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Home  > Chemistry  > Organic Building Blocks  > Anhydrides  > 6-Iodo-2h-3,1-benzoxazine-2,4(1h)-dione

AA14641

116027-10-2 | 6-Iodo-2h-3,1-benzoxazine-2,4(1h)-dione

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.

Description
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

 

Computed Properties
Complexity: 256  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
XLogP3: 1.7  

 

 

Upstream Synthesis Route
  • 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.
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