1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethanone
$216.00
CAS No.: 171364-81-1
Catalog No.: 188983
Purity: 95%
MF: C14H19BO3
MW: 246.115
Storage: 2-8 degree Celsius
SMILES: CC1(OB(OC1(C)C)C1=CC=C(C=C1)C(C)=O)C
Catalog No.: 188983
Purity: 95%
MF: C14H19BO3
MW: 246.115
Storage: 2-8 degree Celsius
SMILES: CC1(OB(OC1(C)C)C1=CC=C(C=C1)C(C)=O)C
For R&D use only. Not for human or animal use.
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![tert-butyl 2-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)-7-azaspiro[3.5]nonane-7-carboxylate](https://www.chemshuttle.com/media/catalog/product/cache/eda3e020a548044183bce7a8a96486f8/2/0/202747_5.jpg)
![tert-butyl 8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-azaspiro[4.5]dec-7-ene-2-carboxylate](https://www.chemshuttle.com/media/catalog/product/cache/eda3e020a548044183bce7a8a96486f8/2/0/202740.jpg)
1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethanone; CAS No.: 171364-81-1; 1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethanone is a boronate-substituted acetophenone. This compound represents a building block for introducing ketone groups via Suzuki couplings in drug discovery. ChemShuttle, a chemical synthesis company, specializes in supplying such boronate intermediates. Our custom synthesis team can create diverse aryl ketone derivatives. The tetramethyl dioxaborolane group facilitates cross-coupling reactions. We ensure high chemical purity to support your medicinal chemistry applications.
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