CAS 115377-93-0

Boronic acid, [2-(methoxymethoxy)phenyl]-

Description:

Boronic acid, [2-(methoxymethoxy)phenyl]-, with the CAS number 115377-93-0, is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has a methoxymethoxy substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and materials science. The methoxymethoxy group enhances its solubility in organic solvents and may influence its reactivity and interaction with biological systems. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic chemistry. Additionally, this compound may exhibit unique properties based on its molecular structure, such as potential applications in drug development or as a building block in the synthesis of more complex molecules. Overall, its characteristics make it a valuable compound in both academic research and industrial applications.

Formula: C₈H₁₁BO₄

Boronic acid, B-[2-(methoxymethoxy)phenyl]-

CAS: 115377-93-0

Formula: C₈H₁₁BO₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 181.9815

Ref: IN-DA000GO1

2-(Methoxymethoxy)phenylboronic acid

CAS: 115377-93-0

2-(Methoxymethoxy)phenylboronic acid

Formula: C₈H₁₁BO₄

Purity: 98%

Color and Shape: white to off-white crystalline powder

Molecular weight: 181.98g/mol

Ref: 54-OR360202

(2-(Methoxymethoxy)phenyl)boronic acid

CAS: 115377-93-0

Formula: C₈H₁₁BO₄

Purity: 95%

Color and Shape: No data available.

Molecular weight: 181.98

Ref: 10-F338070