Cas no 743441-87-4 (N-2-(Butan-2-yl)phenyl-2-chloropropanamide)

N-2-(Butan-2-yl)phenyl-2-chloropropanamide structure
743441-87-4 structure
Product Name:N-2-(Butan-2-yl)phenyl-2-chloropropanamide
CAS No:743441-87-4
MF:C13H18ClNO
MW:239.741122722626
CID:3106670
PubChem ID:3299302
Update Time:2025-07-22

N-2-(Butan-2-yl)phenyl-2-chloropropanamide Chemical and Physical Properties

Names and Identifiers

    • N-(2-sec-Butylphenyl)-2-chloropropanamide
    • SR-01000050408
    • Z56968527
    • FB169932
    • SR-01000050408-1
    • 743441-87-4
    • EN300-08450
    • N-[2-(butan-2-yl)phenyl]-2-chloropropanamide
    • AKOS000122389
    • 2-CHLORO-N-[2-(SEC-BUTYL)PHENYL]PROPANAMIDE
    • AKOS016881290
    • N-(2-butan-2-ylphenyl)-2-chloropropanamide
    • N-2-(Butan-2-yl)phenyl-2-chloropropanamide
    • Inchi: 1S/C13H18ClNO/c1-4-9(2)11-7-5-6-8-12(11)15-13(16)10(3)14/h5-10H,4H2,1-3H3,(H,15,16)
    • InChI Key: NLKTVLRJPSPMJX-UHFFFAOYSA-N
    • SMILES: ClC(C)C(NC1C=CC=CC=1C(C)CC)=O

Computed Properties

  • Exact Mass: 239.1076919Da
  • Monoisotopic Mass: 239.1076919Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 4
  • Complexity: 232
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 2
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 3.3
  • Topological Polar Surface Area: 29.1?2

N-2-(Butan-2-yl)phenyl-2-chloropropanamide Pricemore >>

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Additional information on N-2-(Butan-2-yl)phenyl-2-chloropropanamide

Comprehensive Overview of N-2-(Butan-2-yl)phenyl-2-chloropropanamide (CAS No. 743441-87-4)

N-2-(Butan-2-yl)phenyl-2-chloropropanamide, identified by its CAS number 743441-87-4, is a specialized organic compound with significant applications in pharmaceutical and agrochemical research. This compound belongs to the class of chloropropanamide derivatives, which are widely studied for their potential in drug development and crop protection. The unique structural features of this molecule, including the butan-2-ylphenyl moiety and the 2-chloropropanamide group, contribute to its distinct chemical properties and reactivity.

In recent years, the demand for N-2-(Butan-2-yl)phenyl-2-chloropropanamide has surged due to its role in the synthesis of novel bioactive molecules. Researchers are particularly interested in its potential as a building block for drug discovery, especially in the development of targeted therapies for various health conditions. The compound's CAS number 743441-87-4 is frequently searched in scientific databases, reflecting its growing importance in the field of medicinal chemistry.

One of the key advantages of N-2-(Butan-2-yl)phenyl-2-chloropropanamide is its versatility in chemical reactions. The presence of the chloropropanamide group allows for facile modifications, making it a valuable intermediate in the synthesis of more complex molecules. This characteristic has led to its widespread use in high-throughput screening and combinatorial chemistry, where rapid access to diverse chemical libraries is essential.

The compound's butan-2-ylphenyl moiety also plays a critical role in its biological activity. This structural feature enhances the molecule's lipophilicity, improving its ability to cross cell membranes and interact with intracellular targets. As a result, N-2-(Butan-2-yl)phenyl-2-chloropropanamide has been explored as a potential candidate for the development of enzyme inhibitors and receptor modulators.

In the agrochemical sector, N-2-(Butan-2-yl)phenyl-2-chloropropanamide has garnered attention for its potential use in crop protection. Researchers are investigating its efficacy as a precursor for herbicides and fungicides, leveraging its unique chemical properties to develop more sustainable and effective solutions for modern agriculture. The compound's CAS number 743441-87-4 is often referenced in patents and research papers related to agrochemical innovation.

From a synthetic perspective, the preparation of N-2-(Butan-2-yl)phenyl-2-chloropropanamide involves a series of well-established organic reactions. The key steps typically include the acylation of aniline derivatives followed by chlorination to introduce the 2-chloropropanamide group. These processes are optimized to ensure high yield and purity, meeting the stringent requirements of pharmaceutical and agrochemical applications.

The growing interest in N-2-(Butan-2-yl)phenyl-2-chloropropanamide is also reflected in the increasing number of scientific publications and patents citing its CAS number 743441-87-4. Researchers are continuously exploring new synthetic routes and applications for this compound, driven by the need for innovative solutions in drug discovery and crop protection. Its potential to address current challenges in these fields makes it a subject of ongoing investigation.

In conclusion, N-2-(Butan-2-yl)phenyl-2-chloropropanamide (CAS No. 743441-87-4) is a versatile and valuable compound with broad applications in pharmaceutical and agrochemical research. Its unique structural features, including the butan-2-ylphenyl and 2-chloropropanamide groups, contribute to its distinct chemical and biological properties. As research progresses, this compound is expected to play an increasingly important role in the development of novel therapeutics and agricultural solutions.

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