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AA53899

1217500-82-7 | 2-((Dimethylamino)methyl)-5-nitrophenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 96% in stock $401.00 $281.00 -   +
1g 96% in stock $1,178.00 $824.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA53899
Chemical Name: 2-((Dimethylamino)methyl)-5-nitrophenylboronic acid
CAS Number: 1217500-82-7
Molecular Formula: C9H13BN2O4
Molecular Weight: 224.0215
MDL Number: MFCD12025993
SMILES: CN(Cc1ccc(cc1B(O)O)[N+](=O)[O-])C

 

Computed Properties
Complexity: 244  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 3  

 

 

Upstream Synthesis Route
  • (2-((Dimethylamino)methyl)-5-nitrophenyl)boronic acid is commonly used in chemical synthesis as a versatile building block. Its unique properties make it a valuable reagent in various organic reactions, particularly in the field of medicinal and pharmaceutical chemistry.This compound is frequently employed in the Suzuki-Miyaura cross-coupling reaction, where it serves as a boronic acid source to facilitate the formation of carbon-carbon bonds. By reacting with suitable coupling partners under palladium catalysis, the boronic acid can be utilized to introduce the (dimethylamino)methyl and nitrophenyl groups into the desired molecules, enabling the synthesis of structurally diverse compounds.Additionally, (2-((Dimethylamino)methyl)-5-nitrophenyl)boronic acid can be utilized in the preparation of various functionalized materials, such as fluorescent dyes, ligands for catalysis, and molecular probes for biological studies. Its ability to react selectively with specific functional groups makes it a valuable tool for the design and construction of complex molecular architectures in organic synthesis.Overall, the application of (2-((Dimethylamino)methyl)-5-nitrophenyl)boronic acid in chemical synthesis offers chemists a powerful strategy to efficiently access novel compounds with diverse functionalities, making it an indispensable reagent in modern synthetic chemistry.
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