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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-[4-(methylamino)benzoyl]-, diethyl ester

CCOC(=O)[C@@H](NC(=O)c1ccc(cc1)NC)CCC(=O)OCC Request for Quotation
Chemical Name: L-Glutamic acid, N-[4-(methylamino)benzoyl]-, diethyl ester
CAS Number: 2378-95-2
Product Number: AG00C3VB(AGN-PC-0O84GU)
Synonyms:
MDL No:
Molecular Formula: C17H24N2O5
Molecular Weight: 336.3829

Identification/Properties

Computed Properties
Molecular Weight:
336.388g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
11
Exact Mass:
336.169g/mol
Monoisotopic Mass:
336.169g/mol
Topological Polar Surface Area:
93.7A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
419
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


(S)-Diethyl 2-(4-(methylamino)benzamido)pentanedioate is a versatile compound widely used in chemical synthesis as a chiral building block. Its unique structure offers a variety of applications in the preparation of pharmaceuticals, agrochemicals, and biologically active molecules. This compound serves as a key intermediate in the synthesis of complex organic molecules, allowing chemists to access enantiomerically pure compounds that are crucial for drug development and medicinal chemistry research. By leveraging the chiral nature of this compound, chemists can achieve precise control over the stereochemistry of their target molecules, paving the way for the creation of novel compounds with enhanced pharmacological properties and biological activity.