Cas no 56042-77-4 (2-(Dimethylamino)benzamide)

2-(Dimethylamino)benzamide is a versatile organic compound characterized by its dimethylamino and benzamide functional groups. This structure imparts unique reactivity, making it valuable as an intermediate in pharmaceutical and agrochemical synthesis. Its electron-donating dimethylamino group enhances its utility in coupling reactions and as a precursor for heterocyclic compounds. The compound exhibits good solubility in common organic solvents, facilitating its use in diverse reaction conditions. Its stability under standard storage conditions ensures reliable handling in industrial and research settings. Applications include its role in developing bioactive molecules, where its modular structure allows for further functionalization. Proper handling requires adherence to standard safety protocols for amine-containing compounds.
2-(Dimethylamino)benzamide structure
2-(Dimethylamino)benzamide structure
Product Name:2-(Dimethylamino)benzamide
CAS No:56042-77-4
MF:C9H12N2O
MW:164.204381942749
CID:1038198
PubChem ID:22478068
Update Time:2025-10-19

2-(Dimethylamino)benzamide Chemical and Physical Properties

Names and Identifiers

    • 2-(Dimethylamino)benzamide
    • 2-dimethylamino-benzamide
    • (dimethylamino)benzamide
    • DTXSID30625982
    • Benzamide, 2-(dimethylamino)-
    • 56042-77-4
    • A870036
    • KTAOWCOLDQWGHV-UHFFFAOYSA-N
    • SCHEMBL147847
    • MDL: MFCD15833009
    • Inchi: 1S/C9H12N2O/c1-11(2)8-6-4-3-5-7(8)9(10)12/h3-6H,1-2H3,(H2,10,12)
    • InChI Key: KTAOWCOLDQWGHV-UHFFFAOYSA-N
    • SMILES: O=C(C1C=CC=CC=1N(C)C)N

Computed Properties

  • Exact Mass: 164.094963011g/mol
  • Monoisotopic Mass: 164.094963011g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 168
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.4
  • Topological Polar Surface Area: 46.3?2

2-(Dimethylamino)benzamide Pricemore >>

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Additional information on 2-(Dimethylamino)benzamide

Introduction to 2-(Dimethylamino)benzamide (CAS No. 56042-77-4)

2-(Dimethylamino)benzamide (CAS No. 56042-77-4) is a versatile organic compound with significant applications in various fields, including pharmaceuticals, agrochemicals, and materials science. This compound is characterized by its unique chemical structure, which combines a benzamide group with a dimethylamino substituent. The benzamide moiety provides aromatic stability and reactivity, while the dimethylamino group introduces basicity and enhances solubility in polar solvents.

The synthesis of 2-(Dimethylamino)benzamide involves several methods, including the reaction of dimethylamine with benzoyl chloride in the presence of a suitable catalyst. Recent advancements in catalytic systems have enabled more efficient and environmentally friendly syntheses, reducing production costs and minimizing waste. Researchers have also explored the use of microwave-assisted synthesis to accelerate reaction times and improve yields.

One of the most promising applications of 2-(Dimethylamino)benzamide is in the field of drug discovery. Its structure makes it an ideal candidate for modifying bioactive molecules, enhancing their pharmacokinetic properties. For instance, studies have shown that this compound can act as a precursor for developing inhibitors of certain enzymes, such as histone deacetylases (HDACs), which are targets for cancer therapy.

In agrochemicals, 2-(Dimethylamino)benzamide has been investigated as a potential herbicide or fungicide. Its ability to interact with biological membranes and disrupt cellular processes makes it a valuable lead compound for developing safer and more effective agricultural chemicals. Recent research has focused on optimizing its stability under environmental conditions to ensure long-lasting efficacy.

The environmental impact of 2-(Dimethylamino)benzamide has also been a topic of interest. Studies have shown that it degrades relatively quickly under aerobic conditions, reducing its persistence in soil and water systems. However, further research is needed to fully understand its ecological effects and ensure sustainable use.

From a materials science perspective, 2-(Dimethylamino)benzamide has been explored as a component in advanced materials such as polymers and coatings. Its ability to form hydrogen bonds and participate in supramolecular interactions makes it a valuable building block for designing functional materials with tailored properties.

In conclusion, 2-(Dimethylamino)benzamide (CAS No. 56042-77-4) is a multifaceted compound with wide-ranging applications across various industries. Ongoing research continues to uncover new potential uses and optimize its properties, ensuring its relevance in the ever-evolving landscape of chemical innovation.

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