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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)-

Cyclopropanecarboxylic acid, 1-(4-chlorophenyl)-

OC(=O)C1(CC1)c1ccc(cc1)Cl Request for Quotation
Chemical Name: Cyclopropanecarboxylic acid, 1-(4-chlorophenyl)-
CAS Number: 72934-37-3
Product Number: AG0036P9(AGN-PC-0JM33S)
Synonyms:
MDL No: MFCD00001289
Molecular Formula: C10H9ClO2
Molecular Weight: 196.6303

Identification/Properties

Properties
MP:
152-155 °C
BP:
336.7°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Refractive Index:
1.5152 (estimate)
Computed Properties
Molecular Weight:
196.63g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
196.029g/mol
Monoisotopic Mass:
196.029g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
215
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-Chlorophenyl)cyclopropanecarboxylic acid is a versatile building block commonly used in chemical synthesis for the preparation of various organic compounds. Its compact cyclopropane ring structure imparts unique reactivity, making it a valuable tool in the creation of novel molecules. This compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and functional materials. Its ability to undergo diverse transformation reactions, such as nucleophilic substitution and cross-coupling reactions, allows for the efficient construction of complex molecular architectures. Furthermore, the presence of the 4-chlorophenyl group provides a handle for further functionalization, enabling the design of molecules with specific target properties. In the realm of organic synthesis, 1-(4-Chlorophenyl)cyclopropanecarboxylic acid plays a crucial role in enabling the rapid and controlled assembly of structurally diverse compounds with potential applications across various scientific disciplines.