2-(((5-((3-Fluorophenyl)carbamoyl)-1,3,4-thiadiazol-2-yl)methyl)thio)acetic acid CAS 1142209-68-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1142209-68-4
Molecular FormulaC12H10FN3O3S2
Molecular Weight327.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(((5-((3-Fluorophenyl)carbamoyl)-1,3,4-thiadiazol-2-yl)methyl)thio)acetic acid CAS 1142209-68-4 chemical structure

Description

CATO supplies 2-(((5-((3-Fluorophenyl)carbamoyl)-1,3,4-thiadiazol-2-yl)methyl)thio)acetic acid (CAS 1142209-68-4), a certified reference material (molecular formula C12H10FN3O3S2, MW 327.35 g/mol) for analytical method development and quality control.

Structurally, 2-(((5-((3-Fluorophenyl)carbamoyl)-1,3,4-thiadiazol-2-yl)methyl)thio)acetic acid (C12H10FN3O3S2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 327.35 g/mol, it falls into the moderately-high-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

CATO manufactures 2-(((5-((3-Fluorophenyl)carbamoyl)-1,3,4-thiadiazol-2-yl)methyl)thio)acetic acid 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 FormulaC12H10FN3O3S2
Molecular Weight327.35 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms2

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