3-Chloro-N-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide CAS 2271133-59-4

Purity 97%+In StockPharmaceutical Standards
CAS No.2271133-59-4
Molecular FormulaC14H19BClNO3
Molecular Weight295.57 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Chloro-N-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide CAS 2271133-59-4 chemical structure

Description

The molecular framework of 3-Chloro-N-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (C14H19BClNO3) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 3-Chloro-N-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (CAS 2271133-59-4), a certified reference material (molecular formula C14H19BClNO3, MW 295.57 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 3-Chloro-N-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide 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 FormulaC14H19BClNO3
Molecular Weight295.57 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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)5.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1998
Halogen ContentCl-containing
Nitrogen Atoms1

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