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369055

Sigma-Aldrich

2-Bromo-4-fluoroaniline

97%

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About This Item

Linear Formula:
BrC6H3(F)NH2
CAS Number:
1003-98-1
Molecular Weight:
190.01
MDL number:
MFCD00042462
UNSPSC Code:
12352100
PubChem Substance ID:
24862951

Assay

97%

form

solid

refractive index

n20/D 1.583 (lit.)

bp

221 °C (lit.)

density

1.67 g/mL at 25 °C (lit.)

functional group

bromo
fluoro

SMILES string

Nc1ccc(F)cc1Br

InChI

1S/C6H5BrFN/c7-5-3-4(8)1-2-6(5)9/h1-3H,9H2

InChI key

YLMFXCIATJJKQL-UHFFFAOYSA-N

General description

2-Bromo-4-fluoroaniline is an aryl fluorinated building block.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

219.2 °F - closed cup

Flash Point(C)

104 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCCB1801
BCBM7672V
BCBJ2184V
BCBB9296V
BCBB9296

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Fatma K Abdel-Wadood et al.
Archiv der Pharmazie, 347(2), 142-152 (2014-01-01)
2-Bromo-4-fluoroaniline (1) was condensed with ethyl 2-cyano-3-ethoxyacrylate (2) in ethanol to afford 3, which upon refluxing in paraffin oil at 250°C gave 8-bromo-3-cyano-6-fluoroquinoline-4(1H)-one (4). Then, compound 4 was taken as a versatile building block that allows the synthesis of thieno[3,2-c]quinoline
Synthesis of fluorescent tetracyclic lactams by a ?one pot? three steps palladium-catalyzed borylation, Suzuki coupling (BSC) and lactamization: DNA and polynucleotides binding studies.
Queiroz M-JRP, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 190(1), 45-52 (2007)
An efficient synthesis of enantiomerically pure aromatic-fused N-containing heterocycles from common chiral aziridines.
Chan Kim J, et al.
Tetrahedron, 66(40), 8108-8114 (2010)

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