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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)-

L-Glutamic acid, N-[(phenylmethoxy)carbonyl]-, 5-ethyl ester

CCOC(=O)CC[C@@H](C(=O)O)NC(=O)OCc1ccccc1 Request for Quotation
Chemical Name: L-Glutamic acid, N-[(phenylmethoxy)carbonyl]-, 5-ethyl ester
CAS Number: 35726-62-6
Product Number: AG00C700(AGN-PC-0O99UY)
Synonyms:
MDL No:
Molecular Formula: C15H19NO6
Molecular Weight: 309.3145

Identification/Properties

Computed Properties
Molecular Weight:
309.318g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
10
Exact Mass:
309.121g/mol
Monoisotopic Mass:
309.121g/mol
Topological Polar Surface Area:
102A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
378
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-2-(((Benzyloxy)carbonyl)amino)-5-ethoxy-5-oxopentanoic acid, also known as $name$, plays a crucial role in chemical synthesis as a key intermediate compound. Within chemical synthesis, this compound is commonly utilized as a building block for the creation of complex organic molecules. Its exceptional properties make it a valuable tool in the development of various pharmaceuticals, agrochemicals, and other fine chemicals. In particular, its ability to undergo selective transformations and participate in diverse reactions makes it a versatile and indispensable component in the synthesis of biologically active compounds. By leveraging the unique structure of $name$, chemists can efficiently access a wide range of structurally complex molecules, paving the way for innovative advancements in synthetic chemistry.