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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-Piperidinecarboxylic acid, 1-(chloroacetyl)-, ethyl ester

CCOC(=O)C1CCN(CC1)C(=O)CCl Request for Quotation
Chemical Name: 4-Piperidinecarboxylic acid, 1-(chloroacetyl)-, ethyl ester
CAS Number: 318280-71-6
Product Number: AG00BYH4(AGN-PC-0JVOK2)
Synonyms:
MDL No:
Molecular Formula: C10H16ClNO3
Molecular Weight: 233.6919

Identification/Properties

Properties
BP:
345.8°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
233.692g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
233.082g/mol
Monoisotopic Mass:
233.082g/mol
Topological Polar Surface Area:
46.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
237
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 1-(2-chloroacetyl)piperidine-4-carboxylate, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis for various applications. This compound serves as a crucial building block in the production of complex organic molecules due to its unique chemical properties.One of the primary applications of Ethyl 1-(2-chloroacetyl)piperidine-4-carboxylate is in the synthesis of pharmaceutical compounds. By incorporating this compound into the synthesis process, chemists can efficiently create new drug candidates with potential therapeutic benefits. The presence of the piperidine ring in the structure of Ethyl 1-(2-chloroacetyl)piperidine-4-carboxylate enhances its pharmacological properties and makes it a valuable intermediate in pharmaceutical research and development.Furthermore, Ethyl 1-(2-chloroacetyl)piperidine-4-carboxylate is also utilized in the field of agrochemicals for the production of pesticides and herbicides. Its chemical structure enables the synthesis of active ingredients that exhibit specific biological activities against pests and weeds, making it an essential component in the formulation of agricultural products.Overall, the application of Ethyl 1-(2-chloroacetyl)piperidine-4-carboxylate in chemical synthesis extends across various industries, highlighting its significance as a key intermediate for the creation of diverse organic compounds with targeted functionalities.