2-Bromo-3-fluoroaniline

CAS Number: 111721-75-6

Molecular Formula: C6H5BrFN

2-Bromo-3-fluoroaniline supplierbuy 2-Bromo-3-fluoroanilinepharmaceutical grade 2-Bromo-3-fluoroaniline2-Bromo-3-fluoroaniline priceagrochemical intermediates97% purity 2-Bromo-3-fluoroaniline

About 2-Bromo-3-fluoroaniline

2-Bromo-3-fluorophenylamine (CAS 111721-75-6) serves as a specialized building block within the API intermediates market, particularly for the synthesis of complex fluorinated aromatics used in oncology and antibacterial research. As CDMOs increasingly focus on precision medicine, there is a distinct shift toward sourc...

Synonyms

2-Bromo-3-fluoroaniline
111721-75-6
2-Bromo-3-fluorophenylamine
2-bromo-3-fluorobenzenamine
2-Bromo-3-fluoro-phenylamine

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2-Bromo-3-fluoroaniline Specifications

CAS Number

111721-75-6

Molecular Formula

C6H5BrFN

Molecular Weight

190.015 g/mol

IUPAC Name

2-bromo-3-fluoroaniline

Canonical SMILES

C1=CC(=C(C(=C1)F)Br)N

InChI Key

XZRSXRUYZXBTGD-UHFFFAOYSA-N

InChI

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

EINECS Number

676-172-1

MDL Number

MFCD07369915

HSN No

29214200

CAS Number

111721-75-6

Molecular Formula

C6H5BrFN

Molecular Weight

190.015 g/mol

IUPAC Name

2-bromo-3-fluoroaniline

Canonical SMILES

C1=CC(=C(C(=C1)F)Br)N

InChI Key

XZRSXRUYZXBTGD-UHFFFAOYSA-N

InChI

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

EINECS Number

676-172-1

MDL Number

MFCD07369915

HSN No

29214200

Molecular Weight

190.015 g/mol

Boiling Point

229.8±20.0 °C (Predicted)

Density

1.67 g/cm3

PSA

26 Å²

Average mass

190.01 g/mol

Monoisotopic mass

188.95894 Da

Molar mass

190.01 g/mol

Precautionary Statement Codes

P305+P351+P338

Hazard Classes and Categories

Acute Tox. 4 (13%), Acute Tox. 4 (13%), Skin Irrit. 2 (100%), Eye Irrit. 2 (100%), Acute Tox. 4 (13%), and STOT SE 3 (97.8%)

Pharmaceutical Intermediate

5-Bromo valeric acid serves as a versatile building block and critical intermediate in the synthesis of active pharmaceutical ingredients, including the development of drugs targeting neurological disorders and the construction of inhibitors for aminoglycoside-resistant bacteria

Organic Synthesis Reagent

This compound is extensively utilized in organic chemistry for the preparation of esters, amides, and sequence-specific base pair mimics as topoisomerase IB inhibitors, as well as in the construction of the alpha-chain of F2-alpha series prostaglandins

Material Science Building Block

It acts as a bifunctional ligand and precursor in the synthesis of specialized polymers, novel nanocarriers for photodynamic therapy, and semiconducting organic-inorganic nanocomposites.