CAS 117098-94-9

2,1-Benzoxaborol-6-amine, 1,3-dihydro-1-hydroxy-

Description:

2,1-Benzoxaborol-6-amine, 1,3-dihydro-1-hydroxy- is a chemical compound characterized by its unique structural features, which include a benzoxaborole core and an amine functional group. This compound typically exhibits properties associated with both boron and nitrogen functionalities, making it of interest in various chemical applications, particularly in medicinal chemistry. The presence of the hydroxyl group contributes to its potential reactivity and solubility in polar solvents. Benzoxaboroles are known for their ability to interact with biological targets, which can lead to significant pharmacological effects. The compound's molecular structure allows for potential hydrogen bonding and coordination with other molecules, enhancing its utility in drug design and development. Additionally, the compound may exhibit specific stereochemical properties that influence its biological activity. Overall, 2,1-Benzoxaborol-6-amine, 1,3-dihydro-1-hydroxy- represents a class of compounds that bridge organic chemistry and medicinal applications, warranting further investigation into its properties and potential uses.

Formula: C₇H₈BNO₂

5-Amino-2-(hydroxymethyl)phenylboronic Acid Cyclic Monoester

CAS: 117098-94-9

Formula: C₇H₈BNO₂

Purity: >95.0%(T)(HPLC)

Color and Shape: Light orange to Yellow to Green powder to crystal

Molecular weight: 148.96

Ref: 3B-A2559

6-Amino-3H-2,1-benzoxaborol-1-ol

CAS: 117098-94-9

Formula: C₇H₈BNO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 148.9549

Ref: IN-DA000DPZ

6-Amino-3H-2,1-benzoxaborol-1-ol

CAS: 117098-94-9

6-Amino-3H-2,1-benzoxaborol-1-ol

Purity: 98%

Color and Shape: Solid

Molecular weight: 148.95g/mol

Ref: 54-OR360633

6-Aminobenzo[c][1,2]oxaborol-1(3H)-ol

CAS: 117098-94-9

Formula: C₇H₈BNO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 148.96

Ref: 10-F231251

5-Aminoboronphthalide

Controlled Product

CAS: 117098-94-9

Applications 5-Aminoboronphthalide is used as a reactant in the preparation of 2,1-benzoxaborole peptide isoquinoline derivatives as HCV NS3 protease inhibitors. It is also used as reactant in the synthesis of nanocarrier for chemomechanically driven guest delivery fueled by intracellular ATP.
References Li, X., et al.: Bioorg. Med. Chem. Lett., 21, 2048 (2011); Biswas, S., et al.: Nat. Chem., 5, 613 (2013);

Formula: C₇H₈BNO₂

Color and Shape: Neat

Molecular weight: 148.955

Ref: TR-A622575

5-Amino-2-(hydroxymethyl)phenylboronic Acid Cyclic Monoester

CAS: 117098-94-9

5-Amino-2-(hydroxymethyl)phenylboronic acid cyclic monoester is an organic compound that is a ligand for metal ions. It binds to metal ions by donating a hydrogen atom from the hydroxyl group and forming a covalent bond with the metal ion. This ligand has been used in the synthesis of nanoparticles and it has also been used as a ligand in binding constants and affinity constants. 5-Amino-2-(hydroxymethyl)phenylboronic acid cyclic monoester has been shown to have high affinity for phenylboronic acid. This ligand undergoes nucleophilic attack by water, which leads to the release of boric acid and alcohol.

Formula: C₇H₈BNO₂

Purity: Min. 95%

Molecular weight: 148.96 g/mol

Ref: 3D-SEA09894