CAS 2121511-41-7: B-(2,5-Dichloro-3-fluorophenyl)boronic acid

Description: B-(2,5-Dichloro-3-fluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with two chlorine atoms and one fluorine atom. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of halogen substituents can influence its reactivity, solubility, and biological activity. Generally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. Additionally, the specific substitutions on the phenyl ring can affect the compound's electronic properties and steric hindrance, potentially impacting its interactions in biological systems. Overall, B-(2,5-Dichloro-3-fluorophenyl)boronic acid is a versatile compound with significant implications in both synthetic and pharmaceutical chemistry.

Formula: C₆H₄BCl₂FO₂

InChI: InChI=1S/C6H4BCl2FO2/c8-3-1-4(7(11)12)6(9)5(10)2-3/h1-2,11-12H

InChI key: InChIKey=VLKZUOKRWNZSPW-UHFFFAOYSA-N

SMILES: FC1=CC(Cl)=CC(B(O)O)=C1Cl

Synonyms:

• B-(2,5-Dichloro-3-fluorophenyl)boronic acid
• Boronic acid, B-(2,5-dichloro-3-fluorophenyl)-

(2,5-Dichloro-3-fluorophenyl)boronic acid

CAS: 2121511-41-7

• Formula: C₆H₄BCl₂FO₂
• Purity: 95%
• Color and Shape: Solid
• Molecular weight: 208.81016320000003

(2,5-Dichloro-3-fluorophenyl)boronic acid

CAS: 2121511-41-7

• Purity: 98%
• Molecular weight: 208.81g/mol

(2,5-Dichloro-3-fluorophenyl)boronic acid

CAS: 2121511-41-7

• Purity: 98%
• Molecular weight: 208.8000030517578

2,5-Dichloro-3-fluorophenylboronic acid

CAS: 2121511-41-7

Versatile small molecule scaffold

• Formula: C₆H₄BCl₂FO₂
• Purity: Min. 95%
• Molecular weight: 208.81 g/mol