(1-(tert-butoxycarbonyl)-6-((tert-butyldimethylsilyl)oxy)-1H-indol-2-yl)boronic acid CAS 848357-99-3

Purity 97%+In StockPharmaceutical Standards
CAS No.848357-99-3
Molecular FormulaC19H30BNO5Si
Molecular Weight391.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1-(tert-butoxycarbonyl)-6-((tert-butyldimethylsilyl)oxy)-1H-indol-2-yl)boronic acid CAS 848357-99-3 chemical structure

Description

(1-(tert-butoxycarbonyl)-6-((tert-butyldimethylsilyl)oxy)-1H-indol-2-yl)boronic acid (C19H30BNO5Si) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. The carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

(1-(tert-butoxycarbonyl)-6-((tert-butyldimethylsilyl)oxy)-1H-indol-2-yl)boronic acid (CAS 848357-99-3), molecular formula C19H30BNO5Si and molecular weight 391.34 g/mol, is a CATO reference standard with documented purity and traceability.

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-(tert-butoxycarbonyl)-6-((tert-butyldimethylsilyl)oxy)-1H-indol-2-yl)boronic acid 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 FormulaC19H30BNO5Si
Molecular Weight391.34 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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