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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)-

2-Morpholinecarboxylic acid, 4-(phenylmethyl)-, ethyl ester

CCOC(=O)C1OCCN(C1)Cc1ccccc1 Request for Quotation
Chemical Name: 2-Morpholinecarboxylic acid, 4-(phenylmethyl)-, ethyl ester
CAS Number: 135072-32-1
Product Number: AG003Q9S(AGN-PC-09CV7I)
Synonyms:
MDL No: MFCD14584462
Molecular Formula: C14H19NO3
Molecular Weight: 249.3056

Identification/Properties

Properties
BP:
140 - 150 °C at 0.1 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Liquid
Computed Properties
Molecular Weight:
249.31g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
249.136g/mol
Monoisotopic Mass:
249.136g/mol
Topological Polar Surface Area:
38.8A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
264
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 4-benzylmorpholine-2-carboxylate is a versatile compound commonly used in chemical synthesis. This compound serves as a crucial building block in the creation of various pharmaceuticals and organic compounds due to its unique structure and reactivity.In chemical synthesis, Ethyl 4-benzylmorpholine-2-carboxylate can be utilized as a key intermediate in the production of diverse pharmacological agents. Its benzylmorpholine moiety enables the compound to participate in various reactions, such as acylations, reductions, and cyclizations, leading to the formation of complex molecular structures with desired biological activities.Furthermore, the ethyl ester group in Ethyl 4-benzylmorpholine-2-carboxylate provides flexibility for further modifications, allowing chemists to tailor the compound for specific applications. By incorporating this compound into synthetic pathways, researchers can access a wide range of derivatives with potential therapeutic benefits.Overall, Ethyl 4-benzylmorpholine-2-carboxylate plays a pivotal role in advancing chemical synthesis by offering a strategic entry point for the construction of intricate molecules with pharmaceutical relevance.