(6R,7R)-3-(Chloromethyl)-8-oxo-7-[[2-(2-thienyl)acetyl]amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid (4-Methoxyphenyl)methyl Ester

95%

Reagent Code: #231025
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CAS Number 101182-25-6

science Other reagents with same CAS 101182-25-6

blur_circular Chemical Specifications

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Weight 402.99 g/mol
Formula C₂₂H₂₁ClN₂O₅S₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of certain cephalosporin antibiotics. The compound plays a key role in the production of semi-synthetic beta-lactam antibiotics, particularly those designed to resist degradation by bacterial enzymes. Its structure allows for modification at key positions to enhance antimicrobial activity, improve pharmacokinetics, or increase stability against beta-lactamases. Commonly employed in pharmaceutical manufacturing to develop broad-spectrum antibiotics effective against both gram-positive and gram-negative bacteria.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿20,160.00
inventory 100mg
10-20 days ฿37,440.00
inventory 500mg
10-20 days ฿112,500.00

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(6R,7R)-3-(Chloromethyl)-8-oxo-7-[[2-(2-thienyl)acetyl]amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid (4-Methoxyphenyl)methyl Ester
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Used as an intermediate in the synthesis of certain cephalosporin antibiotics. The compound plays a key role in the production of semi-synthetic beta-lactam antibiotics, particularly those designed to resist degradation by bacterial enzymes. Its structure allows for modification at key positions to enhance antimicrobial activity, improve pharmacokinetics, or increase stability against beta-lactamases. Commonly employed in pharmaceutical manufacturing to develop broad-spectrum antibiotics effective agains

Used as an intermediate in the synthesis of certain cephalosporin antibiotics. The compound plays a key role in the production of semi-synthetic beta-lactam antibiotics, particularly those designed to resist degradation by bacterial enzymes. Its structure allows for modification at key positions to enhance antimicrobial activity, improve pharmacokinetics, or increase stability against beta-lactamases. Commonly employed in pharmaceutical manufacturing to develop broad-spectrum antibiotics effective against both gram-positive and gram-negative bacteria.

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