3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopentanone
$450.00
CAS No.: 134892-21-0
Catalog No.: 172012
Purity: 95%
MF: C11H19BO3
MW: 210.082
Storage: 2-8 degree Celsius
SMILES: CC1(C)OB(OC1(C)C)C1CCC(=O)C1
Catalog No.: 172012
Purity: 95%
MF: C11H19BO3
MW: 210.082
Storage: 2-8 degree Celsius
SMILES: CC1(C)OB(OC1(C)C)C1CCC(=O)C1
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)
3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopentanone; CAS No.: 134892-21-0; As a Chemical Online Mall, ChemShuttle offers 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopentanone. This boron-containing cyclopentanone serves as a building block for Suzuki-Miyaura cross-couplings in strained ring system synthesis. The cyclopentanone ring enables subsequent aldol reactions or reductive aminations after boronate coupling. Applications include prostaglandin analog synthesis and strained hydrocarbon materials. The online platform provides real-time access to coupling reaction optimization data. Custom services include preparation of enantiomerically pure substrates using asymmetric catalysis.
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