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AE24551

1057107-39-7 | 4-(2-(Methoxycarbonyl)cyclopropyl)benzoic acid

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 $758.00 $531.00 -   +
10g 98% in stock $1,317.00 $922.00 -   +
25g 98% in stock $2,623.00 $1,836.00 -   +

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*All prices are in USD.

Description
Catalog Number: AE24551
Chemical Name: 4-(2-(Methoxycarbonyl)cyclopropyl)benzoic acid
CAS Number: 1057107-39-7
Molecular Formula: C12H12O4
Molecular Weight: 220.2213
MDL Number: MFCD22393665
SMILES: COC(=O)C1CC1c1ccc(cc1)C(=O)O

 

Computed Properties
Complexity: 291  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 4  
Undefined Atom Stereocenter Count: 2  
XLogP3: 1.5  

 

 

Upstream Synthesis Route
  • 4-(2-(Methoxycarbonyl)cyclopropyl)benzoic acid, a versatile compound with an intricate chemical structure, serves as a key building block in organic synthesis. This compound features a cyclopropyl group functionalized with a methoxycarbonyl moiety, offering a unique reactivity profile that can be leveraged in various synthetic pathways. In chemical synthesis, 4-(2-(Methoxycarbonyl)cyclopropyl)benzoic acid finds application as a valuable intermediate for the construction of complex molecules with pharmaceutical, agrochemical, and materials science relevance. The cyclopropyl motif imparts rigidity and sterics to the molecule, influencing the overall three-dimensional shape and properties of the compounds derived from it. Furthermore, the presence of the benzoic acid moiety allows for further derivatization through traditional organic transformations such as esterifications, amidations, and nucleophilic substitutions. This versatility enables the synthesis of a diverse array of analogs and derivatives that can be explored for their biological activities or material properties.Overall, the strategic incorporation of 4-(2-(Methoxycarbonyl)cyclopropyl)benzoic acid in organic synthesis provides chemists with a powerful tool to access structurally complex and diverse chemical space, facilitating the discovery and development of novel compounds with potential applications across various scientific disciplines.
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