Methyl 4-amino-2-(4-(4-chlorophenyl)piperazin-1-yl)thiazole-5-carboxylate CAS 343375-62-2

Purity 97%+In StockPharmaceutical Standards
CAS No.343375-62-2
Molecular FormulaC15H17ClN4O2S
Molecular Weight352.84 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 4-amino-2-(4-(4-chlorophenyl)piperazin-1-yl)thiazole-5-carboxylate CAS 343375-62-2 chemical structure

Description

CATO manufactures Methyl 4-amino-2-(4-(4-chlorophenyl)piperazin-1-yl)thiazole-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.

Methyl 4-amino-2-(4-(4-chlorophenyl)piperazin-1-yl)thiazole-5-carboxylate (CAS 343375-62-2) is a high-purity analytical reference standard with the molecular formula C15H17ClN4O2S and a molecular weight of 352.84 g/mol.

Structurally, Methyl 4-amino-2-(4-(4-chlorophenyl)piperazin-1-yl)thiazole-5-carboxylate (C15H17ClN4O2S) 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 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 352.84 g/mol, it falls into the moderately-high-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 FormulaC15H17ClN4O2S
Molecular Weight352.84 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms4
Sulfur Atoms1

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