AA54539
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 96% | in stock | $66.00 | $47.00 | - + | |
5g | 96% | in stock | $235.00 | $165.00 | - + | |
10g | 96% | in stock | $387.00 | $271.00 | - + | |
25g | 96% | in stock | $667.00 | $467.00 | - + | |
100g | 96% | in stock | $2,004.00 | $1,403.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA54539 |
Chemical Name: | 5-(1-Piperidinylmethyl)thiophene-2-boronic acid pinacol ester |
CAS Number: | 1218790-44-3 |
Molecular Formula: | C16H26BNO2S |
Molecular Weight: | 307.2591 |
MDL Number: | MFCD11113036 |
SMILES: | CC1(C)OB(OC1(C)C)c1ccc(s1)CN1CCCCC1 |
Complexity: | 355 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 21 |
Hydrogen Bond Acceptor Count: | 4 |
Rotatable Bond Count: | 3 |
The compound 1-((5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl)methyl)piperidine plays a crucial role in chemical synthesis as a versatile building block. Its unique structure contains a boronate ester and a heterocyclic ring which are valuable functional groups in organic chemistry. This compound can be utilized as a key intermediate in the synthesis of various complex organic molecules due to its ability to undergo diverse reactions such as cross-coupling reactions, Suzuki-Miyaura coupling, and palladium-catalyzed processes. In addition, the piperidine moiety enhances the compound's reactivity and provides opportunities for further functionalization. With its potential applications in medicinal chemistry, materials science, and drug discovery, this compound holds promise for the development of novel compounds with enhanced properties and functionalities.