AE16783
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 97% | in stock | $32.00 | $22.00 | - + | |
250mg | 97% | in stock | $50.00 | $35.00 | - + | |
1g | 97% | in stock | $99.00 | $69.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE16783 |
Chemical Name: | Methyl 2,3-dioxoindoline-7-carboxylate |
CAS Number: | 103030-10-0 |
Molecular Formula: | C10H7NO4 |
Molecular Weight: | 205.1669 |
MDL Number: | MFCD00612499 |
SMILES: | COC(=O)c1cccc2c1NC(=O)C2=O |
Complexity: | 325 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 15 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 2 |
XLogP3: | 0.6 |
Methyl 2,3-dioxoindoline-7-carboxylate is a versatile compound that finds widespread application in chemical synthesis. It serves as a key building block in the production of various organic molecules with pharmaceutical, agricultural, and material science importance.In chemical synthesis, Methyl 2,3-dioxoindoline-7-carboxylate acts as a valuable precursor for the preparation of indole derivatives. Its reactivity at the C-3 position allows for the introduction of different functional groups, enabling the synthesis of a diverse array of indoline-based compounds. These derivatives have demonstrated biological activities, making them important targets for drug discovery and development.Furthermore, Methyl 2,3-dioxoindoline-7-carboxylate can participate in various reactions such as condensation, cycloaddition, and substitution processes. This broad reactivity profile enhances its utility in constructing complex molecules with specific structural motifs. Additionally, its stability under common reaction conditions makes it a reliable component in multi-step synthesis strategies.Overall, Methyl 2,3-dioxoindoline-7-carboxylate is a valuable tool for chemists engaged in the design and preparation of novel organic compounds. Its versatility and ease of manipulation make it a preferred choice for achieving diverse molecular architectures with potential applications in various scientific fields.