(1,1-Dioxidonaphtho[1,2-b]thiophen-2-yl)methyl carbonochloridate CAS 931114-43-1

Purity 97%+In StockPharmaceutical Standards
CAS No.931114-43-1
Molecular FormulaC14H9ClO4S
Molecular Weight308.74 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1,1-Dioxidonaphtho[1,2-b]thiophen-2-yl)methyl carbonochloridate CAS 931114-43-1 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 (1,1-Dioxidonaphtho[1,2-b]thiophen-2-yl)methyl carbonochloridate (CAS 931114-43-1), a certified reference material (molecular formula C14H9ClO4S, MW 308.74 g/mol) for analytical method development and quality control.

Owing to a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, a polycyclic aromatic system, (1,1-Dioxidonaphtho[1,2-b]thiophen-2-yl)methyl carbonochloridate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 308.74 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 (1,1-Dioxidonaphtho[1,2-b]thiophen-2-yl)methyl carbonochloridate 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 FormulaC14H9ClO4S
Molecular Weight308.74 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Sulfur Atoms1

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