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AB39861

30418-59-8 | 3-Aminophenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $6.00 $4.00 -   +
5g 98% in stock $13.00 $9.00 -   +
100g 95% in stock $148.00 $104.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB39861
Chemical Name: 3-Aminophenylboronic acid
CAS Number: 30418-59-8
Molecular Formula: C6H8BNO2
Molecular Weight: 136.9442
MDL Number: MFCD00149554
SMILES: Nc1cccc(c1)B(O)O

 

Computed Properties
Complexity: 110  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • 3-Aminobenzeneboronic Acid, also known as 3-aminophenylboronic acid, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, it serves as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and materials.One of the primary applications of 3-Aminobenzeneboronic Acid is in the field of Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by palladium, involves the coupling of an aryl halide with an arylboronic acid to form a new carbon-carbon bond. 3-Aminobenzeneboronic Acid, with its boronic acid functional group, plays a crucial role as a partner in such cross-coupling reactions, enabling the synthesis of biaryl compounds, which are important in pharmaceutical development and materials science.Furthermore, 3-Aminobenzeneboronic Acid can be utilized in the preparation of fluorescent dyes and sensors. By incorporating this compound into the molecular structure of dyes, researchers can create fluorescent molecules with specific properties for biological imaging and detection applications. Its boronic acid moiety also makes it a valuable component in designing sensors for detecting sugars and other analytes based on the boronate affinity.Overall, 3-Aminobenzeneboronic Acid's presence in the toolbox of organic chemists highlights its significance in enabling the construction of complex molecular architectures and functional materials through various synthetic routes and applications.
Literature
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