Cyclopropanecarboxylic acid, 1-(trifluoromethyl)-, ethyl ester


Chemical Name: Cyclopropanecarboxylic acid, 1-(trifluoromethyl)-, ethyl ester
CAS Number: 139229-57-5
Product Number: AG001AJP(AGN-PC-0039UI)
Synonyms:
MDL No:
Molecular Formula: C7H9F3O2
Molecular Weight: 182.1404

Identification/Properties


Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
182.142g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
182.055g/mol
Monoisotopic Mass:
182.055g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
193
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



Ethyl 1-(trifluoromethyl)cyclopropanecarboxylate, commonly known as $name$, is a versatile compound frequently utilized in chemical synthesis. Its unique structure, featuring a trifluoromethyl group attached to a cyclopropane ring, imparts distinctive properties that make it a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, $name$ serves as a key reagent for introducing the trifluoromethyl moiety into organic molecules, a modification that can significantly enhance the biological activity or physical properties of the resulting compounds. The presence of the trifluoromethyl group in $name$ confers enhanced lipophilicity, metabolic stability, and binding affinity, making it particularly useful in drug discovery and development.Moreover, the cyclopropane ring in $name$ offers exciting synthetic opportunities due to its strained nature, which can lead to highly regioselective and stereoselective reactions. By utilizing the unique structural features of $name$, chemists can access novel chemical scaffolds and molecular architectures that may not be readily achievable with traditional building blocks.From the synthesis of complex natural products to the development of new materials with tailored properties, the application of Ethyl 1-(trifluoromethyl)cyclopropanecarboxylate in chemical synthesis continues to expand the frontiers of organic chemistry and drive innovation in diverse fields.