2-Boc-5-(2-Isopropylamino-thiazol-4-yl) -isoindoline CAS 850877-62-2

Purity 97%+In StockPharmaceutical Standards
CAS No.850877-62-2
Molecular FormulaC19H25N3O2S
Molecular Weight359.49 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Boc-5-(2-Isopropylamino-thiazol-4-yl) -isoindoline CAS 850877-62-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 359.49 g/mol gives 2-Boc-5-(2-Isopropylamino-thiazol-4-yl) -isoindoline distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 2-Boc-5-(2-Isopropylamino-thiazol-4-yl) -isoindoline (CAS 850877-62-2), a certified reference material (molecular formula C19H25N3O2S, MW 359.49 g/mol) for analytical method development and quality control.

Based on its molecular formula C19H25N3O2S, 2-Boc-5-(2-Isopropylamino-thiazol-4-yl) -isoindoline contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 359.49 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

As a certified reference material (CRM), 2-Boc-5-(2-Isopropylamino-thiazol-4-yl) -isoindoline meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC19H25N3O2S
Molecular Weight359.49 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
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms3
Sulfur Atoms1

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