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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)-

Glycine, N-(1-oxopentyl)-

CCCCC(=O)NCC(=O)O Request for Quotation
Chemical Name: Glycine, N-(1-oxopentyl)-
CAS Number: 24003-66-5
Product Number: AG003S7I(AGN-PC-0LGFFV)
Synonyms:
MDL No:
Molecular Formula: C7H13NO3
Molecular Weight: 159.1830

Identification/Properties

Properties
MP:
77-79ºC
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
159.185g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
159.09g/mol
Monoisotopic Mass:
159.09g/mol
Topological Polar Surface Area:
66.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
145
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Pentanamidoacetic acid, also known as N-(2-aminopentanoyl)glycine, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, 2-Pentanamidoacetic acid can be utilized as a key starting material for the synthesis of peptides, which are essential components in drug development and biological research. By incorporating this compound into peptide synthesis reactions, chemists can introduce specific functionalities and structural motifs into the peptide chain, leading to the creation of novel bioactive molecules with potential therapeutic applications.Furthermore, 2-Pentanamidoacetic acid can serve as a precursor for the synthesis of complex organic molecules, such as amino acid derivatives and heterocyclic compounds. Its functional groups and chiral centers enable chemists to introduce stereochemistry and molecular diversity into their target molecules, allowing for the creation of structurally diverse and biologically active compounds.Overall, the application of 2-Pentanamidoacetic acid in chemical synthesis offers a wide range of opportunities for the development of pharmaceuticals, agrochemicals, and other valuable chemical products. Its versatility and potential for modification make it a valuable tool for synthetic chemists seeking to access new and innovative compounds through strategic molecular manipulations.