CAS 252663-48-2: 4-(Butylaminocarbonyl)phenylboronic acid

Description: 4-(Butylaminocarbonyl)phenylboronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with a butylaminocarbonyl group. This compound typically exhibits properties associated with both boronic acids and amides, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as drug development and materials science. The boronic acid moiety allows for participation in Suzuki coupling reactions, which are valuable in organic synthesis for forming carbon-carbon bonds. Additionally, the butylaminocarbonyl group contributes to the compound's solubility and reactivity, influencing its interaction with biological systems. The compound is likely to be a solid at room temperature, with moderate stability under standard conditions, although it may be sensitive to moisture due to the presence of the boronic acid group. Overall, 4-(Butylaminocarbonyl)phenylboronic acid is a versatile compound with potential applications in medicinal chemistry and organic synthesis.

Formula: C₁₁H₁₆BNO₃

InChI: InChI=1/C11H16BNO3/c1-2-3-8-13-11(14)9-4-6-10(7-5-9)12(15)16/h4-7,15-16H,2-3,8H2,1H3,(H,13,14)

Synonyms:

• [4-(Butylcarbamoyl)Phenyl]Boronic Acid

4-(BUTYLAMINOCARBONYL)PHENYLBORONIC ACID

CAS: 252663-48-2

• Formula: C₁₁H₁₆BNO₃
• Purity: 95%
• Color and Shape: Solid
• Molecular weight: 221.0606

4-(Butylcarbamoyl)benzeneboronic acid

CAS: 252663-48-2

• Formula: C₁₁H₁₆BNO₃
• Purity: By hplc: 99.5% (Typical Value in Batch COA)
• Color and Shape: white solid
• Molecular weight: 221.06g/mol

(4-(Butylcarbamoyl)phenyl)boronic acid

CAS: 252663-48-2

• Purity: 95.0%
• Molecular weight: 221.05999755859375

4-[(ButylaMino)carbonyl]phenyl]boronic acid

CAS: 252663-48-2

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• Formula: CHBNO
• Purity: Min. 95%
• Molecular weight: 221.06 g/mol