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Δ2-Cefepime

Product Name
Δ2-Cefepime
CAS No.
88040-25-9
Chemical Name
Δ2-Cefepime
Synonyms
Δ2-Cefepime;Δ2-Cefepime;Δ2-CefepiMe Etherate;Cefepime Δ - 3 Isomer;Cefepime Δ - 3 Isomer;Δ2-CefepiMe Etherate Dihydrochloride Salt;1-[[(6R,7R)-7-[[(2Z)-2-(2-AMino-4-thiazolyl)-2-(MethoxyiMino)acetyl]aMino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-3-en-3-yl]Methyl]-1-MethylpyrrolidiniuM Inner Salt Etherate;(6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(1-methylpyrrolidin-1-ium-1-yl)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylate,ethoxyethane
CBNumber
CB02508627
Molecular Formula
C23H34N6O6S2
Formula Weight
554.68266
MOL File
88040-25-9.mol
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Δ2-Cefepime Property

Melting point:
>151°C (dec.)
storage temp. 
Amber Vial, -20°C Freezer, Under Inert Atmosphere
solubility 
Water (Slightly)
form 
Solid
color 
White to Off-White
InChIKey
DBCVQAGQPYVVDA-XVKMNWMGSA-N
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
C242743
Product name
Δ2-Cefepime
Packaging
2.5mg
Price
$120
Updated
2021/12/16
AK Scientific
Product number
7513DU
Product name
(6R,7R)-7-[[(2Z)-2-(2-Amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(1-methylpyrrolidin-1-ium-1-yl)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylate;ethoxyethane
Packaging
1mg
Price
$211
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC19856
Product name
Delta2-Cefepime etherate
Packaging
2mg
Price
$218.1
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC19856
Product name
Delta2-Cefepime etherate
Packaging
5mg
Price
$396.4
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC19856
Product name
Delta2-Cefepime etherate
Packaging
10mg
Price
$720.8
Updated
2021/12/16
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Δ2-Cefepime Chemical Properties,Usage,Production

Uses

Δ2-Cefepime is the Δ2-isomer of Cefepime (C242750), a new series of cephalosporins.

Uses

The Δ2-isomer of Cefepime (C242750), a new series of cephalosporins.

Preparation

First, cefepime and N-trimethylsilylacetamide were added to dichloromethane for 0.5 h. Subsequently, triethylamine dissolved in dichloromethane was added to the reaction system between 2-5 °C. Adjust the temperature to 2-5 °C and react for 24 h. After adding water, the aqueous layer was separated, and the aqueous phase was washed with methylene chloride. Wait for the solution to cool to 2-5 °C and adjust the pH=3 with sulfuric acid. Stir the resulting slurry for 2h. Filter to collect the solids and wash with water, adjust the pH=7.5-8.0 with sodium bicarbonate aqueous solution, add carbon, and stir for 30 min. Filter the mixture to collect the filtrate and adjust pH=3 with sulfuric acid. Finally, the solids are filtered and collected, and product Δ2-Cefepime is obtained by washing and drying.

Δ2-Cefepime Preparation Products And Raw materials

Raw materials

Preparation Products

88040-25-9, Δ2-CefepimeRelated Search:


  • Δ2-Cefepime
  • Δ2-CefepiMe Etherate
  • (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-[(1-methylpyrrolidin-1-ium-1-yl)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylate,ethoxyethane
  • 1-[[(6R,7R)-7-[[(2Z)-2-(2-AMino-4-thiazolyl)-2-(MethoxyiMino)acetyl]aMino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-3-en-3-yl]Methyl]-1-MethylpyrrolidiniuM Inner Salt Etherate
  • Δ2-CefepiMe Etherate Dihydrochloride Salt
  • Cefepime Δ - 3 Isomer
  • Δ2-Cefepime
  • Cefepime Δ - 3 Isomer
  • 88040-25-9
  • C23H34N6O6S2
  • Chiral Reagents
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Sulfur & Selenium Compounds