5-(2-furyl)-2H-1,2,6-thiadiazine-3-carboxylic acid 1,1-dioxide CAS 1011397-87-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1011397-87-7
Molecular FormulaC8H6N2O5S
Molecular Weight242.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(2-furyl)-2H-1,2,6-thiadiazine-3-carboxylic acid 1,1-dioxide CAS 1011397-87-7 chemical structure

Description

The molecular framework of 5-(2-furyl)-2H-1,2,6-thiadiazine-3-carboxylic acid 1,1-dioxide (C8H6N2O5S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

5-(2-furyl)-2H-1,2,6-thiadiazine-3-carboxylic acid 1,1-dioxide (CAS 1011397-87-7), molecular formula C8H6N2O5S and molecular weight 242.21 g/mol, is a CATO reference standard with documented purity and traceability.

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 5-(2-furyl)-2H-1,2,6-thiadiazine-3-carboxylic acid 1,1-dioxide 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 FormulaC8H6N2O5S
Molecular Weight242.21 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms2
Sulfur Atoms1

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