tert-Butyl 3-iodo-1H-thieno[3,2-c]pyrazole-1-carboxylate CAS 848356-70-7

Purity 97%+In StockPharmaceutical Standards
CAS No.848356-70-7
Molecular FormulaC10H11IN2O2S
Molecular Weight350.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 3-iodo-1H-thieno[3,2-c]pyrazole-1-carboxylate CAS 848356-70-7 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, iodine substitution, tert-Butyl 3-iodo-1H-thieno[3,2-c]pyrazole-1-carboxylate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 350.18 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

tert-Butyl 3-iodo-1H-thieno[3,2-c]pyrazole-1-carboxylate (CAS 848356-70-7), molecular formula C10H11IN2O2S and molecular weight 350.18 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.

CATO manufactures tert-Butyl 3-iodo-1H-thieno[3,2-c]pyrazole-1-carboxylate under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC10H11IN2O2S
Molecular Weight350.18 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentI-containing
Nitrogen Atoms2
Sulfur Atoms1

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