1256358-59-4 | 3-(Thiomorpholin-4-ylmethyl)phenylboronic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	1 week	$263.00	$184.00
500mg	95%	1 week	$354.00	$248.00
1g	95%	1 week	$476.00	$333.00

Description

• Catalog Number: AA31107
• Chemical Name: 3-(Thiomorpholin-4-ylmethyl)phenylboronic acid
• CAS Number: 1256358-59-4
• Molecular Formula: C11H16BNO2S
• Molecular Weight: 237.1262
• MDL Number: MFCD14687174
• SMILES: OB(c1cccc(c1)CN1CCSCC1)O

Computed Properties

• Complexity: 212
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3

Upstream Synthesis Route

The (3-(Thiomorpholinomethyl)phenyl)boronic acid is a versatile compound used in various chemical synthesis processes. Its unique structure containing a boronic acid group attached to a thiomorpholine ring and a phenyl group offers several important applications in organic chemistry, particularly in the formation of carbon-carbon and carbon-heteroatom bonds.One key application of (3-(Thiomorpholinomethyl)phenyl)boronic acid is in Suzuki-Miyaura cross-coupling reactions. In this process, the boronic acid group undergoes a palladium-catalyzed coupling reaction with an organic halide or pseudohalide, resulting in the formation of a new carbon-carbon bond. This reaction is widely used in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials science.Additionally, the thiomorpholine ring in the structure of the compound provides an opportunity for sulfur incorporation into organic molecules. This feature is advantageous for the construction of sulfur-containing compounds, which are of interest in medicinal chemistry and materials science.Overall, the (3-(Thiomorpholinomethyl)phenyl)boronic acid serves as a valuable building block in organic synthesis, enabling the creation of diverse and structurally complex molecules through efficient bond-forming reactions.