(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-3-yl)methanol
$392.00
CAS No.: 1310384-43-0
Catalog No.: 125704
Purity: 95%
MF: C11H17BO3S
MW: 240.133
Storage: 2-8 degree Celsius
SMILES: CC1(C)OB(OC1(C)C)C1=C(CO)C=CS1
Catalog No.: 125704
Purity: 95%
MF: C11H17BO3S
MW: 240.133
Storage: 2-8 degree Celsius
SMILES: CC1(C)OB(OC1(C)C)C1=C(CO)C=CS1
For R&D use only. Not for human or veterinary use.
![4,4,5,5-tetramethyl-2-(1,4-dioxaspiro[4.5]dec-7-en-8-yl)-1,3,2-dioxaborolane](https://www.chemshuttle.com/media/catalog/product/cache/eda3e020a548044183bce7a8a96486f8/1/0/102227_6.jpg)
![1-(tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazolo[3,4-b]pyridine-3-carbaldehyde](https://www.chemshuttle.com/media/catalog/product/cache/eda3e020a548044183bce7a8a96486f8/1/0/100225_5.jpg)
(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-3-yl)methanol; CAS No.: 1310384-43-0; This thiophene boronate ester highlights our capabilities in heteroaromatic Suzuki coupling partners. The benzyl alcohol substituent enables subsequent oxidation to ketones or conjugation via ester linkages. ChemShuttle's expertise in protecting group strategies ensures compatibility with diverse reaction conditions in medicinal chemistry workflows.
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