Cas no 98960-81-7 (2-amino-N-(2-aminoethyl)benzamide)

2-Amino-N-(2-aminoethyl)benzamide is a bifunctional organic compound featuring both primary amine and amide functional groups. Its molecular structure, comprising a benzamide core with an ethylenediamine side chain, makes it a versatile intermediate in organic synthesis and pharmaceutical applications. The compound’s dual amine functionality allows for selective derivatization, enabling its use in the preparation of heterocycles, peptidomimetics, and chelating agents. Its stability under mild conditions and compatibility with standard coupling reagents enhance its utility in medicinal chemistry and materials science. The product is typically characterized by high purity (>95%) and is supplied as a solid, ensuring consistent performance in research and industrial processes.
2-amino-N-(2-aminoethyl)benzamide structure
98960-81-7 structure
Product Name:2-amino-N-(2-aminoethyl)benzamide
CAS No:98960-81-7
MF:C9H13N3O
MW:179.219021558762
CID:1991694
PubChem ID:39733689
Update Time:2025-06-07

2-amino-N-(2-aminoethyl)benzamide Chemical and Physical Properties

Names and Identifiers

    • Benzamide, 2-amino-N-(2-aminoethyl)-
    • 2-Amino-N-(2-aminoethyl)benzamide
    • AKOS010498951
    • 98960-81-7
    • MFCD11869114
    • SCHEMBL890994
    • CS-0237806
    • F72249
    • EN300-187189
    • 2-amino-N-(2-aminoethyl)benzamide
    • Inchi: 1S/C9H13N3O/c10-5-6-12-9(13)7-3-1-2-4-8(7)11/h1-4H,5-6,10-11H2,(H,12,13)
    • InChI Key: CPVBIJDFUDYJIO-UHFFFAOYSA-N
    • SMILES: O=C(C1C=CC=CC=1N)NCCN

Computed Properties

  • Exact Mass: 179.106
  • Monoisotopic Mass: 179.106
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 3
  • Complexity: 172
  • 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: 81.1A^2

Experimental Properties

  • Density: 1.177
  • Boiling Point: 412.3 °C at 760 mmHg
  • Flash Point: 203.1 °C

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2-amino-N-(2-aminoethyl)benzamide Suppliers

Amadis Chemical Company Limited
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Audited Supplier Audited Supplier
(CAS:98960-81-7)2-amino-N-(2-aminoethyl)benzamide
Order Number:A1221875
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 18:35
Price ($):272

2-amino-N-(2-aminoethyl)benzamide Related Literature

Additional information on 2-amino-N-(2-aminoethyl)benzamide

Comprehensive Overview of Benzamide, 2-amino-N-(2-aminoethyl)- (CAS No. 98960-81-7): Properties, Applications, and Market Insights

Benzamide, 2-amino-N-(2-aminoethyl)- (CAS No. 98960-81-7) is a specialized organic compound that has garnered significant attention in the fields of pharmaceutical research, material science, and biochemical applications. This compound, characterized by its unique aminoethyl and benzamide functional groups, plays a pivotal role in the synthesis of advanced materials and bioactive molecules. Its molecular structure, C9H13N3O, offers a versatile platform for chemical modifications, making it a valuable intermediate in various industrial and research settings.

The growing interest in 2-amino-N-(2-aminoethyl)benzamide is driven by its potential applications in drug discovery and development. Researchers are particularly intrigued by its ability to act as a building block for peptide mimetics and small molecule inhibitors, which are crucial in targeting specific biological pathways. Recent studies have explored its utility in designing enzyme inhibitors and receptor modulators, aligning with the current trend of personalized medicine and targeted therapies. This compound's compatibility with green chemistry principles further enhances its appeal in sustainable pharmaceutical manufacturing.

In the realm of material science, Benzamide, 2-amino-N-(2-aminoethyl)- serves as a precursor for polymeric materials and coating agents. Its bifunctional nature allows for cross-linking reactions, contributing to the development of high-performance polymers with enhanced thermal and mechanical properties. Industries are increasingly adopting this compound to produce advanced adhesives and protective coatings, addressing the demand for durable and eco-friendly materials. The compound's role in nanotechnology applications, such as surface functionalization of nanoparticles, is also under active investigation.

The market dynamics for CAS No. 98960-81-7 reflect its expanding applications. With the rise of biopharmaceuticals and smart materials, the demand for high-purity 2-amino-N-(2-aminoethyl)benzamide is expected to grow steadily. Suppliers are focusing on scalable synthesis methods to meet the needs of research institutions and industrial players. Additionally, regulatory compliance and quality control remain critical factors, as the compound's purity directly impacts its performance in end-use applications.

From a technical perspective, the synthesis of Benzamide, 2-amino-N-(2-aminoethyl)- involves multi-step organic reactions, often starting from 2-aminobenzoic acid or its derivatives. Optimizing reaction conditions to achieve high yields and minimal by-products is a key area of research. Analytical techniques such as HPLC and mass spectrometry are employed to ensure the compound's purity and structural integrity. These advancements align with the broader industry shift toward process intensification and quality-by-design principles.

Environmental and safety considerations are paramount when handling 98960-81-7. While the compound is not classified as hazardous under standard regulations, proper storage conditions—such as protection from moisture and extreme temperatures—are recommended to maintain its stability. Researchers and manufacturers are encouraged to follow good laboratory practices (GLP) and occupational safety guidelines to ensure safe usage.

Looking ahead, the future of Benzamide, 2-amino-N-(2-aminoethyl)- appears promising, with ongoing research exploring its potential in bioimaging and drug delivery systems. Collaborative efforts between academia and industry are likely to uncover new applications, further solidifying its position as a versatile chemical entity. As the scientific community continues to innovate, this compound is poised to play a critical role in addressing contemporary challenges in healthcare and advanced materials.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:98960-81-7)2-amino-N-(2-aminoethyl)benzamide
A1221875
Purity:99%
Quantity:1g
Price ($):272
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