6-(tert-Butyl)-2-(2-furoylamino)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic acid CAS 407587-33-1

Purity 97%+In StockPharmaceutical Standards
CAS No.407587-33-1
Molecular FormulaC18H21NO4S
Molecular Weight347.43 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-(tert-Butyl)-2-(2-furoylamino)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic acid CAS 407587-33-1 chemical structure

Description

CATO manufactures 6-(tert-Butyl)-2-(2-furoylamino)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic 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.

CATO supplies 6-(tert-Butyl)-2-(2-furoylamino)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic acid (CAS 407587-33-1), a certified reference material (molecular formula C18H21NO4S, MW 347.43 g/mol) for analytical method development and quality control.

Owing to a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, 6-(tert-Butyl)-2-(2-furoylamino)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic acid is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 347.43 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).

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.

Physical & Chemical Properties

Molecular FormulaC18H21NO4S
Molecular Weight347.43 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms1
Sulfur Atoms1

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