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539112

Sigma-Aldrich

4-Bromo-1-fluoro-2-nitrobenzene

96%

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25 G
PLN 760.00

PLN 760.00

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25 G
PLN 760.00

About This Item

Linear Formula:
BrC6H3(F)NO2
CAS Number:
364-73-8
Molecular Weight:
220.00
MDL number:
MFCD00129165
UNSPSC Code:
12352100
PubChem Substance ID:
24878380
NACRES:
NA.22

PLN 760.00

Please contact Customer Service for Availability
Request a Bulk Order

Quality Level

100

Assay

96%

refractive index

n20/D 1.575 (lit.)

bp

240-241 °C (lit.)

mp

18-19 °C (lit.)

density

1.786 g/mL at 25 °C (lit.)

functional group

bromo
fluoro
nitro

SMILES string

[O-][N+](=O)c1cc(Br)ccc1F

InChI

1S/C6H3BrFNO2/c7-4-1-2-5(8)6(3-4)9(10)11/h1-3H

InChI key

UQEANKGXXSENNF-UHFFFAOYSA-N

Related Categories

General description

4-Bromo-1-fluoro-2-nitrobenzene undergoes Sonogashira reaction with 2-fluoronitrobenzene to afford predominantly the bromo displacement product.[1]

Application

4-Bromo-1-fluoro-2-nitrobenzene may be used in the synthesis of:
  • 6-bromo-1H-benzo[d][1,2,3]triazol-1-ol[2]
  • 2-(4-bromo-2-nitrophenylamino)-5-methylthiophene-3-carbonitrile[3]
  • dibenzoxazepine analog, as potent sodium channel blocker[4]
  • 4-(4-bromo-2-nitrophenyl)piperazine-1-carboxylic acid tert-butylester[5]
Used in the synthesis of anti-inflammatory agents.[6]

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW3721
MKCL6565
MKBW8750V
MKBW3201V
MKBT6168V

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As a first trial for in vivo imaging of β-secretase (BACE1) in Alzheimer's disease brain, we applied a novel non-peptidergic small molecule which has high affinity to the enzyme, naphthalene-1-carboxylic acid (3'-chloro-4'-fluoro-4-piperazin-1-yl-biphenyl-3-yl)amide (NCFB) into positron emission tomography (PET) probe. In
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Advanced synthesis & catalysis, 357(2-3), 451-462 (2015-03-03)
Benzotriazoles are a highly important class of compounds with broad-ranging applications in such diverse areas as medicinal chemistry, as auxiliaries in organic synthesis, in metallurgical applications, in aircraft deicing and brake fluids, and as antifog agents in photography. Although there
Katie M Lutker et al.
Crystal growth & design, 8(1), 136-139 (2008-01-01)
Bis(5-methyl-2-[(2-nitrophenyl)amino]-3-thiophenecarbonitrilyl)acetylene, a derivative of the highly polymorphic compound 5-methyl-2-[(2-nitrophenyl)amino]-3-thiophenecarbonitrile (ROY) that possesses two chromophores electronically coupled through a triple bond, was found to be trimorphic. Structural data for two of these forms indicates that symmetry is maintained in one structure
Patrick L DeRoy et al.
Organic letters, 9(14), 2741-2743 (2007-06-08)
The nucleophilic aromatic substitution reaction between electron-deficient aryl fluorides and terminal alkynes is shown to be efficiently promoted by sodium bis(trimethylsilyl)amide as a base. Moderate to excellent yields of 2-ethynylnitrobenzene products can be obtained under mild conditions.
Erik Rytter Ottosen et al.
Journal of medicinal chemistry, 46(26), 5651-5662 (2003-12-12)
We wish to report the synthesis and structure-activity relationship (SAR) of a series of 4-aminobenzophenones, as a novel compound class with high antiinflammatory activity. Our initial lead, (4-[(2-aminophenyl)amino]phenyl)(phenyl)methanone (3), was systematically optimized and resulted in compounds that potently inhibited the
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