1-Bromo-3-fluoro-2-iodo-5-(trifluoromethyl)benzene CAS 1934724-90-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1934724-90-9
Molecular FormulaC7H2BrF4I
Molecular Weight368.89 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Bromo-3-fluoro-2-iodo-5-(trifluoromethyl)benzene CAS 1934724-90-9 chemical structure

Description

The occurrence of 1-Bromo-3-fluoro-2-iodo-5-(trifluoromethyl)benzene is closely related to fluorine/bromine/iodine substitution, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

1-Bromo-3-fluoro-2-iodo-5-(trifluoromethyl)benzene (CAS 1934724-90-9), molecular formula C7H2BrF4I and molecular weight 368.89 g/mol, is a CATO reference standard with documented purity and traceability.

1-Bromo-3-fluoro-2-iodo-5-(trifluoromethyl)benzene (C7H2BrF4I) contains fluorine/bromine/iodine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 1-Bromo-3-fluoro-2-iodo-5-(trifluoromethyl)benzene meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC7H2BrF4I
Molecular Weight368.89 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in methanol, acetonitrile, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1996
Halogen ContentF/Br/I-containing

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