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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)-

(4-cyclopentylphenyl)methanol

OCc1ccc(cc1)C1CCCC1 Request for Quotation
Chemical Name: (4-cyclopentylphenyl)methanol
CAS Number: 171623-29-3
Product Number: AG00AO7S(AGN-PC-0HLB2D)
Synonyms:
MDL No:
Molecular Formula: C12H16O
Molecular Weight: 176.2548

Identification/Properties

Computed Properties
Molecular Weight:
176.25g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
176.120115g/mol
Monoisotopic Mass:
176.120115g/mol
Topological Polar Surface Area:
20.2Ų
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
141
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


(4-Cyclopentylphenyl)methanol, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role as a building block in various organic reactions, offering a range of applications in the field of chemistry. Its unique structure and reactivity make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.One of the key applications of (4-Cyclopentylphenyl)methanol is as a starting material for the synthesis of novel molecules with specific properties. Its cyclopentyl ring and phenyl group provide a diverse set of functional groups that can be modified to tailor the compound for desired chemical reactions. This compound serves as a pivotal component in the creation of complex organic molecules, serving as a precursor for a variety of chemical transformations.Furthermore, (4-Cyclopentylphenyl)methanol is utilized in the preparation of chiral compounds due to its chirality-inducing properties. By incorporating this compound into asymmetric synthesis, chemists can selectively form enantiomerically enriched products, crucial in pharmaceutical development and materials science.Overall, (4-Cyclopentylphenyl)methanol is a valuable tool in the hands of synthetic chemists, enabling the creation of diverse chemical structures with tailored properties. Its applications span across a wide range of industries, making it an indispensable building block in modern chemical synthesis.