L-Alanine allyl ester p-toluenesulfonate
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L-Alanine allyl ester p-toluenesulfonate

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Category
L-Amino Acids
Catalog number
BAT-002151
CAS number
20845-17-4
Molecular Formula
C13H19NO5S
Molecular Weight
301.36
IUPAC Name
4-methylbenzenesulfonic acid;prop-2-enyl (2S)-2-aminopropanoate
Synonyms
H-Ala-Oallyl.TsOH; L-alanine allyl ester tosylic acid; (S)-Allyl 2-aminopropanoate 4-methylbenzenesulfonate; H-Ala-allyl ester p-tosylate; L-Alanine, 2-propenyl ester, 4-methylbenzenesulfonate; Allyl L-alaninate 4-methylbenzenesulfonate (1:1); H-Ala-allyl ester p-tosylate
Related CAS
44812-81-9 (free base)
Appearance
White Powder
Purity
≥95%
Storage
Store at RT
InChI
InChI=1S/C7H8O3S.C6H11NO2/c1-6-2-4-7(5-3-6)11(8,9)10;1-3-4-9-6(8)5(2)7/h2-5H,1H3,(H,8,9,10);3,5H,1,4,7H2,2H3/t;5-/m.0/s1
InChI Key
PXNUQOZOYKVNEI-ZSCHJXSPSA-N
Canonical SMILES
CC1=CC=C(C=C1)S(=O)(=O)O.CC(C(=O)OCC=C)N

L-Alanine allyl ester p-toluenesulfonate, a chemical compound crucial for chemical synthesis and research, plays a pivotal role in various applications. Here are the key applications presented with high perplexity and burstiness:

Peptide Synthesis: Acting as an intermediary in peptide synthesis, L-Alanine allyl ester p-toluenesulfonate contributes to the construction of peptide chains through its ester functional group. This versatile compound seamlessly integrates into developing peptide structures, functioning as a fundamental building block. Its involvement streamlines the production of peptides, vital for diverse research endeavors spanning multiple biological and medical domains.

Organic Synthesis: Renowned for its significance in organic chemistry, this compound serves as a valuable reagent in crafting intricate molecules. The allyl ester group's adaptability enables a spectrum of reactions, including allylic substitution and cross-coupling, facilitating the incorporation of functional groups and the assembly of complex molecular architectures. Chemists rely on its versatility as a cornerstone reagent for pioneering advancements in novel organic compound synthesis.

Drug Discovery: Within the realm of pharmaceutical innovation, L-Alanine allyl ester p-toluenesulfonate plays a pivotal role in designing and synthesizing novel drug candidates. Its inherent structural characteristics offer avenues for tailored modifications that can culminate in the development of active pharmaceutical ingredients (APIs). Serving as a foundational scaffold, this compound can be tailored to elicit specific biological activities, catalyzing advancements in drug discovery research.

Catalysis Research: In catalysis research, this compound assumes the role of a substrate or ligand within catalytic systems, contributing to the exploration of reaction mechanisms and the evolution of innovative catalytic processes. Leveraging its chemical properties, researchers scrutinize reaction dynamics and pioneer novel catalytic approaches, fostering the development of highly efficient and selective catalytic systems. The compound's reactive nature fuels groundbreaking strides in catalytic chemistry, propelling the creation of cutting-edge catalysts.

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