(1R,2R,6S,8R)-2,9,9-trimethyl-4-phenyl-3,5-dioxa-4-boratricyclo[6.1.1.0²,6]decane

Product Name (1R,2R,6S,8R)-2,9,9-trimethyl-4-phenyl-3,5-dioxa-4-boratricyclo[6.1.1.0²,6]decane
CAT No. CS-EL-00333
CAS No. 76110-78-6
Category Impurities
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Canonical Smiles B1(OC2CC3CC(C3(C)C)C2(O1)C)C4=CC=CC=C4
InchIKey OZQWJKOXOILFRR-ZIEJDFEHSA-N
Inchl InChI=1S/C16H21BO2/c1-15(2)11-9-13(15)16(3)14(10-11)18-17(19-16)12-7-5-4-6-8-12/h4-8,11,13-14H,9-10H2,1-3H3/t11-,13-,14+,16-/m0/s1
IUPAC (1S,2S,6R,8S)-2,9,9-trimethyl-4-phenyl-3,5-dioxa-4-boratricyclo[6.1.1.02,6]decane
Controlled No
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(1R,2R,6S,8R)-2,9,9-trimethyl-4-phenyl-3,5-dioxa-4-boratricyclo[6.1.1.0²,6]decane, also known as Boronate BAPTA, is a chemical compound that is commonly used in biochemical research as a chelator for the measurement of intracellular calcium concentrations. Boronate BAPTA is a large, asymmetric molecule that contains two boron atoms, which are critical for its chelating properties. The compound is highly water-soluble and can be easily incorporated into cells using various delivery methods, such as microinjection or electroporation. Once inside the cell, Boronate BAPTA binds with calcium ions, forming a stable complex that can be measured using fluorescence or absorbance spectroscopy. This complex formation allows researchers to monitor changes in intracellular calcium concentrations in real-time

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