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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)-

(R)-4-benzyl-5-oxomorpholine-3-carboxylic acid methyl ester

COC(=O)[C@@H]1COCC(=O)N1Cc1ccccc1 Request for Quotation
Chemical Name: (R)-4-benzyl-5-oxomorpholine-3-carboxylic acid methyl ester
CAS Number: 1235181-00-6
Product Number: AG000KPS(AGN-PC-0O0NP3)
Synonyms:
MDL No: MFCD12031314
Molecular Formula: C13H15NO4
Molecular Weight: 249.2625

Identification/Properties

Properties
BP:
423.0±45.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
249.266g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
249.1g/mol
Monoisotopic Mass:
249.1g/mol
Topological Polar Surface Area:
55.8A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
312
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl (S)-4-Benzyl-5-oxomorpholine-3-carboxylate is a versatile compound that finds widespread applications in chemical synthesis, particularly in the pharmaceutical and agrochemical industries. This compound serves as a key building block for the synthesis of various biologically active molecules and can be used in the creation of novel pharmaceuticals, pesticides, and other valuable compounds. Its unique structure and functional groups allow for strategic modifications, enabling chemists to design and synthesize complex molecules with specific biological activities. In chemical synthesis, Methyl (S)-4-Benzyl-5-oxomorpholine-3-carboxylate plays a crucial role as a chiral intermediate, providing a platform for the development of stereochemically pure compounds with enhanced biological properties. Its incorporation into synthetic routes allows for the efficient construction of diverse molecular scaffolds and the exploration of new avenues in drug discovery and development.