Methyl 3-((2-amino-5-fluorobenzyl)oxy)-4-bromobenzoate CAS 1956382-12-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1956382-12-9
Molecular FormulaC15H13BrFNO3
Molecular Weight354.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-((2-amino-5-fluorobenzyl)oxy)-4-bromobenzoate CAS 1956382-12-9 chemical structure

Description

As a certified reference material (CRM), Methyl 3-((2-amino-5-fluorobenzyl)oxy)-4-bromobenzoate 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.

CATO supplies Methyl 3-((2-amino-5-fluorobenzyl)oxy)-4-bromobenzoate (CAS 1956382-12-9), a certified reference material (molecular formula C15H13BrFNO3, MW 354.17 g/mol) for analytical method development and quality control.

Structurally, Methyl 3-((2-amino-5-fluorobenzyl)oxy)-4-bromobenzoate (C15H13BrFNO3) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 354.17 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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

Physical & Chemical Properties

Molecular FormulaC15H13BrFNO3
Molecular Weight354.17 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1996
Halogen ContentF/Br-containing
Nitrogen Atoms1

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