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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 2-methyl-2-piperidin-4-ylpropanoate

CCOC(=O)C(C1CCNCC1)(C)C.Cl Request for Quotation
Chemical Name: ethyl 2-methyl-2-piperidin-4-ylpropanoate
CAS Number: 243836-26-2
Product Number: AG0037RQ(AGN-PC-086EQX)
Synonyms:
MDL No:
Molecular Formula: C11H22ClNO2
Molecular Weight: 235.7509

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
235.752g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
235.134g/mol
Monoisotopic Mass:
235.134g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
196
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:
2
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


Ethyl 2-methyl-2-(piperidin-4-yl)propanoate hydrochloride is a versatile compound that finds a crucial role in chemical synthesis processes. This compound serves as an important intermediate in the synthesis of various pharmaceuticals and organic molecules. Its unique structure containing a piperidine ring provides it with the ability to participate in a wide range of reactions, allowing for the creation of complex molecular structures. Additionally, the hydrochloride salt form enhances the compound's solubility in aqueous solutions, making it easier to work with in wet chemistry processes. Researchers and chemists often utilize ethyl 2-methyl-2-(piperidin-4-yl)propanoate hydrochloride as a key building block in the development of new drugs, agrochemicals, and materials due to its synthetic versatility and functional properties.