4-(N-BOC-amino)benzeneboronic acid

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Category:Pharmaceutical Materials   Own Brand:MT  /MOQ:100KG  /From China/  B2B only.

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Introduction

CAS.No:380430-49-9

Appearance:White powder

Molecular Formula:C11H16BNO4

Purity:HPLC≥99.5%

Molecular weight:237.06

Application:20 tons/month

 

Property Details
Molecular Formula C11H16BNO4
Molecular Weight 237.06 g/mol
Appearance White to off-white crystalline solid or powder
Purity Typically ≥95%
Melting Point 220-225 °C (decomposition may occur)
Boiling Point Predicted to be above 300 °C at 760 mmHg
Density Approximately 1.2 g/cm³ (Predicted)
Solubility Soluble in organic solvents such as DMSO, DMF, and methanol; slightly soluble in water
Applications Organic synthesis, Suzuki-Miyaura coupling reactions, drug discovery, and biochemical research
Safety Considerations Handle with care; avoid contact with skin and eyes; store in a cool, dry place away from moisture and strong acids
Suppliers Available from specialized chemical suppliers

Applications

4-(N-BOC-Amino)benzeneboronic acid is a versatile compound widely used in organic synthesis, particularly in Suzuki-Miyaura coupling reactions. Its boronic acid group and protected amine functionality provide unique reactivity, allowing for the formation of carbon-carbon bonds with various aryl and vinyl halides while maintaining the potential for further amine functionalization.

In drug discovery, this compound serves as a key intermediate in the synthesis of novel pharmaceutical compounds. The tert-butoxycarbonyl (BOC) protecting group can be easily removed under mild conditions, enabling the introduction of diverse amine functionalities. This flexibility makes 4-(N-BOC-Amino)benzeneboronic acid a valuable tool in the development of new therapeutic agents.

Its solubility in organic solvents facilitates its use in various synthetic methodologies, while its stability under appropriate storage conditions ensures its reliability in research and industrial applications. Additionally, this compound finds applications in biochemical research, where it is used to explore new chemical entities and biological pathways.

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