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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 1-Methyl-3-piperidinecarboxylate

CCOC(=O)C1CCCN(C1)C Request for Quotation
Chemical Name: Ethyl 1-Methyl-3-piperidinecarboxylate
CAS Number: 5166-67-6
Product Number: AG006UE4(AGN-PC-0WAD0V)
Synonyms:
MDL No:
Molecular Formula: C9H17NO2
Molecular Weight: 171.2368

Identification/Properties

Properties
BP:
211.1 °C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
171.24g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
171.126g/mol
Monoisotopic Mass:
171.126g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
159
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:
H227-H315-H319-H335
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 1-methyl-3-piperidinecarboxylate is commonly used as a key intermediate in organic chemical synthesis. Specifically, this compound is versatile in the development of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it a valuable building block for the creation of various complex molecules. In particular, Ethyl 1-methyl-3-piperidinecarboxylate is frequently employed in the synthesis of heterocyclic compounds, which play crucial roles in drug discovery and development. By incorporating this compound into chemical reactions, researchers can access a diverse array of functionalized compounds that possess significant biological activities. Additionally, Ethyl 1-methyl-3-piperidinecarboxylate serves as a valuable tool in structure-activity relationship studies, allowing scientists to tailor molecular structures for enhanced bioactivity and selectivity in drug design. Its use in chemical synthesis underscores its importance as a key component in the advancement of medicinal and agricultural chemistry.