3-iodo-6-methoxy-1-methyl-pyrazolo[3,4-d]pyrimidine CAS 2919774-43-7

Purity 97%+In StockPharmaceutical Standards
CAS No.2919774-43-7
Molecular FormulaC7H7IN4O
Molecular Weight290.06 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-iodo-6-methoxy-1-methyl-pyrazolo[3,4-d]pyrimidine CAS 2919774-43-7 chemical structure

Description

3-iodo-6-methoxy-1-methyl-pyrazolo[3,4-d]pyrimidine (C7H7IN4O) contains an amide group, a hydroxyl group, an ether linkage, 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

3-iodo-6-methoxy-1-methyl-pyrazolo[3,4-d]pyrimidine (CAS 2919774-43-7), molecular formula C7H7IN4O and molecular weight 290.06 g/mol, is a CATO reference standard with documented purity and traceability.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), 3-iodo-6-methoxy-1-methyl-pyrazolo[3,4-d]pyrimidine 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 FormulaC7H7IN4O
Molecular Weight290.06 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2004
Halogen ContentI-containing
Nitrogen Atoms4

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