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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)-

2-(2-methoxyphenyl)cyclopropane-1-carboxylic acid

COc1ccccc1C1CC1C(=O)O Request for Quotation
Chemical Name: 2-(2-methoxyphenyl)cyclopropane-1-carboxylic acid
CAS Number: 92016-93-8
Product Number: AG00IGZT(AGN-PC-00OIZB)
Synonyms:
MDL No:
Molecular Formula: C11H12O3
Molecular Weight: 192.2112

Identification/Properties

Computed Properties
Molecular Weight:
192.214g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
192.079g/mol
Monoisotopic Mass:
192.079g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
227
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(2-Methoxyphenyl)cyclopropanecarboxylic acid is a versatile compound commonly used in chemical synthesis for its unique structural properties and reactivity. This compound serves as a key building block in organic chemistry, particularly in the synthesis of various pharmaceuticals, agrochemicals, and functional materials.Its cyclopropane ring imparts rigidity and sterically demanding characteristics, making it a valuable tool in designing bioactive molecules with enhanced selectivity and potency. The presence of the methoxyphenyl group provides a handle for further derivatization, allowing chemists to tailor the compound's properties for specific applications.In chemical synthesis, 2-(2-Methoxyphenyl)cyclopropanecarboxylic acid can participate in a range of reactions such as Grignard reactions, cross-coupling reactions, and ring-opening reactions to introduce new functionalities or construct complex molecular frameworks. Its ability to undergo diverse transformations makes it a valuable intermediate in the preparation of structurally intricate and biologically active compounds.Overall, the strategic incorporation of 2-(2-Methoxyphenyl)cyclopropanecarboxylic acid in chemical synthesis enables efficient access to diverse chemical space and facilitates the discovery of novel molecules with potential therapeutic or industrial applications.