ChemicalBook--->CAS DataBase List--->101182-25-6

101182-25-6

101182-25-6 Structure

101182-25-6 Structure
IdentificationBack Directory
[Name]

(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
[CAS]

101182-25-6
[Synonyms]

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
(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
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-(chloromethyl)-8-oxo-7-[[2-(2-thienyl)acetyl]amino]-, (4-methoxyphenyl)methyl ester, (6R,7R)-
[Molecular Formula]

C22H21ClN2O5S2
[MOL File]

101182-25-6.mol
[Molecular Weight]

493
Chemical PropertiesBack Directory
[Boiling point ]

764.6±60.0 °C(Predicted)
[density ]

1.47±0.1 g/cm3(Predicted)
[solubility ]

Dichloromethane
[form ]

Solid
[pka]

12.98±0.60(Predicted)
[color ]

Off White
Hazard InformationBack Directory
[Uses]

(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 is an intermediate in synthesizing Nitrocefin (N493815), a chromogenic β-lactamase substrate that undergoes colour change from yellow to red as the amide bond in the β-Lactam ring is hydrolyzed by β-lactamase. Nitrocefin undergoes colour changes induced by lactamases produced by Gram-positive and Gram-negative bacteria. Several studies have utilized the colour changing properties of Nitrocefin for the detection of β-lactamase activity from bacterial cell extracts by isoelectric focusing and spectroscopy. Nitrocefin has also been used in studies involving β-lactamase resistant antibiotics.
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