1,2,3,4-Tetrahydronaphthalene-2-carbothioamide CAS 58952-09-3

Purity 97%+In StockPharmaceutical Standards
CAS No.58952-09-3
Molecular FormulaC11H13NS
Molecular Weight191.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1,2,3,4-Tetrahydronaphthalene-2-carbothioamide CAS 58952-09-3 chemical structure

Description

The occurrence of 1,2,3,4-Tetrahydronaphthalene-2-carbothioamide is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 1,2,3,4-Tetrahydronaphthalene-2-carbothioamide (CAS 58952-09-3), a certified reference material (molecular formula C11H13NS, MW 191.29 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, 1,2,3,4-Tetrahydronaphthalene-2-carbothioamide is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 191.29 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.

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 1,2,3,4-Tetrahydronaphthalene-2-carbothioamide 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 FormulaC11H13NS
Molecular Weight191.29 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1973
Nitrogen Atoms1
Sulfur Atoms1

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