Tert-butyl 4-iodo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate CAS 945599-35-9

Purity 97%+In StockPharmaceutical Standards
CAS No.945599-35-9
Molecular FormulaC11H12IN3O2
Molecular Weight345.14 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl 4-iodo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate CAS 945599-35-9 chemical structure

Description

As a certified reference material (CRM), Tert-butyl 4-iodo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate 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.

Tert-butyl 4-iodo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate (CAS 945599-35-9) is a high-purity analytical reference standard with the molecular formula C11H12IN3O2 and a molecular weight of 345.14 g/mol.

Structurally, Tert-butyl 4-iodo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate (C11H12IN3O2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 345.14 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

Physical & Chemical Properties

Molecular FormulaC11H12IN3O2
Molecular Weight345.14 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentI-containing
Nitrogen Atoms3

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