26271-75-0

Basic information

• Product Name: 3,5-dichloro-1,4-aminophenol
• Synonyms: 3,5-dichloro-1,4-aminophenol;4-Amino-3,5-dichlorophenol
• CAS NO: 26271-75-0
• Molecular Formula: C₆H₅Cl₂NO
• Molecular Weight: 178.02
• Mol File: 26271-75-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 294°Cat760mmHg
• Flash Point: 131.6°C
• Appearance: /
• Density: 1.56g/cm³
• Vapor Pressure: 0.00095mmHg at 25°C
• Refractive Index: 1.661
• CAS DataBase Reference: 3,5-dichloro-1,4-aminophenol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-dichloro-1,4-aminophenol(26271-75-0)
• EPA Substance Registry System: 3,5-dichloro-1,4-aminophenol(26271-75-0)

Safety Data

• Hazardous Substances Data: 26271-75-0(Hazardous Substances Data)

Usage

Uses

4-Amino-3,5-dichlorophenol is a useful research chemical compound.

InChI:InChI=1/C6H5Cl2NO/c7-4-1-3(10)2-5(8)6(4)9/h1-2,10H,9H2

Upstream product

• 637-62-7 p-benzoquinone oxime 
• 51225-20-8 1,3-dichloro-5-ethoxy-2-aminobenzene 
• 50590-08-4 3,5-dichloro-4-nitrophenol 
• 857623-82-6 5-acetoxy-2-acetylamino-1,3-dichloro-benzene 
• 7647-01-0 hydrogenchloride 
• 60-29-7 diethyl ether 
• 10034-85-2 hydrogen iodide 
• 2623-33-8 4-acetoxyacetanilide 
• 60144-85-6 4'-acetoxy-2'-chloroacetanilide 
• 591-35-5 3,5-dichlorophenol 
• 15307-86-5 [2-(2,6-dichloroanilino)phenyl]acetic acid 

Downstream Products

• 609-19-8 3,4,5-trichlorophenol 
• 3336-19-4 2,6-dichloro-4-hydroxy-benzonitrile 
• 697-91-6 2,6-dichloro-1,4-benzoquinone 
• 37055-88-2 N-2,6-Dichlorphenylschwefelharnstoff 
• 303049-40-3 4-Tosylamino-3,5-dichlorophenol 
• 100-32-3 di(p-nitrophenyl) disulfide 
• 5147-73-9 N-[(4-nitrophenyl)thio]-2,6-dichloro-1,4-benzoquinone imine 
• 103-19-5 di(p-tolyl) disulfide 
• 5335-87-5 4,4'-dimethoxyphenyl disulfide 
• 1142-19-4 4,4'-dichlorodiphenyl disulfide 
• 303049-41-4 N-Tosyl-3,5-dichloro-1,4-benzoquinonemonoimine 
• 500878-30-8 3,4,5-trichloro-2,6-bis-hydroxymethyl-phenol 
• 213747-80-9 N-(3,5-dichloro-4-hydroxyphenyl)-4-(3,5-dimethylphenylsulphanyl)-2-pyrimidineamine 

Relevant articles and documents

TiO2-modified MALDI target for in vitro modeling of the oxidative biotransformation of diclofenac

The UV-induced photocatalytic oxidation in the presence of TiO2 nanoparticles (UV/TiO2-PCO) is a more adequate approach than electrochemical oxidation to simulate the oxidative metabolism of diclofenac based on the comparative analysis of oxidation products using high-resolution tandem mass spectrometry. A simple and fast high-throughput technique is proposed for modeling the oxidative metabolism, which involves UV/TiO2-PCO performed directly on a MALDI target and subsequent analysis by matrix-assisted laser desorption/ionization mass spectrometry. The ranges and yields of diclofenac oxidation products obtained by the conventional bulk UV/TiO2-PCO and the proposed on-target version are in excellent agreement.