(1-(Tert-butyldimethylsilyl)-1H-indol-6-yl)boronic acid CAS 913835-60-6

Purity 97%+In StockPharmaceutical Standards
CAS No.913835-60-6
Molecular FormulaC14H22BNO2Si
Molecular Weight275.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1-(Tert-butyldimethylsilyl)-1H-indol-6-yl)boronic acid CAS 913835-60-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 275.23 g/mol gives (1-(Tert-butyldimethylsilyl)-1H-indol-6-yl)boronic acid distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies (1-(Tert-butyldimethylsilyl)-1H-indol-6-yl)boronic acid (CAS 913835-60-6), a certified reference material (molecular formula C14H22BNO2Si, MW 275.23 g/mol) for analytical method development and quality control.

(1-(Tert-butyldimethylsilyl)-1H-indol-6-yl)boronic acid (C14H22BNO2Si) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC14H22BNO2Si
Molecular Weight275.23 g/mol
AppearanceOff-white to pale yellow crystalline powder
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
Degree of Unsaturation (DBE)4.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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