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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)-

Benzoic acid, 4-(4-ethylcyclohexyl)-, trans-

CC[C@@H]1CC[C@H](CC1)c1ccc(cc1)C(=O)O Request for Quotation
Chemical Name: Benzoic acid, 4-(4-ethylcyclohexyl)-, trans-
CAS Number: 87592-41-4
Product Number: AG008EOZ(AGN-PC-0VF2JX)
Synonyms:
MDL No:
Molecular Formula: C15H20O2
Molecular Weight: 232.3181

Identification/Properties

Computed Properties
Molecular Weight:
232.323g/mol
XLogP3:
4.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
232.146g/mol
Monoisotopic Mass:
232.146g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
246
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#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-((1R,4R)-4-Ethylcyclohexyl)benzoic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis for various applications. Within the realm of organic chemistry, this compound is coveted for its ability to serve as a key building block in the synthesis of more complex structures. Through strategic transformations and functional group manipulations, $name$ can be used to introduce specific structural motifs into target molecules, thereby diversifying the chemical landscape and enabling the creation of novel compounds with tailored properties. This compound's unique molecular structure, characterized by the presence of an ethylcyclohexyl group attached to a benzoic acid moiety, confers distinctive reactivity and steric properties that make it a valuable asset in organic synthesis strategies. By judiciously incorporating 4-((1R,4R)-4-Ethylcyclohexyl)benzoic acid into synthetic pathways, chemists can access a plethora of chemical space and unlock new avenues for drug discovery, materials science, and other innovative applications.