4-O-benzyl 2-O-ethyl morpholine-2,4-dicarboxylate


Chemical Name: 4-O-benzyl 2-O-ethyl morpholine-2,4-dicarboxylate
CAS Number: 1226776-83-5
Product Number: AG0017LL(AGN-PC-0BHSE7)
Synonyms:
MDL No: MFCD16495879
Molecular Formula: C15H19NO5
Molecular Weight: 293.3151

Identification/Properties


Properties
BP:
411.9±45.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
293.319g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
6
Exact Mass:
293.126g/mol
Monoisotopic Mass:
293.126g/mol
Topological Polar Surface Area:
65.1A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
354
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


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



Ethyl N-Cbz-morpholine-2-carboxylate is a versatile compound that finds wide application in chemical synthesis. It serves as a key building block in the creation of various complex organic molecules. This compound is commonly used in the pharmaceutical industry for the synthesis of potential drug candidates due to its ability to introduce the Cbz protecting group into molecules, which helps in controlling reactivity and selectivity during subsequent reactions. Additionally, Ethyl N-Cbz-morpholine-2-carboxylate can be utilized in the preparation of bioactive compounds, agrochemicals, and materials with specific properties. Its unique structural features and reactivity make it an essential reagent for the efficient and selective synthesis of a diverse range of molecules in organic chemistry.