5-chloro-3-iodo-1-(²H₃)methyl-1H-pyrazolo[4,3-d]pyrimidine CAS 2564785-56-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2564785-56-2
Molecular Formula-
Molecular Weight297.50 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-chloro-3-iodo-1-(²H₃)methyl-1H-pyrazolo[4,3-d]pyrimidine CAS 2564785-56-2 chemical structure

Description

5-chloro-3-iodo-1-(²H₃)methyl-1H-pyrazolo[4,3-d]pyrimidine (C6HD3ClIN4) contains deuterium isotope labeling, a nitrile group, chlorine/iodine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO supplies 5-chloro-3-iodo-1-(²H₃)methyl-1H-pyrazolo[4,3-d]pyrimidine (CAS 2564785-56-2), a certified reference material (molecular formula C6HD3ClIN4, MW 297.50 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC6HD3ClIN4
Molecular Weight297.50 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2001
Halogen ContentCl/I-containing
Nitrogen Atoms4

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