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AD45503

1041205-25-7 | Methyl 3-iodo-1-methyl-1H-indazole-6-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $105.00 $74.00 -   +
1g 98% in stock $249.00 $175.00 -   +
5g 98% in stock $712.00 $498.00 -   +
10g 98% in stock $1,179.00 $825.00 -   +
25g 98% in stock $2,111.00 $1,478.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AD45503
Chemical Name: Methyl 3-iodo-1-methyl-1H-indazole-6-carboxylate
CAS Number: 1041205-25-7
Molecular Formula: C10H9IN2O2
Molecular Weight: 316.0951
MDL Number: MFCD15071434
SMILES: COC(=O)c1ccc2c(c1)n(C)nc2I

 

Computed Properties
Complexity: 262  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 2  
XLogP3: 2.1  

 

 

Upstream Synthesis Route
  • The Methyl 3-iodo-1-methyl-1H-indazole-6-carboxylate is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its structural composition allows for efficient incorporation into complex molecular structures, making it an essential component in the development of novel compounds.In chemical synthesis, Methyl 3-iodo-1-methyl-1H-indazole-6-carboxylate can be employed as a key intermediate in the preparation of indazole derivatives. Through various synthetic routes and reactions, this compound can be transformed into a diverse range of functionalized molecules with potential applications in drug discovery and material science. Its ability to undergo selective transformations makes it a valuable tool for accessing structurally diverse compounds with enhanced biological or physical properties.Furthermore, the presence of the iodo and ester functional groups in this compound enables further functionalization through cross-coupling reactions, nucleophilic substitutions, and other transformations. By judiciously modifying these functional groups, chemists can tailor the properties of the resulting molecules to suit specific application requirements. Overall, the Methyl 3-iodo-1-methyl-1H-indazole-6-carboxylate plays a crucial role in expanding the synthetic toolbox for the creation of innovative chemical entities with potential industrial and therapeutic relevance.
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