92028-21-2

Basic information

• Product Name: 3-Phenyl-4-methoxyaniline hydrochloride
• Synonyms: 3-PHENYL-4-METHOXYANILINE HYDROCHLORIDE;3-PHENYL-4-ANISIDINE HYDROCHLORIDE;3-PHENYL-P-ANISIDINE HYDROCHLORIDE;4-PHENYL-M-ANISIDINE HCL;3-Phenyl-4-methoxyaniline;6-Methoxy-[1,1'-biphenyl]-3-aMine hydrochloride;4-methoxy-3-phenylaniline,hydrochloride
• CAS NO: 92028-21-2
• Molecular Formula: C₁₃H₁₃NO*ClH
• Molecular Weight: 235.71
• EINECS: 1312995-182-4
• Mol File: 92028-21-2.mol

Chemical Properties

• Melting Point: 237-240°C
• Boiling Point: 340.1ºC at 760 mmHg
• Flash Point: 166.2ºC
• Appearance: off-white solid
• Density: g/cm³
• Vapor Pressure: 8.78E-05mmHg at 25°C
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 3-Phenyl-4-methoxyaniline hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Phenyl-4-methoxyaniline hydrochloride(92028-21-2)
• EPA Substance Registry System: 3-Phenyl-4-methoxyaniline hydrochloride(92028-21-2)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 92028-21-2(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Synthesis:
3-Phenyl-4-methoxyaniline hydrochloride is utilized as a key intermediate in the synthesis of various pharmaceutical drugs. Its unique structure allows for the creation of new molecules with potential therapeutic applications.
Used in Organic Chemistry:
3-Phenyl-4-methoxyaniline hydrochloride serves as a reagent in organic chemistry reactions, facilitating the introduction of phenyl and methoxy functional groups into a range of molecules, thereby expanding the scope of chemical synthesis and the development of new chemical entities.
Used in Medical Research:
3-Phenyl-4-methoxyaniline hydrochloride is employed in medical research for its ability to interact with specific molecular targets, which can be crucial in understanding and modulating biological processes related to various diseases and conditions.
Used in Biochemical Research:
The hydrochloride salt form of the compound enhances its stability and solubility in aqueous solutions, making it an ideal candidate for use in biochemical research where interactions with biological systems are studied.

InChI:InChI=1/C13H13NO.ClH/c1-15-13-8-7-11(14)9-12(13)10-5-3-2-4-6-10;/h2-9H,14H2,1H3;1H

Downstream Products

• 530084-71-0 C₃₃H₃₆N₂O₃ 
• 530084-77-6 N-{2-[4-(3-phenyl-4-methoxyphenyl)aminophenyl]ethyl}-(R)-2-tert-butyldimethylsilyl-2-(8-benzyloxy-2(1H)-quinolinon-5-yl)ethylamine 
• 372093-19-1 N-(4-Methoxy-3-phenyl)phenyl-(2-chloro-5-nitrophenyl)carboxamide 
• 96003-82-6 DL-N-Acetyl-3-<3,5-dinitro-4-(4-methoxy-3-phenyl-phenoxy)-phenyl>-2-amino-propionsaeure-ethylester 
• 95945-26-9 DL-N-Acetyl-3-<3,5-diiod-4-(4-methoxy-3-phenyl-phenoxy)-phenyl>-2-amino-propionsaeure-ethylester 
• 25119-48-6 DL-3,5-Diiod-3'-phenyl-thyronin