tert-Butyl 3-Bromo-4-iodo-5-methylbenzoate CAS 2364584-56-3

Purity 97%+In StockPharmaceutical Standards
CAS No.2364584-56-3
Molecular FormulaC12H14BrIO2
Molecular Weight397.05 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 3-Bromo-4-iodo-5-methylbenzoate CAS 2364584-56-3 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including tert-Butyl 3-Bromo-4-iodo-5-methylbenzoate.

tert-Butyl 3-Bromo-4-iodo-5-methylbenzoate (CAS 2364584-56-3), molecular formula C12H14BrIO2 and molecular weight 397.05 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, tert-Butyl 3-Bromo-4-iodo-5-methylbenzoate (C12H14BrIO2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, bromine/iodine substitution, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 397.05 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.

CATO manufactures tert-Butyl 3-Bromo-4-iodo-5-methylbenzoate under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC12H14BrIO2
Molecular Weight397.05 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1999
Halogen ContentBr/I-containing

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