8-methanesulfonyl-1,2,3,4-tetrahydroquinoline hydrochloride CAS 1909325-08-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1909325-08-1
Molecular FormulaC10H13NO2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

8-methanesulfonyl-1,2,3,4-tetrahydroquinoline hydrochloride CAS 1909325-08-1 chemical structure

Description

Structurally, 8-methanesulfonyl-1,2,3,4-tetrahydroquinoline hydrochloride (C10H13NO2SHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. 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 247.74 g/mol, it falls into the medium-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies 8-methanesulfonyl-1,2,3,4-tetrahydroquinoline hydrochloride (CAS 1909325-08-1), a certified reference material (molecular formula C10H13NO2SHCl, MW 247.74 g/mol) for analytical method development and quality control.

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 8-methanesulfonyl-1,2,3,4-tetrahydroquinoline hydrochloride 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 FormulaC10H13NO2S HCl
Molecular Weight247.74 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; 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.)1995
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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