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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1-(4-(Trifluoromethoxy)phenyl)cyclopropanecarboxylic acid

OC(=O)C1(CC1)c1ccc(cc1)OC(F)(F)F Request for Quotation
Chemical Name: 1-(4-(Trifluoromethoxy)phenyl)cyclopropanecarboxylic acid
CAS Number: 936727-93-4
Product Number: AG006ENV(AGN-PC-0WAJ1N)
Synonyms:
MDL No:
Molecular Formula: C11H9F3O3
Molecular Weight: 246.1826

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
246.185g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
3
Exact Mass:
246.05g/mol
Monoisotopic Mass:
246.05g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
302
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

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Chemical Structure


1-[4-(Trifluoromethoxy)phenyl]cyclopropanecarboxylic Acid is a versatile chemical reagent that finds wide application in organic synthesis. This compound is utilized as a building block in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Due to the presence of both a cyclopropane ring and a carboxylic acid functionality, this compound can undergo diverse chemical transformations leading to the formation of a variety of complex molecules. In organic synthesis, it is commonly employed as a key intermediate in the synthesis of biologically active compounds and drug candidates. Its unique structure imparts specific reactivity, making it a valuable tool for chemists to introduce structural diversity and complexity in their target molecules.