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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)-

Cyclohexanecarboxylic acid, 4-(4-chlorophenyl)-, trans-

OC(=O)[C@@H]1CC[C@H](CC1)c1ccc(cc1)Cl Request for Quotation
Chemical Name: Cyclohexanecarboxylic acid, 4-(4-chlorophenyl)-, trans-
CAS Number: 49708-81-8
Product Number: AG00I8VQ(AGN-PC-0OB1LR)
Synonyms:
MDL No:
Molecular Formula: C13H15ClO2
Molecular Weight: 238.7100

Identification/Properties

Properties
MP:
252-254°C
BP:
387.1°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
238.711g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
238.076g/mol
Monoisotopic Mass:
238.076g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
238
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


Trans-4-(4-Chlorophenyl)cyclohexanecarboxylic acid plays a crucial role in chemical synthesis as a versatile building block for various organic compounds. Its unique structure allows for the modification of both the cyclohexane ring and the chlorophenyl group, enabling the creation of a diverse range of molecules with different properties and functions.In organic synthesis, trans-4-(4-Chlorophenyl)cyclohexanecarboxylic acid can be utilized as a starting material for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. By employing various chemical reactions such as esterification, amidation, and reduction, this compound can be transformed into derivatives with specific functionalities desired for particular applications.Moreover, trans-4-(4-Chlorophenyl)cyclohexanecarboxylic acid serves as a valuable intermediate in the preparation of complex organic molecules, including natural products and advanced materials. Its ability to undergo selective chemical transformations makes it a versatile tool for chemists seeking to design and synthesize novel compounds for various industrial and research purposes.