N-Acetyl-L-Glutamine


Chemical Name: N-Acetyl-L-Glutamine
CAS Number: 35305-74-9
Product Number: AG00ILLT(AGN-PC-0WAEF8)
Synonyms:
MDL No:
Molecular Formula: C7H12N2O4
Molecular Weight: 188.1812

Identification/Properties


Properties
MP:
206-208 °C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
188.183g/mol
XLogP3:
-1.4
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
188.08g/mol
Monoisotopic Mass:
188.08g/mol
Topological Polar Surface Area:
110A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
227
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



The (S)-5-Acetamido-2-amino-5-oxopentanoic acid, also known as $name$, plays a crucial role in chemical synthesis as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. This compound serves as a versatile building block in organic chemistry, enabling the creation of complex molecular structures with specific stereochemical configurations.In chemical synthesis, (S)-5-Acetamido-2-amino-5-oxopentanoic acid is commonly utilized to introduce functional groups, modify molecular backbones, and facilitate the formation of peptide bonds. Its unique structure and reactivity make it an invaluable tool for the creation of peptide-based drugs, amino acid derivatives, and other biologically active compounds.By incorporating (S)-5-Acetamido-2-amino-5-oxopentanoic acid into synthetic pathways, chemists can access a diverse array of chemistries and transformations, allowing for the tailored design and construction of target molecules with high precision and efficiency. Its role as a chiral amino acid derivative further enhances its utility in asymmetric synthesis, enabling the selective formation of enantiomerically pure compounds with enhanced biological activity and pharmacological properties.Overall, the application of (S)-5-Acetamido-2-amino-5-oxopentanoic acid in chemical synthesis offers a powerful tool for the strategic design and synthesis of complex molecules with significant implications in drug discovery, materials science, and chemical research.