CAS 871332-94-4

Boronic acid,B-[3-[(butylamino)carbonyl]-4-chlorophenyl]-

Description:

Boronic acid, specifically the compound known as B-[3-[(butylamino)carbonyl]-4-chlorophenyl]- (CAS 871332-94-4), is characterized by its boron-containing functional group, which is typically represented as -B(OH)2. This compound features a chlorophenyl ring, which contributes to its aromatic properties and potential reactivity. The presence of a butylamino group indicates that it has an amine functionality, which can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Boronic acids are known for their ability to form reversible complexes with diols, making them useful in organic synthesis and materials science. Additionally, this compound may exhibit biological activity due to its structural components, which can interact with biological targets. Its solubility and stability in different solvents can vary, influencing its application in synthetic chemistry and medicinal chemistry. Overall, this boronic acid derivative is a versatile compound with potential applications in drug development and organic synthesis.

Formula: C₁₁H₁₅BClNO₃

Synonyms:

• Boronicacid, [3-[(butylamino)carbonyl]-4-chlorophenyl]- (9CI)

4-CHLORO-3-(N-BUTYLAMINOCARBONYL)PHENYLBORONIC ACID

CAS: 871332-94-4

Formula: C₁₁H₁₅BClNO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 255.5057

Ref: IN-DA004TVC

4-Chloro-3-(N-butylaminocarbonyl)phenylboronic acid

CAS: 871332-94-4

4-Chloro-3-(N-butylaminocarbonyl)phenylboronic acid

Purity: ≥95%

Molecular weight: 255.51g/mol

Ref: 54-OR360066

(3-(Butylcarbamoyl)-4-chlorophenyl)boronic acid

CAS: 871332-94-4

Formula: C₁₁H₁₅BClNO₃

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 255.51

Ref: 10-F215887