and proceeds regioselectively under mild reaction conditions. Furthermore, mechanistic studies suggested that a Cs[Cu(OCF3)2] intermediate might be generated during the reaction.

HIGHLY CHEMOSELECTIVE REACTIONS IN PRESENCE OF AROMATIC AMINO GROUPS

: The invention discloses a novel process for highly chemoselective reactions of substituted anilines without any detectable reaction at aromatic amino group. The invention also relates to a novel process for preparation of neostigmine methylsulphate via chemoselective reaction of 3-amionphenol and aryl dimethylcarbamates.

Metal-Free Reduction of Aromatic Nitro Compounds to Aromatic Amines with B2pin2 in Isopropanol

A metal-free reduction of aromatic nitro compounds to the corresponding amines has been achieved by a combination of B2pin2 and KOtBu in isopropanol. A series of nitro compounds containing various reducible functional groups were chemoselectively reduced in good to excellent yields.