1-Methyl-1,2,3,4-tetrahydroquinoline-6-carbonyl chloride CAS 32565-01-8

Purity 97%+In StockPharmaceutical Standards
CAS No.32565-01-8
Molecular FormulaC11H12ClNO
Molecular Weight209.67 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Methyl-1,2,3,4-tetrahydroquinoline-6-carbonyl chloride CAS 32565-01-8 chemical structure

Description

CATO manufactures 1-Methyl-1,2,3,4-tetrahydroquinoline-6-carbonyl chloride 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 1-Methyl-1,2,3,4-tetrahydroquinoline-6-carbonyl chloride (CAS 32565-01-8), a certified reference material (molecular formula C11H12ClNO, MW 209.67 g/mol) for analytical method development and quality control.

Based on its molecular formula C11H12ClNO, 1-Methyl-1,2,3,4-tetrahydroquinoline-6-carbonyl chloride contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 209.67 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC11H12ClNO
Molecular Weight209.67 g/mol
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
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1966
Halogen ContentCl-containing
Nitrogen Atoms1

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