1. Home
  2. ethyl 4-[2-(4-hydroxypiperidin-1-yl)ethoxy]benzoate

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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 4-[2-(4-hydroxypiperidin-1-yl)ethoxy]benzoate

CCOC(=O)c1ccc(cc1)OCCN1CCC(CC1)O Request for Quotation
Chemical Name: ethyl 4-[2-(4-hydroxypiperidin-1-yl)ethoxy]benzoate
CAS Number: 937601-92-8
Product Number: AG00IHST(AGN-PC-01XG42)
Synonyms:
MDL No:
Molecular Formula: C16H23NO4
Molecular Weight: 293.3581

Identification/Properties

Computed Properties
Molecular Weight:
293.363g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
7
Exact Mass:
293.163g/mol
Monoisotopic Mass:
293.163g/mol
Topological Polar Surface Area:
59A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
307
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 4-(2-(4-hydroxypiperidin-1-yl)ethoxy)benzoate is a versatile compound widely used in chemical synthesis. Its primary application lies in its ability to serve as a key building block in the creation of pharmaceuticals and fine chemicals. This compound plays a crucial role in the development of various drugs due to its unique chemical structure and reactivity. By incorporating Ethyl 4-(2-(4-hydroxypiperidin-1-yl)ethoxy)benzoate into synthetic pathways, chemists can access a diverse range of molecular frameworks, enabling the synthesis of novel bioactive compounds with potential therapeutic applications. Additionally, the compound's functional groups provide opportunities for further derivatization, making it a valuable tool in the discovery and optimization of new chemical entities.