N-AcetyI-L-Tryptophan 丨CAS 1218-34-4

N-AcetyI-L-Tryptophan 丨CAS 1218-34-4
Product Introduction:
CAS No.: 1218-34-4
Product Name: N-AcetyI-L-Tryptophan
Grade: AJI
Molecular Formula: C13H14N2O3
Molecular Weight: 246.26
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Technical Parameters
Description

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Bulk Quantity N-AcetyI-L-Tryptophan 丨CAS 1218-34-4

 

N-Acetyl-L-Tryptophan is an acetylated derivative of L-tryptophan, an aromatic amino acid characterized by its indole ring structure. The addition of an acetyl group modifies the amino functionality while retaining the compound's characteristic tryptophan framework. This combination of structural features makes N-Acetyl-L-Tryptophan relevant to amino acid research, biochemical studies, and the synthesis of specialized organic compounds.

 

Chemical Identifiers

 

InChI InChI=1S/C13H14N2O3/c1-8(16)15-12(13(17)18)6-9-7-14-11-5-3-2-4-10(9)11/h2-5,7,12,14H,6H2,1H3,(H,15,16)(H,17,18)/t12-/m0/s1
InChI Key DZTHIGRZJZPRDV-LBPRGKRZSA-N
Smiles CC(=O)N[C@@H](CC1=CNC2=CC=CC=C21)C(=O)O
EC No. 214-935-9
MDL No. MFCD00065976
PubChem CID 700653

 

 

 

Applications

 

Pharmaceutical Research and Drug Discovery

Modified amino acids are useful research compounds in medicinal chemistry because changes to functional groups can influence molecular interactions and chemical behavior. N-Acetyl-L-Tryptophan may serve as a research material or synthetic intermediate in studies involving tryptophan derivatives and other indole-containing compounds. Its suitability for a particular pharmaceutical research pathway depends on the target structure and validated synthetic approach.

Biochemical and Metabolic Research

Tryptophan is an important amino acid investigated in protein chemistry, metabolism, and molecular interactions. N-Acetyl-L-Tryptophan can support research examining modified amino acids, the influence of N-acetylation on molecular properties, and the behavior of tryptophan derivatives in defined experimental systems. Its application depends on the specific biochemical question and research model.

Organic Synthesis and Indole Chemistry

The indole ring is an important structural feature in organic synthesis and the development of nitrogen-containing compounds. N-Acetyl-L-Tryptophan provides an aromatic amino acid framework with an acetyl-modified nitrogen group that may be relevant to selected synthetic transformations. It can support research into functionalized tryptophan derivatives and specialized intermediates, depending on reaction compatibility and the intended product.

Analytical Chemistry and Reference Research

Structurally defined amino acid derivatives can be useful in analytical method development and compound characterization. N-Acetyl-L-Tryptophan may be used in suitable analytical workflows to investigate identity, purity, stability, and the behavior of acetylated amino acid derivatives. Applications requiring reference-standard performance should be supported by appropriate characterization and quality documentation.

 

 

 

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