CAS 276669-74-0: {3-[(trichloroacetyl)amino]phenyl}boronic acid

Description: {3-[(Trichloroacetyl)amino]phenyl}boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a trichloroacetylamino group. This compound typically exhibits properties such as being a solid at room temperature, with potential solubility in polar organic solvents. The trichloroacetyl group contributes to its reactivity, particularly in nucleophilic substitution reactions, while the boronic acid moiety allows for participation in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of chlorine atoms enhances its electrophilicity, which can influence its interaction with biological targets. Additionally, boronic acids are known for their ability to form reversible covalent bonds with diols, which can be exploited in various applications, including drug delivery and sensor development. Overall, this compound's unique structural features and functional groups make it a versatile building block in chemical research and development.

Formula: C₈H₇BCl₃NO₃

InChI: InChI=1/C8H7BCl3NO3/c10-8(11,12)7(14)13-6-3-1-2-5(4-6)9(15)16/h1-4,15-16H,(H,13,14)

Boronic acid, [3-[(trichloroacetyl)amino]phenyl]- (9CI)

CAS: 276669-74-0

• Formula: C₈H₇BCl₃NO₃
• Color and Shape: Solid
• Molecular weight: 282.3161

3-(2,2,2-Trichloroacetamido)benzeneboronic acid

CAS: 276669-74-0

• Purity: 97%
• Molecular weight: 282.32g/mol

3-(2,2,2-Trichloroacetamido)phenylboronic acid

CAS: 276669-74-0

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• Formula: C₈H₇BCl₃NO₃
• Purity: Min. 95%
• Molecular weight: 282.32 g/mol