CAS 158937-25-8

(4'-(pentyloxy)(1,1'-biphenyl)-4-yl)boronic acid

Description:

(4'-(Pentyloxy)(1,1'-biphenyl)-4-yl)boronic acid, with the CAS number 158937-25-8, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a biphenyl structure. This compound features a pentyloxy substituent, which contributes to its hydrophobic properties and can influence its solubility in organic solvents. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and materials science. The biphenyl moiety provides stability and can enhance the electronic properties of the compound, making it suitable for use in organic electronics and as a building block in the synthesis of more complex molecules. Additionally, the presence of the pentyloxy group may affect the compound's physical properties, such as melting point and boiling point, as well as its reactivity in chemical reactions. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and materials development.

4'-Pentyloxybiphenyl-4-boronic Acid (contains varying amounts of Anhydride)

CAS: 158937-25-8

Formula: C₁₇H₂₁BO₃

Purity: 97.0 to 107.0 %

Color and Shape: White to Almost white powder to crystal

Molecular weight: 284.16

Ref: 3B-P2365

Boronic acid, B-[4'-(pentyloxy)[1,1'-biphenyl]-4-yl]-

CAS: 158937-25-8

Formula: C₁₇H₂₁BO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 284.1578

Ref: IN-DA001R15

[4'-(Pentyloxy)[1,1'-biphenyl]-4-yl]boronic acid

CAS: 158937-25-8

[4'-(Pentyloxy)[1,1'-biphenyl]-4-yl]boronic acid

Purity: 98%

Molecular weight: 284.16g/mol

Ref: 54-OR360568

(4′-(Pentyloxy)-[1,1′-biphenyl]-4-yl)boronic acid

CAS: 158937-25-8

Formula: C₁₇H₂₁BO₃

Purity: 98%

Molecular weight: 284.16

Ref: 10-F232309