7-(Hydroxymethyl)-3-methyl-5h-[1,3]thiazolo[3,2-a]pyrimidin-5-one CAS 926257-63-8

Purity 97%+In StockPharmaceutical Standards
CAS No.926257-63-8
Molecular FormulaC8H8N2O2S
Molecular Weight196.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

7-(Hydroxymethyl)-3-methyl-5h-[1,3]thiazolo[3,2-a]pyrimidin-5-one CAS 926257-63-8 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.

7-(Hydroxymethyl)-3-methyl-5h-[1,3]thiazolo[3,2-a]pyrimidin-5-one (CAS 926257-63-8) is a high-purity analytical reference standard with the molecular formula C8H8N2O2S and a molecular weight of 196.23 g/mol.

Structurally, 7-(Hydroxymethyl)-3-methyl-5h-[1,3]thiazolo[3,2-a]pyrimidin-5-one (C8H8N2O2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 196.23 g/mol, it falls into the medium-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.

As a certified reference material (CRM), 7-(Hydroxymethyl)-3-methyl-5h-[1,3]thiazolo[3,2-a]pyrimidin-5-one 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 FormulaC8H8N2O2S
Molecular Weight196.23 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms2
Sulfur Atoms1

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