(6R,7R)-7-Amino-3-(methoxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

98%

Reagent Code: #231019
label
Alias Cefopoxime ester parent nucleus, 7-amino-3-methoxymethyl-3-cefene-4-carboxylic acid
fingerprint
CAS Number 24701-69-7

science Other reagents with same CAS 24701-69-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.27 g/mol
Formula C₉H₁₂N₂O₄S
badge Registry Numbers
MDL Number MFCD09839433
thermostat Physical Properties
Boiling Point 511.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of cephalosporin antibiotics, particularly second-generation cephalosporins like cefoxitin. It plays a key role in developing antimicrobial agents effective against a broad spectrum of bacteria, including gram-positive, gram-negative, and anaerobic bacteria, as well as those resistant to other antibiotics. Its beta-lactam core structure allows for chemical modifications that enhance antibiotic stability, potency, and resistance to beta-lactamase enzymes. Widely utilized in pharmaceutical manufacturing for producing injectable antibiotic formulations.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿760.00
5g
10-20 days ฿2,740.00
25g
10-20 days ฿9,660.00
100g
10-20 days ฿37,540.00
(6R,7R)-7-Amino-3-(methoxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
No image available

Used as an intermediate in the synthesis of cephalosporin antibiotics, particularly second-generation cephalosporins like cefoxitin. It plays a key role in developing antimicrobial agents effective against a broad spectrum of bacteria, including gram-positive, gram-negative, and anaerobic bacteria, as well as those resistant to other antibiotics. Its beta-lactam core structure allows for chemical modifications that enhance antibiotic stability, potency, and resistance to beta-lactamase enzymes. Widely ut

Used as an intermediate in the synthesis of cephalosporin antibiotics, particularly second-generation cephalosporins like cefoxitin. It plays a key role in developing antimicrobial agents effective against a broad spectrum of bacteria, including gram-positive, gram-negative, and anaerobic bacteria, as well as those resistant to other antibiotics. Its beta-lactam core structure allows for chemical modifications that enhance antibiotic stability, potency, and resistance to beta-lactamase enzymes. Widely utilized in pharmaceutical manufacturing for producing injectable antibiotic formulations.

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...