1008531-03-0

Basic information

• Product Name: Methyl (2S)-2-hydroxy-3-{N-[4-(4-methylphenoxy)phenyl]-N-methanesulfonylamino}propionate
• Synonyms: Methyl (2S)-2-hydroxy-3-{N-[4-(4-methylphenoxy)phenyl]-N-methanesulfonylamino}propionate
• CAS NO: 1008531-03-0
• Molecular Weight: 379.434
• Mol File: 1008531-03-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Methyl (2S)-2-hydroxy-3-{N-[4-(4-methylphenoxy)phenyl]-N-methanesulfonylamino}propionate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl (2S)-2-hydroxy-3-{N-[4-(4-methylphenoxy)phenyl]-N-methanesulfonylamino}propionate(1008531-03-0)
• EPA Substance Registry System: Methyl (2S)-2-hydroxy-3-{N-[4-(4-methylphenoxy)phenyl]-N-methanesulfonylamino}propionate(1008531-03-0)

Safety Data

• Hazardous Substances Data: 1008531-03-0(Hazardous Substances Data)

Upstream product

• 1008530-98-0 N-[4-(4-trifluoromethylphenoxy)phenyl]methanesulfonamide 
• 4538-50-5 methyl (2S)-glycidate 
• 1017800-01-9 N-[4-(4-methylphenoxy)phenyl]methane sulfonamide 

Downstream Products

• 1018434-15-5 Methyl (2S)-2-methoxy-3-{N-[4-(4-methylphenoxy)phenyl]-N-methanesulfonylamino}propionate 
• 1043878-22-3 C₁₉H₂₀F₃NO₈S₂ 
• 1016987-22-6 C₁₇H₁₉NO₆S 

Relevant articles and documents

Microwave assisted ring-opening of epoxides with N-biaryl sulfonamides in the synthesis of matrix metalloproteinase-9 inhibitors

A microwave accelerated epoxide ring-opening process with N-biaryl sulfonamides is described. Under this mild, highly efficient condition, an α-hydroxy-β-N-biaryl sulfonamide skeleton is rapidly assembled leading ultimately to a novel series of matrix met

β-N-Biaryl ether sulfonamide hydroxamates as potent gelatinase inhibitors: Part 2. Optimization of α-amino substituents

The introduction and the optimization of an α-amino substituent based on a series of α-hydroxy-β-N-biaryl ether sulfonamide hydroxamates is described. The modification leads to a new series of MMP-2/MMP-9 inhibitors with enhanced inhibitory activities and