2-Amino-3-methyl-3-sulfino-4-(1H-1,2,3-triazol-1-yl)butanoic acid

98%

Reagent Code: #78596
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CAS Number 118175-11-4

science Other reagents with same CAS 118175-11-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.26 g/mol
Formula C₇H₁₂N₄O₄S
badge Registry Numbers
MDL Number MFCD13191753
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This chemical is primarily utilized in biochemical research and pharmaceutical development due to its unique structure, which combines amino, sulfino, and triazole functional groups. It serves as a precursor or intermediate in the synthesis of more complex molecules, particularly those targeting enzyme inhibition or receptor modulation. Its triazole moiety makes it valuable in designing compounds with potential antimicrobial or antiviral properties. Additionally, it is explored in peptide chemistry for creating modified amino acids that can enhance the stability or activity of therapeutic peptides. Its sulfino group also contributes to its role in studies involving redox reactions and sulfur metabolism.

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Test Parameter Specification
Appearance Off-White Powder
Purity (%) 97.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿85,149.00
inventory 100mg
10-20 days ฿56,772.00

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2-Amino-3-methyl-3-sulfino-4-(1H-1,2,3-triazol-1-yl)butanoic acid
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This chemical is primarily utilized in biochemical research and pharmaceutical development due to its unique structure, which combines amino, sulfino, and triazole functional groups. It serves as a precursor or intermediate in the synthesis of more complex molecules, particularly those targeting enzyme inhibition or receptor modulation. Its triazole moiety makes it valuable in designing compounds with potential antimicrobial or antiviral properties. Additionally, it is explored in peptide chemistry for c

This chemical is primarily utilized in biochemical research and pharmaceutical development due to its unique structure, which combines amino, sulfino, and triazole functional groups. It serves as a precursor or intermediate in the synthesis of more complex molecules, particularly those targeting enzyme inhibition or receptor modulation. Its triazole moiety makes it valuable in designing compounds with potential antimicrobial or antiviral properties. Additionally, it is explored in peptide chemistry for creating modified amino acids that can enhance the stability or activity of therapeutic peptides. Its sulfino group also contributes to its role in studies involving redox reactions and sulfur metabolism.

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