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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)-

1-[2-Amino-1-(4-methoxyphenyl)ethyl]cyclohexanol

NCC(C1(O)CCCCC1)c1ccc(cc1)OC Request for Quotation
Chemical Name: 1-[2-Amino-1-(4-methoxyphenyl)ethyl]cyclohexanol
CAS Number: 93413-77-5
Product Number: AG00IKEM(AGN-PC-0WALW5)
Synonyms:
MDL No:
Molecular Formula: C15H23NO2
Molecular Weight: 249.3486

Identification/Properties

Computed Properties
Molecular Weight:
249.354g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
249.173g/mol
Monoisotopic Mass:
249.173g/mol
Topological Polar Surface Area:
55.5A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
243
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The chemical compound 1-(2-Amino-1-(4-methoxyphenyl)ethyl)cyclohexanol plays a crucial role in chemical synthesis as a versatile building block. Its unique structure combines an amino group, a methoxyphenyl moiety, and a cyclohexanol ring, allowing for diverse reactivity and functional group compatibility. This compound is commonly utilized as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its amino group serves as a crucial site for further derivatization, enabling the introduction of different functional groups or scaffolds. Additionally, the cyclohexanol ring provides a stereochemically favorable framework for the construction of complex molecules. By incorporating 1-(2-Amino-1-(4-methoxyphenyl)ethyl)cyclohexanol into synthetic routes, chemists can access a wide array of compounds with tailored properties and biological activities.