2,6-dihydro-2-(4-iodophenyl)-4H-Thieno[3,4-c]pyrazol-3-amine CAS 1418273-61-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1418273-61-6
Molecular FormulaC11H10IN3S
Molecular Weight343.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,6-dihydro-2-(4-iodophenyl)-4H-Thieno[3,4-c]pyrazol-3-amine CAS 1418273-61-6 chemical structure

Description

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 supplies 2,6-dihydro-2-(4-iodophenyl)-4H-Thieno[3,4-c]pyrazol-3-amine (CAS 1418273-61-6), a certified reference material (molecular formula C11H10IN3S, MW 343.19 g/mol) for analytical method development and quality control.

Based on its molecular formula C11H10IN3S, 2,6-dihydro-2-(4-iodophenyl)-4H-Thieno[3,4-c]pyrazol-3-amine contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, iodine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 343.19 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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), 2,6-dihydro-2-(4-iodophenyl)-4H-Thieno[3,4-c]pyrazol-3-amine 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 FormulaC11H10IN3S
Molecular Weight343.19 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentI-containing
Nitrogen Atoms3
Sulfur Atoms1

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