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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-Acetamidopentanedioic acid

OC(=O)CCC(C(=O)O)NC(=O)C Request for Quotation
Chemical Name: 2-Acetamidopentanedioic acid
CAS Number: 5817-08-3
Product Number: AG00IACQ(AGN-PC-0WBO5R)
Synonyms:
MDL No: MFCD00063195
Molecular Formula: C7H11NO5
Molecular Weight: 189.1659

Identification/Properties

Computed Properties
Molecular Weight:
189.167g/mol
XLogP3:
-1.8
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
5
Exact Mass:
189.064g/mol
Monoisotopic Mass:
189.064g/mol
Topological Polar Surface Area:
104A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
225
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


2-Acetamidopentanedioic acid, also known as N-acetylglutamic acid, plays a significant role in chemical synthesis as a versatile intermediate. This compound serves as a crucial building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. With its unique structure and functional groups, 2-Acetamidopentanedioic acid can undergo a range of chemical reactions, including acylation, amidation, and esterification, allowing for the synthesis of complex organic molecules. In addition, this compound is employed in peptide synthesis as a protecting group for amino acids, enabling precise control over the formation of peptide bonds. Its utility in chemical synthesis extends to the development of innovative materials, bioactive compounds, and synthetic intermediates, making it a valuable tool for researchers and industry professionals alike.