856570-20-2

Basic information

• Product Name: s-2-CBz-3-pheylpropane-1-sulfonicacid
• Synonyms: s-2-CBz-3-pheylpropane-1-sulfonicacid;(S)-2-(Benzyloxycarbonylamino)-3-phenylpropane-1-sulfonic acid;(S)-2-Benzyl-3-(benzyloxy)-3-oxopropane-1-sulfonic acid;S-2-CBZ-3-Phenylpropane-1-sulfonic acid
• CAS NO: 856570-20-2
• Molecular Formula: C₁₇H₁₉NO₅S
• Molecular Weight: 349.405
• EINECS: -0
• Mol File: 856570-20-2.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Density: 1.325 g/cm³
• Refractive Index: 1.602
• CAS DataBase Reference: s-2-CBz-3-pheylpropane-1-sulfonicacid(CAS DataBase Reference)
• NIST Chemistry Reference: s-2-CBz-3-pheylpropane-1-sulfonicacid(856570-20-2)
• EPA Substance Registry System: s-2-CBz-3-pheylpropane-1-sulfonicacid(856570-20-2)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 856570-20-2(Hazardous Substances Data)

Usage

General Description

" S-2-CBz-3-phenylpropane-1-sulfonic acid" is a chemical compound that is a derivative of sulfonic acid. It contains a benzyl group attached to the second carbon and a phenyl group attached to the third carbon of the propane chain. s-2-CBz-3-pheylpropane-1-sulfonicacid has various industrial applications, including its use as a building block for the synthesis of pharmaceuticals, agrochemicals, and dyes. Its sulfonic acid functional group also makes it useful in the production of surfactants and detergents. Additionally, it can be used as a chiral auxiliary in asymmetric synthesis to control the stereochemistry of reactions.

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

• 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 
• 82001-62-5 (S)-2-<(benzyloxycarbonyl)amino>-3-phenylpropyl ethanethioate 

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 articles and documents

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

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.

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