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1-Fluoro-2,4-dinitrobenzene / 10 X 1 G

Purity: 99.0% (GC)
Synonym: DNFB; DNPF; FDNB; Sanger reagent; Dinitrofluorobenzene; 2,4-Dinitro-1-fluorobenzene
Molecular Formula: (O2N)2C6H3F; C6H3FN2O4
Molecular Weight: 186.10
SKU: MND-7272
CAS Number: 70-34-8
MDL number: MFCD00007056
EC Number: 200-734-3
Form: (Solid or Semi-Solid or Chunk(s) or Paste or Liquid)
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 10 X 1 G  
237.30 EUR



Safety Information


Hazard Statements

H302
H315
H319
H335
H373
H317

Precautionary Statements

P280
P301 + P312
P305 + P351 + P338
P302 + P352
P260
P314
P301 + P312 + P330

Pictograms



Properties

Signal WordWarning
Flash Point (C)164 °C
Flash Point (F)327.2 °F
Boiling Point178 °C/25 mmHg (lit.)
Melting Point25-27 °C (lit.)

 Product Description

1-Fluoro-2,4-dinitrobenzene is a chemical compound utilized as a building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. It is valued for its reactivity and ability to introduce fluorine-containing functional groups into organic molecules.

 

Application:

1-Fluoro-2,4-dinitrobenzene is commonly employed as a fluorinating agent in organic synthesis, enabling the introduction of fluorine atoms into various compounds. It is utilized in the pharmaceutical and agrochemical industries for the production of fluorinated intermediates and final products.

 

 

 

Articles:

- Reaction of Myosin with 1-Fluoro-2,4-dinitrobenzene at Low Ionic Strength

Publication Date: Available online 10 February 1969

M Bárány, G Bailin, K Bárány

https://doi.org/10.1016/S0021-9258(18)94404-2

 

- The α-Effect in SNAr Reaction of 1-Fluoro-2,4-dinitrobenzene with Hydrazine: Ground-State Destabilization versus Transition-State Stabilization

Publication Date: 2014.08.20

Cho, Hyo-Jin; Um, Ik-Hwan

https://doi.org/10.5012/bkcs.2014.35.8.2371

 

- Molecular Rearrangement in the Reaction of Cysteine with 1-Fluoro-2,4-Dinitrobenzene

Publication Date: 04 January 1958

H. P. BURCHFIELD

https://doi.org/10.1038/181049b0