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Home  > Chemistry  > Heterocyclic Building Blocks  > Thiophenes  > 5-(1-Piperidinylmethyl)thiophene-2-boronic acid pinacol ester

AA54539

1218790-44-3 | 5-(1-Piperidinylmethyl)thiophene-2-boronic acid pinacol ester

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 -   +

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*All prices are in USD.

Description
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

 

Computed Properties
Complexity: 355  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 21  
Hydrogen Bond Acceptor Count: 4  
Rotatable Bond Count: 3  

 

 

Upstream Synthesis Route
  • 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.
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