Methyl 6-bromo-1,2,3,4-tetrahydroquinoline-4-carboxylate CAS 1508913-34-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1508913-34-5
Molecular FormulaC11H12BrNO2
Molecular Weight270.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 6-bromo-1,2,3,4-tetrahydroquinoline-4-carboxylate CAS 1508913-34-5 chemical structure

Description

CATO manufactures Methyl 6-bromo-1,2,3,4-tetrahydroquinoline-4-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.

Methyl 6-bromo-1,2,3,4-tetrahydroquinoline-4-carboxylate (CAS 1508913-34-5) is a high-purity analytical reference standard with the molecular formula C11H12BrNO2 and a molecular weight of 270.12 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution, Methyl 6-bromo-1,2,3,4-tetrahydroquinoline-4-carboxylate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 270.12 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 FormulaC11H12BrNO2
Molecular Weight270.12 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentBr-containing
Nitrogen Atoms1

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