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3,4-Difluoroaniline

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CAS:3863-11-4
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  • 2024-08-14
  • CAS:3863-11-4
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3,4-Difluoroaniline Basic information
Product Name:3,4-Difluoroaniline
Synonyms:3,4-Difluoroaniline, 99+% 2.5ML;Linezolid Aniline Impurity;Linezolid Impurity 95;3,4-Difluoroaniline 98%, 4-Difluoroaniline 98%;3, 4-2 fluoro aniline;TIMTEC-BB SBB007915;3,4-DIFLUOROANILINE;3,4-DIFLUOROBENZENAMINE
CAS:3863-11-4
MF:C6H5F2N
MW:129.11
EINECS:223-381-7
Product Categories:Nitrogen Compounds;Amines;C2 to C6;Anilines, Amides & Amines;Fluorine Compounds;Anilines, Aromatic Amines and Nitro Compounds;Fluorobenzene Series;Fluorine series;bc0001
Mol File:3863-11-4.mol
3,4-Difluoroaniline Structure
3,4-Difluoroaniline Chemical Properties
Melting point 22°C
Boiling point 77 °C/7 mmHg (lit.)
density 1.302 g/mL at 25 °C (lit.)
refractive index n20/D 1.513(lit.)
Fp 185 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka3+-.0.10(Predicted)
form powder to lump to clear liquid
color White or Colorless to Yellow
Specific Gravity1.302
Water Solubility SLIGHTLY SOLUBLE
BRN 971235
InChIInChI=1S/C6H5F2N/c7-5-2-1-4(9)3-6(5)8/h1-3H,9H2
InChIKeyAXNUZKSSQHTNPZ-UHFFFAOYSA-N
SMILESC1(N)=CC=C(F)C(F)=C1
CAS DataBase Reference3863-11-4(CAS DataBase Reference)
NIST Chemistry Reference3,4-Difluoroaniline(3863-11-4)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38-20/21/22
Safety Statements 26-36-36/37/39
RIDADR UN 2941 6.1/PG 3
WGK Germany 3
RTECS CX9871900
8-10-23
Hazard Note Irritant
HazardClass 6.1
PackingGroup III
HS Code 29214200
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
3,4-Difluoroaniline Usage And Synthesis
Chemical Propertiesclear yellow to straw liquid after melting
Uses3,4-Difluoroaniline was used in the synthesis of (3,4-disfluoro)phenylquione.
General Description3,4-Difluoroaniline (3,4-DFA) was degraded, under aerobic conditions, by Pseudomonas fluorescens.
Synthesis
3,4-Difluoronitrobenzene

369-34-6

3,4-Difluoroaniline

3863-11-4

The general procedure for the synthesis of 3,4-difluoroaniline from 3,4-difluoronitrobenzene was as follows: 200.0 g of 3,4-difluoronitrobenzene, 600.0 mL of toluene and 12.0 g of Pd/C catalyst were added to an autoclave at 25 °C to 35 °C. Hydrogen was passed into the reaction system, keeping the hydrogen pressure between 2.0 and 6.0 kg/cm2, and the reaction was carried out at 25 °C to 35 °C for 3 to 4 hours. The progress of the reaction was monitored by thin layer chromatography (TLC) to ensure complete reaction. Upon completion of the reaction, the reaction mixture was sequentially depressurized and unloaded, filtered through a Hyflow bed, and the filter cake was washed with 200.0 mL of toluene. The filtrate was collected and vacuum distilled at less than 50 °C to remove the solvent. Finally, 152.0 g of crude 3,4-difluoroaniline was obtained in 93.8% yield and 95.85% purity by high performance liquid chromatography (HPLC).

References[1] Patent: WO2015/68171, 2015, A1. Location in patent: Page/Page column 9; 16
[2] Tetrahedron Letters, 2010, vol. 51, # 5, p. 786 - 789
[3] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 2, p. 613 - 617
[4] ChemPlusChem, 2018, vol. 83, # 5, p. 375 - 382
[5] Synthesis, 2001, # 1, p. 81 - 84
Tag:3,4-Difluoroaniline(3863-11-4) Related Product Information
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