2-Chloro-5-[(4-methylbenzenesulfonyl)methyl]-1,3-thiazole CAS 478032-39-2

Purity 97%+In StockPharmaceutical Standards
CAS No.478032-39-2
Molecular FormulaC11H10ClNO2S2
Molecular Weight287.79 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Chloro-5-[(4-methylbenzenesulfonyl)methyl]-1,3-thiazole CAS 478032-39-2 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

2-Chloro-5-[(4-methylbenzenesulfonyl)methyl]-1,3-thiazole (CAS 478032-39-2) is a high-purity analytical reference standard with the molecular formula C11H10ClNO2S2 and a molecular weight of 287.79 g/mol.

Structurally, 2-Chloro-5-[(4-methylbenzenesulfonyl)methyl]-1,3-thiazole (C11H10ClNO2S2) 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 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 287.79 g/mol, it falls into the medium-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO manufactures 2-Chloro-5-[(4-methylbenzenesulfonyl)methyl]-1,3-thiazole 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 FormulaC11H10ClNO2S2
Molecular Weight287.79 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms2

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