2-Oxo-7-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)-2H-chromene-3-carboxylic acid
98%
Reagent
Code: #222233
CAS Number
1442461-73-5
blur_circular Chemical Specifications
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Molecular Information
Weight
316.11 g/mol
Formula
C₁₆H₁₇BO₆
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Registry Numbers
MDL Number
MFCD34186898
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Storage & Handling
Storage
2-8°C, dry
description Product Description
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active chromene derivatives. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research. Commonly employed in the development of fluorescent probes and optoelectronic materials due to the chromene backbone’s photophysical properties. Also applied in medicinal chemistry for constructing libraries of heterocyclic compounds with potential anticancer, antimicrobial, or anti-inflammatory activity.
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