856570-20-2

Usage

Uses

Used in Pharmaceutical Industry:
s-2-CBz-3-phenylpropane-1-sulfonic acid is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its structural properties allow for the creation of diverse chemical entities with potential medicinal applications.
Used in Agrochemical Industry:
In the agrochemical sector, s-2-CBz-3-phenylpropane-1-sulfonic acid serves as a key component in the synthesis of various agrochemicals, such as pesticides and herbicides. Its incorporation into these products enhances their effectiveness in protecting crops and managing pests.
Used in Dye Industry:
s-2-CBz-3-phenylpropane-1-sulfonic acid is utilized in the production of dyes, where its chemical structure imparts color and stability to the final products. This makes it a valuable component in the formulation of dyes for various applications, including textiles, plastics, and printing inks.
Used in Surfactant and Detergent Production:
The sulfonic acid functional group present in s-2-CBz-3-phenylpropane-1-sulfonic acid makes it an effective ingredient in the manufacturing of surfactants and detergents. Its inclusion in these products enhances their cleaning and emulsifying properties, making them more efficient in various cleaning applications.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
s-2-CBz-3-phenylpropane-1-sulfonic acid is employed as a chiral auxiliary in asymmetric synthesis to control the stereochemistry of chemical reactions. Its unique structure allows for the selective formation of desired enantiomers, which is crucial in the synthesis of enantioselective compounds with specific biological activities.

InChI:InChI=1/C17H19NO5S/c19-17(23-12-15-9-5-2-6-10-15)18-16(13-24(20,21)22)11-14-7-3-1-4-8-14/h1-10,16H,11-13H2,(H,18,19)(H,20,21,22)/t16-/m0/s1

Upstream product

• 82001-62-5 (S)-2-<(benzyloxycarbonyl)amino>-3-phenylpropyl ethanethioate 
• 135731-20-3 (S)-2-{[(benzyloxy)carbonyl]amino}-3-phenylpropyl methanesulfonate 
• 41518-17-6 Z-Phe-O-COO-isoBu 
• 6372-14-1 N-((benzyloxy)carbonyl)-L-phenylalaninol 
• 1161-13-3 N-Cbz-L-Phe 
• 126301-32-4 (S)-2-amino-3-phenylpropane-1-sulfonic acid 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 1169199-24-9 Cbz-Phe-ψ[CH2SO2]-F 
• 1169199-29-4 Cbz-Phe-ψ[CH2SO2NH]-β-Ala-ψ[CH2SO2]-F 
• 1300689-96-6 L-Phe-[CH₂SO₂]-FHCl 
• 1206530-78-0 (S)-(2-benzyloxycarbonylamino-3-phenyl)propanesulfonamide 
• 849949-24-2 Cbz-Phe-ψ[CH2SO2]-N3 

Relevant academic research and scientific papers

Facile synthesis of hybrid sulfonophosphinodipeptides composing of taurines and 1-aminoalkylphosphinic acids

Both sulfonopeptides and phosphonopeptides are important analogs of naturally occurring peptides and have been widely used as enzyme inhibitors and haptens for producing catalytic antibodies due to their tetrahedrally structural features. A series of hybr

Synthesis and biological evaluation of novel irreversible serine protease inhibitors using amino acid based sulfonyl fluorides as an electrophilic trap

We have designed and synthesized novel irreversible serine protease inhibitors containing aliphatic sulfonyl fluorides as an electrophilic trap. These substituted taurine sulfonyl fluorides derived from taurine or protected amino acids were conveniently s

A simple synthesis of N β-Fmoc/Z-amino alkyl thiols and their use in the synthesis of N β-Fmoc/Z-amino alkyl sulfonic acids

A simple and efficient protocol for the synthesis of Nβ- Fmoc/Z-amino alkyl thiols is described. The approach uses sodium pyrosulfite-mediated hydrolysis of isothiouronium salts resulting from the reaction between N-protected aminoalkyl iodides and thiourea. N-Protected taurines were prepared through performic acid oxidation of the thiols and the products were further utilized for the synthesis of dipeptidosulfonamides. Georg Thieme Verlag Stuttgart - New York.

First and convergent synthesis of hybrid sulfonophosphinopeptides

Figure Presented Hybrid sulfonophosphinopeptides were first and convergently synthesized in satisfactory to good yields via the Mannich-type reaction of N-protected 2-aminoalkanesulfonamides, aromatic aldehydes, and aryldichlorophosphines and subsequent aminolysis with amino esters.

Synthesis and applications of β-aminoethanesulfonyl azides

A very efficient method for the synthesis of β-aminoethanesulfonyl azides is descibed. These aliphatic sulfonyl azides are accessible starting from a variety of protected amino acids, including those having functionalized side chains. Furthermore, these s

An efficient synthesis of N-protected β-aminoethanesulfonyl chlorides: Versatile building blocks for the synthesis of oligopeptidosulfonamides

A very efficient method for the synthesis of β-aminoethanesulfonyl chlorides is described. These aliphatic functionalized sulfonyl chlorides are accessible starting from a variety of protected amino acids, including those having functionalized side chains