(6R,7R)-4-Methoxybenzyl 3-(chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate

97%

Reagent Code: #230140
fingerprint
CAS Number 104146-10-3

science Other reagents with same CAS 104146-10-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 486.97 g/mol
Formula C₂₄H₂₃ClN₂O₅S
thermostat Physical Properties
Melting Point 153-155°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of cephalosporin antibiotics. It plays a key role in the production of semi-synthetic beta-lactam antibiotics, particularly those requiring specific side chain modifications for enhanced antimicrobial activity. Its structure allows for further chemical modifications to improve stability, bioavailability, and resistance to beta-lactamase enzymes. Commonly employed in pharmaceutical manufacturing to develop broad-spectrum antibiotics effective against both Gram-positive and Gram-negative bacteria.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿290.00
25g
10-20 days ฿384.00
100g
10-20 days ฿1,850.00
500g
10-20 days ฿8,880.00
(6R,7R)-4-Methoxybenzyl 3-(chloromethyl)-8-oxo-7-(2-phenylacetamido)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
No image available

Used as an intermediate in the synthesis of cephalosporin antibiotics. It plays a key role in the production of semi-synthetic beta-lactam antibiotics, particularly those requiring specific side chain modifications for enhanced antimicrobial activity. Its structure allows for further chemical modifications to improve stability, bioavailability, and resistance to beta-lactamase enzymes. Commonly employed in pharmaceutical manufacturing to develop broad-spectrum antibiotics effective against both Gram-posi

Used as an intermediate in the synthesis of cephalosporin antibiotics. It plays a key role in the production of semi-synthetic beta-lactam antibiotics, particularly those requiring specific side chain modifications for enhanced antimicrobial activity. Its structure allows for further chemical modifications to improve stability, bioavailability, and resistance to beta-lactamase enzymes. Commonly employed in pharmaceutical manufacturing to develop broad-spectrum antibiotics effective against both Gram-positive and Gram-negative bacteria.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...