CAS 148355-75-3: 3-(Methanesulfonylamino)phenylboronic acid

Description: 3-(Methanesulfonylamino)phenylboronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with a methanesulfonylamino group, enhancing its solubility and reactivity. The methanesulfonylamino moiety contributes to its potential as a versatile building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The boronic acid functionality allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the formation of carbon-carbon bonds. Additionally, this compound may exhibit properties such as moderate stability under standard conditions, but it can be sensitive to moisture and air, necessitating careful handling and storage. Its applications extend to medicinal chemistry, where it may serve as a lead compound or intermediate in the synthesis of biologically active molecules. Overall, 3-(Methanesulfonylamino)phenylboronic acid is a significant compound in the field of organic chemistry with diverse applications.

Formula: C₇H₁₀BNO₄S

InChI: InChI=1/C7H10BNO4S/c1-14(12,13)9-7-4-2-3-6(5-7)8(10)11/h2-5,9-11H,1H3

Synonyms:

• {3-[(Methylsulfonyl)Amino]Phenyl}Boronic Acid

Boronic acid, B-[3-[(methylsulfonyl)amino]phenyl]-

CAS: 148355-75-3

• Formula: C₇H₁₀BNO₄S
• Purity: 98%
• Color and Shape: Solid
• Molecular weight: 215.0346

3-[(Methylsulphonyl)amino]benzeneboronic acid

CAS: 148355-75-3

• Formula: C₇H₁₀BNO₄S
• Purity: 98%
• Color and Shape: beige solid
• Molecular weight: 215.03g/mol

3-(Methylsulfonylamino)phenylboronic acid

CAS: 148355-75-3

• Purity: 97.0%
• Color and Shape: Solid
• Molecular weight: 215.02999877929688

3-Methylsulfonylaminophenylboronic acid

CAS: 148355-75-3

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• Formula: C₇H₁₀BNO₄S
• Purity: Min. 95%
• Molecular weight: 215.04 g/mol