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Home  > 5-Amino-3,4-dimethylisoxazole

AB08844

19947-75-2 | 5-Amino-3,4-dimethylisoxazole

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $35.00 $24.00 -   +
5g 98% in stock $116.00 $81.00 -   +
10g 98% in stock $220.00 $154.00 -   +
25g 98% in stock $459.00 $321.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB08844
Chemical Name: 5-Amino-3,4-dimethylisoxazole
CAS Number: 19947-75-2
Molecular Formula: C5H8N2O
Molecular Weight: 112.1298
MDL Number: MFCD00046081
SMILES: Cc1noc(c1C)N
NSC Number: 143787

 

Computed Properties
Complexity: 86.5  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 8  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
XLogP3: 0.8  

 

 

Upstream Synthesis Route
  • 3,4-Dimethylisoxazol-5-amine is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in organic synthesis, especially in the formation of heterocyclic compounds. Its isoxazole ring structure makes it an essential component in the preparation of pharmaceutically important molecules, agrochemicals, and advanced materials.In chemical synthesis, 3,4-Dimethylisoxazol-5-amine acts as a key intermediate in the creation of various biologically active compounds. Its presence in a reaction pathway can lead to the formation of diverse chemical structures, thereby expanding the scope of potential products that can be obtained. Additionally, the amine functional group present in this compound allows for further modification through reactions such as acylation, alkylation, or condensation, enabling the synthesis of more complex molecules.Furthermore, the unique electronic properties of 3,4-Dimethylisoxazol-5-amine make it a valuable tool in the design and synthesis of novel organic compounds with specific functionalities. Its ability to participate in both nucleophilic and electrophilic reactions broadens its utility in the development of structurally diverse compounds for various applications in medicinal chemistry, materials science, and other specialized fields.
Literature
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