13726-14-2

Basic information

• Product Name: 4-Chloro-3-methoxyaniline
• Synonyms: 2-CHLORO-5-AMINOANISOLE;4-CHLORO-3-METHOXYANILINE;4-CHLORO-M-ANISIDINE;5-Amino-2-chloroanisole;3-Methoxy-4-chloroaniline;4-Chloro-m-anisidine 5-Amino-2-chloroanisole 2-Chloro-5-aminoanisole;5-Amino-2-chloroanisole, 4-Chloro-m-anisidine;5-AMino-2-chloroanisole[4-Chloro-3-Methoxyaniline]
• CAS NO: 13726-14-2
• Molecular Formula: C₇H₈ClNO
• Molecular Weight: 157.6
• Product Categories: Amines;blocks;Anilines, Aromatic Amines and Nitro Compounds;Anilines, Amides & Amines;Anisoles, Alkyloxy Compounds & Phenylacetates;Chlorine Compounds
• Mol File: 13726-14-2.mol
• Article Data: 22

Chemical Properties

• Melting Point: 77-79
• Boiling Point: 274.058 °C at 760 mmHg
• Flash Point: 119.546 °C
• Appearance: /
• Density: 1.234 g/cm³
• Vapor Pressure: 0.006mmHg at 25°C
• Refractive Index: 1.573
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• Solubility: DMSO (Slightly), Methanol (Slightly)
• PKA: 3.54±0.10(Predicted)
• CAS DataBase Reference: 4-Chloro-3-methoxyaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Chloro-3-methoxyaniline(13726-14-2)
• EPA Substance Registry System: 4-Chloro-3-methoxyaniline(13726-14-2)

Safety Data

• Hazard Codes: Xi
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39-36/37
• RIDADR: UN2233
• HazardClass: 6.1
• PackingGroup: III
• Hazardous Substances Data: 13726-14-2(Hazardous Substances Data)

Usage

Uses

4-Chloro-3-methoxyaniline is a useful reagent for the preparation of Raf kinase inhibitors.

InChI:InChI=1/C7H8ClNO/c1-10-7-4-5(9)2-3-6(7)8/h2-4H,9H2,1H3

Upstream product

• 1984-58-3 2,5-dichloroanisole 
• 7664-41-7 ammonia 
• 553-82-2 1,3-dichloro-4-methoxybenzene 
• 16817-43-9 5-Bromo-2-chloroanisole 
• 1236162-19-8 C₇H₇ClINO 
• 1009-36-5 2-chloro-5-nitroanisole 
• 7439-89-6 iron 
• 49735-71-9 2-methoxy-4-nitrobenzene diazonium 1,5-naphthalene disulfonate 
• 97-52-9 2-methoxy-4-nitrophenylamine 

Downstream Products

• 102236-59-9 4-chloro-3-methoxy-N,N-dimethyl-aniline 
• 120222-86-8 4-chloro-3-methoxy-phenyl isothiocyanate 
• 18113-07-0 4-Chloro-3-methoxyphenol 
• 43096-00-0 N-[4-(4-Chloro-3-methoxy-phenylamino)-9,10-dioxo-9,10-dihydro-anthracen-1-yl]-benzamide 
• 86726-32-1 2-Chloro-3-(4-chloro-3-methoxy-phenyl)-propionic acid methyl ester 
• 13726-16-4 4-chloro-3-methoxybenzaldehyde 
• 16817-43-9 5-Bromo-2-chloroanisole 
• 103209-95-6 4-(5-chloro-6-methoxy-benzotriazol-2-yl)-stilbene-2-sulfonic acid dibutylamide 
• 334710-28-0 (4-chloro-3-methoxy-phenyl)-carbamic acid tert-butyl ester 
• 28170-67-4 N-(4-chloro-3-methoxyphenyl)-N,N'-dimethylurea 
• 161949-50-4 1-chloro-4-iodo-2-methoxybenzene 
• 92668-54-7 3-(4-Chloro-3-methoxy-phenyl)-5,5-dimethyl-imidazolidine-2,4-dione 
• 26378-41-6 2-(4-Chloro-3-methoxy-phenoxy)-ethylamine 
• 26378-47-2 5-(2-Amino-ethoxy)-2-chloro-phenol 

Relevant articles and documents

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High catalytic activity of a new Ag phosphorus ylide complex supported on montmorillonite: synthesis, characterization, and application for room temperature nitro reduction

In this work, the phosphorus ylide, [PPh3CHC(O)CH2Cl], was reacted with AgNO3 to give the [Ag{C(H)PPh3C(O)CH2Cl}2]+NO3? as the product. Then, it was supported on the modified montmorillonite nanoclay to prepare a new catalyst for the reduction reaction. The structure and morphology of the nanoclay catalyst were characterized by FT-IR, X-ray powder diffraction, scanning electron microscopy, energy-dispersive X-ray analysis and transmission electron microscopy techniques; also, the content of silver was obtained by inductively coupled plasma analyzer. This composition was exploited to study its catalytic activity in the reduction in aromatic nitro compounds; it displayed the high catalytic activity. Factors such as catalyst amount, solvent, temperature and reaction time were all systematically investigated to elucidate their effects on the yield of catalytic reduction in nitroarenes. This catalytic system exhibited high activity toward aromatic nitro compounds under mild conditions. The catalyst was reused five times without any significant loss in its catalytic activity.

FE NANOPARTICLES WITH PPM CONTENTS OF PD, CU AND/OR NI, REACTIONS IN WATER CATALYZED BY THEM

The present application discloses a nanoparticle composition prepared from a mixture comprising: a) a transition metal salt; b) an iron salt; and c) a reducing agent; and methods for the use of such compositions, including the reduction of an organic compound comprising a nitro group to form an organic compound comprising an amine group, the Cu-catalyzed cyclization of an azide and an alkyne (click chemistry) and cross coupling reactions, notably Suzuki-Miyaura reactions. The transition metal salts are in particular Pd, Cu and Ni salts, the content of these metals being typically in the ppm range based on the major constituent Fe in the final products.