1. Home
  2. 4-Piperidineacetic acid, 1-[(phenylmethoxy)carbonyl]-, ethyl ester

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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-Piperidineacetic acid, 1-[(phenylmethoxy)carbonyl]-, ethyl ester

CCOC(=O)CC1CCN(CC1)C(=O)OCc1ccccc1 Request for Quotation
Chemical Name: 4-Piperidineacetic acid, 1-[(phenylmethoxy)carbonyl]-, ethyl ester
CAS Number: 80221-26-7
Product Number: AG003QG0(AGN-PC-00K0IY)
Synonyms:
MDL No: MFCD09953323
Molecular Formula: C17H23NO4
Molecular Weight: 305.3688

Identification/Properties

Properties
BP:
416.1±28.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
305.374g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
305.163g/mol
Monoisotopic Mass:
305.163g/mol
Topological Polar Surface Area:
55.8A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
358
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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Ethyl N-Cbz-4-piperidineacetate is a versatile compound widely utilized in chemical synthesis for its valuable role as a protecting group in organic reactions. This compound is commonly employed in the field of organic chemistry to selectively shield specific functional groups within a molecule, thus facilitating the desired chemical transformations while preventing unwanted side reactions. By strategically incorporating Ethyl N-Cbz-4-piperidineacetate into synthesis pathways, chemists can control the reactivity of the molecule, enhance the yield of desired products, and streamline complex synthetic processes. This compound serves as a valuable tool in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals, making it an indispensable building block for advanced chemical research and development.