tert-Butyl (2-chloro-4-(trifluoromethyl)thiophen-3-yl)carbamate CAS 2732241-85-7

Purity 97%+In StockPharmaceutical Standards
CAS No.2732241-85-7
Molecular FormulaC10H11ClF3NO2S
Molecular Weight301.71 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (2-chloro-4-(trifluoromethyl)thiophen-3-yl)carbamate CAS 2732241-85-7 chemical structure

Description

Based on its molecular formula C10H11ClF3NO2S, tert-Butyl (2-chloro-4-(trifluoromethyl)thiophen-3-yl)carbamate contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 301.71 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies tert-Butyl (2-chloro-4-(trifluoromethyl)thiophen-3-yl)carbamate (CAS 2732241-85-7), a certified reference material (molecular formula C10H11ClF3NO2S, MW 301.71 g/mol) for analytical method development and quality control.

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 tert-Butyl (2-chloro-4-(trifluoromethyl)thiophen-3-yl)carbamate 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 FormulaC10H11ClF3NO2S
Molecular Weight301.71 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2002
Halogen ContentF/Cl-containing
Nitrogen Atoms1
Sulfur Atoms1

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