1-[4-(2-Fluorophenyl)-1,3-thiazol-2-yl]-4-(thiophen-3-yl)-1H-pyrazol-5-amine CAS 955967-08-5

Purity 97%+In StockPharmaceutical Standards
CAS No.955967-08-5
Molecular FormulaC16H11FN4S2
Molecular Weight342.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-[4-(2-Fluorophenyl)-1,3-thiazol-2-yl]-4-(thiophen-3-yl)-1H-pyrazol-5-amine CAS 955967-08-5 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies 1-[4-(2-Fluorophenyl)-1,3-thiazol-2-yl]-4-(thiophen-3-yl)-1H-pyrazol-5-amine (CAS 955967-08-5), a certified reference material (molecular formula C16H11FN4S2, MW 342.41 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, fluorine substitution, 1-[4-(2-Fluorophenyl)-1,3-thiazol-2-yl]-4-(thiophen-3-yl)-1H-pyrazol-5-amine is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 342.41 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures 1-[4-(2-Fluorophenyl)-1,3-thiazol-2-yl]-4-(thiophen-3-yl)-1H-pyrazol-5-amine 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 FormulaC16H11FN4S2
Molecular Weight342.41 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)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms4
Sulfur Atoms2

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