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AE28196

1098340-27-2 | Methyl 4-(trifluoromethyl)-1h-indole-2-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $40.00 $28.00 -   +
1g 95% in stock $114.00 $80.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE28196
Chemical Name: Methyl 4-(trifluoromethyl)-1h-indole-2-carboxylate
CAS Number: 1098340-27-2
Molecular Formula: C11H8F3NO2
Molecular Weight: 243.1819
MDL Number: MFCD11655690
SMILES: COC(=O)c1cc2c([nH]1)cccc2C(F)(F)F

 

Computed Properties
Complexity: 306  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 3.3  

 

 

Upstream Synthesis Route
  • Methyl 4-(trifluoromethyl)-1H-indole-2-carboxylate is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its ability to participate in diverse chemical reactions.One of the key applications of Methyl 4-(trifluoromethyl)-1H-indole-2-carboxylate is in the synthesis of biologically active molecules. The trifluoromethyl group provides enhanced lipophilicity and metabolic stability to the resulting compounds, making them promising candidates for drug development. By incorporating this building block into a molecular structure, chemists can access a wide range of potential drug candidates with improved pharmacokinetic properties.Furthermore, Methyl 4-(trifluoromethyl)-1H-indole-2-carboxylate can be utilized in the preparation of advanced materials with tailored properties. Its fluorinated moiety can impart unique characteristics such as increased electron density, hydrophobicity, and thermal stability to the materials, making them suitable for applications in electronic devices, coatings, and catalysts.Overall, the use of Methyl 4-(trifluoromethyl)-1H-indole-2-carboxylate in chemical synthesis enables the efficient construction of complex molecules with enhanced functionalities, opening up possibilities for the development of new drugs, materials, and other important compounds in various scientific fields.
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