AA14641
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 95% | in stock | $43.00 | $30.00 | - + | |
250mg | 95% | in stock | $52.00 | $37.00 | - + | |
1g | 95% | in stock | $102.00 | $72.00 | - + | |
5g | 95% | in stock | $125.00 | $88.00 | - + | |
10g | 95% | in stock | $250.00 | $175.00 | - + | |
25g | 95% | in stock | $612.00 | $429.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA14641 |
Chemical Name: | 6-Iodo-2h-3,1-benzoxazine-2,4(1h)-dione |
CAS Number: | 116027-10-2 |
Molecular Formula: | C8H4INO3 |
Molecular Weight: | 289.0267 |
MDL Number: | MFCD06661932 |
SMILES: | Ic1ccc2c(c1)c(=O)oc(=O)[nH]2 |
NSC Number: | 163036 |
Complexity: | 256 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
XLogP3: | 1.7 |
6-Iodo-2H-3,1-benzoxazin-2,4(1H)-dione is a versatile compound widely used in chemical synthesis as a valuable building block. Due to its unique structure and reactivity, this compound serves as an important intermediate in the synthesis of various organic compounds.One of the key applications of 6-Iodo-2H-3,1-benzoxazin-2,4(1H)-dione is its use in the preparation of heterocyclic compounds. Its iodo-substituted benzoxazinone scaffold enables the introduction of diverse functional groups through various synthetic transformations. This compound can undergo substitution, addition, or elimination reactions to yield new derivatives with modified properties.Additionally, 6-Iodo-2H-3,1-benzoxazin-2,4(1H)-dione is employed in the synthesis of biologically active molecules, pharmaceuticals, and agrochemicals. By strategically modifying the structure of this compound, chemists can design and synthesize new compounds with enhanced activities or properties for a range of applications.Furthermore, the presence of the iodo group in 6-Iodo-2H-3,1-benzoxazin-2,4(1H)-dione allows for further functionalization through cross-coupling reactions, providing access to more complex molecules. This versatility makes it a valuable tool in the arsenal of synthetic chemists for creating novel compounds with potential applications in various fields.