Ethyl 2-iodo-4-methyloxazole-5-carboxylate CAS 78451-12-4

Purity 97%+In StockPharmaceutical Standards
CAS No.78451-12-4
Molecular FormulaC7H8INO3
Molecular Weight281.05 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 2-iodo-4-methyloxazole-5-carboxylate CAS 78451-12-4 chemical structure

Description

CATO manufactures Ethyl 2-iodo-4-methyloxazole-5-carboxylate 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.

CATO supplies Ethyl 2-iodo-4-methyloxazole-5-carboxylate (CAS 78451-12-4), a certified reference material (molecular formula C7H8INO3, MW 281.05 g/mol) for analytical method development and quality control.

Structurally, Ethyl 2-iodo-4-methyloxazole-5-carboxylate (C7H8INO3) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 281.05 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC7H8INO3
Molecular Weight281.05 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO, water
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1979
Halogen ContentI-containing
Nitrogen Atoms1

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