3,5-Difluoroaniline
3,5-Difluoroaniline
  • CAS No.:372-39-4
Other grades of this product :
3,5-Difluoroaniline Basic information
Synthesis
Product Name:3,5-Difluoroaniline
Synonyms:3,5-Difluoroaniline 98%;3,5-DIFLUOROBENZENEAMINE;3,5-DIFLUOROBENZENAMINE;3,5-DIFLUOROANILINE;3,5-Difluoroaniline(AntibacterialAntiphlogistic,WeedKiller)(C6H5F2N);3,5-Difluoroaniline,98%;Benzenamine, 3,5-difluoro;3,5-Difluoronitroaniline
CAS:372-39-4
MF:C6H5F2N
MW:129.11
EINECS:206-752-8
Product Categories:Fluorobenzene;Anilines, Aromatic Amines and Nitro Compounds;Miscellaneous;Amines;C2 to C6;Nitrogen Compounds;Fluorobenzene Series;bc0001
Mol File:372-39-4.mol
3,5-Difluoroaniline Chemical Properties
Melting point 37-41 °C (lit.)
Boiling point 80°C 20mm
density 1,295 g/cm3
refractive index 1,512-1,514
Fp 167 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
Water Solubility Insoluble in water
form Low Melting Solid
pka2.57±0.10(Predicted)
color White to yellow
BRN 2802286
CAS DataBase Reference372-39-4(CAS DataBase Reference)
EPA Substance Registry System3,5-Difluoroaniline (372-39-4)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21/22-36/37/38
Safety Statements 28-36/37/39-26-36
RIDADR UN 1325 4.1/PG 2
WGK Germany 3
8-10-23
Hazard Note Irritant
TSCA Yes
HazardClass 6.1
PackingGroup III
HS Code 29214200
MSDS Information
ProviderLanguage
3,5-Difluorobenzenamine English
SigmaAldrich English
ACROS English
ALFA English
3,5-Difluoroaniline Usage And Synthesis
SynthesisWork on halogenated benzenes has also demonstrated the versatility of this technique and a variety of fluoro-chloro and -bromo benzenes may be de-brominated and de-chlorinated. Two patents describe removal of chlorine from 2,6-dichloro-3,5- difluoronitrobenzene giving 3,5-difluoroaniline.
Chemical Propertieswhite to yellowish low melting solid
Uses3,5-Difluoroaniline has been used in the preparation of 3,5-difluorodimethylaniline.
General DescriptionIn vitro nephrotoxic effects of 3,5-difluoroaniline has been investigated in renal cortical slices obtained from the kidneys of untreated, male Fischer 344 rats.

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