4-Fluoro-5-nitrobenzene-1,2-diamine

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4-Fluoro-5-nitrobenzene-1,2-diamine Basic information
Product Name:4-Fluoro-5-nitrobenzene-1,2-diamine
Synonyms:4-Fluoro-5-nitrobenzene-1,2-diamine , Tech.;4,5-Diamine-2-fluoronitrobenzene;4-fluoro-5-nitro-2-aMino-aniline;4,5-Diamino-2-fluoronitrobenzene, 4-Fluoro-5-nitrophenylene-1,2-diamine;1,2-Benzenediamine, 4-fluoro-5-nitro-;4-Fluoro-5-nitro-1,2-benzenediamine;4-Fluoro-5-nitrobenzene-1,2-diamine
CAS:113269-06-0
MF:C6H6FN3O2
MW:171.13
EINECS:
Product Categories:
Mol File:113269-06-0.mol
4-Fluoro-5-nitrobenzene-1,2-diamine Structure
4-Fluoro-5-nitrobenzene-1,2-diamine Chemical Properties
Boiling point 438.4±40.0 °C(Predicted)
density 1.555±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka1.95±0.10(Predicted)
AppearanceBrown to reddish brown Solid
InChIInChI=1S/C6H6FN3O2/c7-3-1-4(8)5(9)2-6(3)10(11)12/h1-2H,8-9H2
InChIKeyQZNALIMEKAACKP-UHFFFAOYSA-N
SMILESC1(N)=CC([N+]([O-])=O)=C(F)C=C1N
Safety Information
HS Code 2921511990
MSDS Information
4-Fluoro-5-nitrobenzene-1,2-diamine Usage And Synthesis
Synthesis
1,2-DITOSYLAMINO-4-FLUORO-5-NITROBENZENE

113269-03-7

4-FLUORO-5-NITROBENZENE-1,2-DIAMINE

113269-06-0

General procedure for the synthesis of 4-fluoro-5-nitrobenzene-1,2-diamine from N,N'-(4-fluoro-5-nitro-1,2-phenylene)bis(4-methylbenzenesulfonamide): 158 mg (0.33 mmol) N-[4-fluoro-5-nitro-2-(4-toluenesulfonylamino)-phenyl]-4-methylbenzenesulfonamide was suspended in a mixture of 35 μL deionized water and 360 μL of concentrated sulfuric acid in a mixed solution, and the suspension was heated at 80 °C for 1 hour. Upon completion of the reaction, the reaction mixture was poured into 10 mL of deionized water and a yellow solid was precipitated. The aqueous suspension was heated to boiling to completely dissolve the solid and subsequently cooled to room temperature. The pH of the solution was adjusted to about 9 with concentrated ammonia, at which point an orange solid precipitated. The solid product was separated by filtration, washed with deionized water and dried in air. A final product of 49 mg was obtained in 88% yield.

References[1] Heterocycles, 1987, vol. 26, # 9, p. 2433 - 2442
[2] Patent: US2006/4197, 2006, A1. Location in patent: Page/Page column 12/16; 8; 16
4-Fluoro-5-nitrobenzene-1,2-diamine Preparation Products And Raw materials
Raw materials1,2-Ditosylamino-4-fluoro-5-nitrobenzene-->Ammonia-->Sulfuric acid
Tag:4-Fluoro-5-nitrobenzene-1,2-diamine(113269-06-0) Related Product Information
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