4S)-2-(1-((R)-2-Amino-2-(4-hydroxyphenyl)acetamido)-2-(((1R)-2-((carboxy((4S)-4-carboxy-5,5-dimethylthiazolidin-2-yl)methyl)amino)-1-(4-hydroxyphenyl)-2-oxoethyl)amino)-2-oxoethyl)-5,5-dimethylthiazolidine-4-carboxylic acid

95%

Reagent Code: #232812
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CAS Number 2088961-38-8

science Other reagents with same CAS 2088961-38-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 748.82 g/mol
Formula C₃₂H₄₀N₆O₁₁S₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in the synthesis of certain beta-lactam antibiotics, particularly as an intermediate in the production of semisynthetic penicillins and cephalosporins. Its structure supports the formation of key pharmacophores that enhance antimicrobial activity and resistance to beta-lactamase enzymes. Commonly employed in pharmaceutical research for developing antibiotics with improved stability and spectrum of action. Also utilized in peptide coupling reactions due to its functional carboxylic acid and amino groups, enabling conjugation to other bioactive molecules.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿160,000.00
4S)-2-(1-((R)-2-Amino-2-(4-hydroxyphenyl)acetamido)-2-(((1R)-2-((carboxy((4S)-4-carboxy-5,5-dimethylthiazolidin-2-yl)methyl)amino)-1-(4-hydroxyphenyl)-2-oxoethyl)amino)-2-oxoethyl)-5,5-dimethylthiazolidine-4-carboxylic acid
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Used in the synthesis of certain beta-lactam antibiotics, particularly as an intermediate in the production of semisynthetic penicillins and cephalosporins. Its structure supports the formation of key pharmacophores that enhance antimicrobial activity and resistance to beta-lactamase enzymes. Commonly employed in pharmaceutical research for developing antibiotics with improved stability and spectrum of action. Also utilized in peptide coupling reactions due to its functional carboxylic acid and amino groups, enabling conjugation to other bioactive molecules.
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