392-70-1

Basic information

• Product Name: 4-FLUORO-2,6-DIMETHYLANILINE
• Synonyms: 4-FLUORO-2,6-DIMETHYLANILINE;4-Fluoro-2,6-dimethylphenylamine;2-Amino-5-fluoro-m-xylene, 4-Fluoro-2,6-xylidine
• CAS NO: 392-70-1
• Molecular Formula: C₈H₁₀FN
• Molecular Weight: 139.17
• Mol File: 392-70-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 224.5°Cat760mmHg
• Flash Point: 104.6°C
• Appearance: /
• Density: 1.083g/cm³
• Vapor Pressure: 0.0909mmHg at 25°C
• Refractive Index: 1.5345
• Storage Temp.: 2-8°C
• PKA: 4.36±0.10(Predicted)
• CAS DataBase Reference: 4-FLUORO-2,6-DIMETHYLANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-FLUORO-2,6-DIMETHYLANILINE(392-70-1)
• EPA Substance Registry System: 4-FLUORO-2,6-DIMETHYLANILINE(392-70-1)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21/22-36/37/38-22
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 392-70-1(Hazardous Substances Data)

Usage

Uses

4-Fluoro-2,6-dimethylaniline is used as an intermediate.

InChI:InChI=1/C8H10FN/c1-5-3-7(9)4-6(2)8(5)10/h3-4H,10H2,1-2H3

Upstream product

• 315-12-8 2,6-dimethyl-4-fluoro-1-nitro-benzene 
• 461-97-2 3,5-dimethylfluorobenzene 
• 3095-38-3 3,5-dimethyl-4-nitrobenzoic acid 
• 34761-82-5 3,5-dimethyl-4-nitroaniline 
• 19023-45-1 3,5-dimethyl-4-nitro-benzoic acid amide 

Downstream Products

• 443-35-6 chloro-acetic acid-(4-fluoro-2,6-dimethyl-anilide) 
• 14659-61-1 2,6-dimethyl-4-fluorobenzonitrile 
• 2338-56-9 dimethyl-2,6 fluoro-4 phenol 
• 14994-16-2 1-chloro-4-fluoro-2,6-dimethylbenzene 
• 14659-58-6 2‐bromo‐5‐fluoro‐1,3‐dimethylbenzene 
• 14659-59-7 1-iodo-2,6-dimethyl-4-fluorobenzene 
• 16643-18-8 N-(4-fluoro-2,6-dimethylphenyl)acetamide 
• 14994-35-5 5-Fluor-2-dimethylamino-1,3-dimethyl-benzol 
• 584-39-4 2-(diethylamino)-N-(4-fluoro-2,6-dimethylphenyl)acetamide 
• 14659-60-0 methyl 4‐fluoro‐2,6‐dimethylbenzoate 
• 16643-19-9 4-Fluoro-2,6-dimethylbenzamide 
• 16633-50-4 4-fluoro-2,6-dimethyl benzoic acid 
• 1051398-52-7 N,N'-bis(2,6-dimethyl-4-fluorophenyl)ethylenediimine 
• 1099657-26-7 C₁₃H₁₀Cl₂FN₃O 

Relevant articles and documents

Method and using tracer charged ion channel

The invention provides compounds, compositions, methods, and kits for the treatment of pain, itch, and neurogenic inflammation.

π-face donor properties of N-heterocyclic carbenes in grubbs II complexes

The electron-donating properties of eighteen N-heterocyclic carbenes (N,N′-bis(2,6-dimethylphenyl)imidazol)-2-ylidene and the respective dihydro ligands) with 4,4′-R substituted aryl rings (4,4′-R = NEt2, OMe, Me, H, SMe, F, Cl, Br, I) in the r