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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-(trans-4-propylcyclohexyl)-

CCC[C@@H]1CC[C@H](CC1)c1ccc(cc1)C(=O)O Request for Quotation
Chemical Name: Benzoic acid, 4-(trans-4-propylcyclohexyl)-
CAS Number: 65355-29-5
Product Number: AG003UXJ(AGN-PC-0OF7IR)
Synonyms:
MDL No: MFCD06658177
Molecular Formula: C16H22O2
Molecular Weight: 246.3447

Identification/Properties

Properties
MP:
206°C(lit.)
BP:
383.7°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
246.35g/mol
XLogP3:
5.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
4
Exact Mass:
246.162g/mol
Monoisotopic Mass:
246.162g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
258
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 4-(trans-4-n-Propylcyclohexyl)benzoic acid is a valuable compound commonly used in chemical synthesis as a versatile building block. This compound serves as an important intermediate in the synthesis of various organic molecules due to its unique structure and reactivity. Its applications range from pharmaceuticals to materials science, where it can be utilized to introduce specific functionalities or structural motifs into complex molecules. In particular, this compound's ability to undergo various chemical transformations, such as esterification, amidation, or even oxidation, makes it a valuable tool in the hands of synthetic chemists looking to create novel compounds for different applications. Due to its stability and compatibility with a wide range of reaction conditions, 4-(trans-4-n-Propylcyclohexyl)benzoic acid has become a staple reagent in the toolbox of organic chemists seeking to design and synthesize new molecules with tailored properties.