Cas no 89530-95-0 (2,3-Dimethyl-3-butenamide)

2,3-Dimethyl-3-butenamide structure
2,3-Dimethyl-3-butenamide structure
Product Name:2,3-Dimethyl-3-butenamide
CAS No:89530-95-0
MF:C6H11NO
MW:113.157641649246
CID:4735555
Update Time:2025-04-23

2,3-Dimethyl-3-butenamide Chemical and Physical Properties

Names and Identifiers

    • 2,3-dimethyl-but-3-enoic acid amide
    • 2,3-Dimethyl-3-butenamide
    • Inchi: 1S/C6H11NO/c1-4(2)5(3)6(7)8/h5H,1H2,2-3H3,(H2,7,8)
    • InChI Key: LWBALMKJFWPQBS-UHFFFAOYSA-N
    • SMILES: O=C(C(C)C(=C)C)N

Computed Properties

  • Exact Mass: 113.084
  • Monoisotopic Mass: 113.084
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 2
  • Complexity: 118
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 43.1

2,3-Dimethyl-3-butenamide Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
D365990-25mg
2,3-Dimethyl-3-butenamide
89530-95-0
25mg
$310.00 2023-05-18
TRC
D365990-100mg
2,3-Dimethyl-3-butenamide
89530-95-0
100mg
$1143.00 2023-05-18
TRC
D365990-250mg
2,3-Dimethyl-3-butenamide
89530-95-0
250mg
$2566.00 2023-05-18

Additional information on 2,3-Dimethyl-3-butenamide

2,3-Dimethyl-but-3-enoic acid amide (CAS No: 89530-95-0)

2,3-Dimethyl-but-3-enoic acid amide, also known by its CAS number 89530-95-0, is a versatile organic compound with significant applications in various industries. This compound is a derivative of 2,3-dimethyl-but-3-enoic acid, where the carboxylic acid group is replaced by an amide functional group. The structure of this compound consists of a four-carbon chain with two methyl groups attached to the second and third carbons, and a double bond between the third and fourth carbons. The presence of the amide group imparts unique chemical properties, making it suitable for a wide range of applications.

Recent studies have highlighted the importance of 2,3-dimethyl-but-3-enoic acid amide in the field of biochemistry and pharmaceuticals. Researchers have explored its potential as a precursor for synthesizing bioactive molecules, including antioxidants and anti-inflammatory agents. The compound's ability to undergo various chemical transformations, such as amide bond formation and alkylation, has made it a valuable intermediate in organic synthesis.

In the context of agricultural chemistry, 2,3-dimethyl-but-3-enoic acid amide has been investigated for its role in plant growth regulation. Studies suggest that it may act as a signaling molecule in plants, influencing processes such as flowering time and stress responses. This finding opens new avenues for its application in developing eco-friendly pesticides and growth enhancers.

The synthesis of 2,3-dimethyl-but-3-enoic acid amide typically involves the reaction of 2,3-dimethyl-but-3-enoic acid with an appropriate amine in the presence of a coupling agent. Recent advancements in catalytic methods have improved the efficiency and selectivity of this reaction, reducing production costs and environmental impact. These developments are particularly relevant for industries relying on large-scale production of this compound.

From an environmental perspective, understanding the degradation pathways of 2,3-dimethyl-but-3-enamide is crucial for assessing its ecological impact. Research indicates that it undergoes rapid biodegradation under aerobic conditions, minimizing its persistence in natural ecosystems. This property is advantageous for its use in agricultural and industrial settings where environmental safety is a priority.

In conclusion, 2,3-dimethyl-but-3-enamide (CAS No: 89530-95) is a multifaceted compound with promising applications across diverse fields. Its chemical versatility, coupled with recent research advancements, positions it as a key player in modern organic synthesis and sustainable chemistry practices.

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