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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)-

ethyl 6-phenylpiperidine-2-carboxylate

CCOC(=O)C1CCCC(N1)c1ccccc1 Request for Quotation
Chemical Name: ethyl 6-phenylpiperidine-2-carboxylate
CAS Number: 1137664-24-4
Product Number: AG0009LN(AGN-PC-04Q6LT)
Synonyms:
MDL No: MFCD06410519
Molecular Formula: C14H19NO2
Molecular Weight: 233.3062

Identification/Properties

Computed Properties
Molecular Weight:
233.311g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
233.142g/mol
Monoisotopic Mass:
233.142g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
249
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 6-phenylpiperidine-2-carboxylate is a versatile chemical compound that finds wide application in chemical synthesis processes. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and other fine chemicals. Due to its unique structure and reactivity, Ethyl 6-phenylpiperidine-2-carboxylate is particularly valuable in the synthesis of complex molecules with biological activity.In organic synthesis, this compound can be used as a precursor in the formation of different heterocyclic compounds, which are commonly found in drug molecules. Its incorporation into the molecular structure can often enhance the biological properties of the resulting compounds, making it a valuable tool for medicinal chemists.Additionally, Ethyl 6-phenylpiperidine-2-carboxylate can participate in various functional group transformations and substitution reactions, allowing for the introduction of diverse chemical functionalities into target molecules. This versatility makes it an indispensable reagent in the synthesis of a wide range of organic compounds with desirable properties for pharmaceutical and agrochemical applications.Overall, the application of Ethyl 6-phenylpiperidine-2-carboxylate in chemical synthesis plays a crucial role in the development of novel compounds with potential therapeutic or agricultural benefits. Its strategic use as a synthetic intermediate enables the efficient and targeted construction of complex molecules, contributing to advancements in the field of organic chemistry.