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-fluoroaniline (CAS 111721-75-6) is experiencing significant demand within the United States API intermediates market as pharmaceutical manufacturers prioritize high purity fine chemicals with a minimum Pharma/API purity of 99% to ensure the integrity of downstream oncology and CNS therapeutic pipelines. 2-bro...

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.