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  • DC Chemicals Limited
  • China
  • Product Name: Nitrocefin
  • Price: $Inquiry/100mg $Inquiry/250mg $Inquiry/500mg
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

41906-86-9

41906-86-9 structure
41906-86-9 structure
  • Name: nitrocefin
  • Chemical Name: nitrocefin
  • CAS Number: 41906-86-9
  • Molecular Formula: C21H16N4O8S2
  • Molecular Weight: 516.504
  • Create Date: 2018-09-20 16:48:45
  • Modify Date: 2024-01-02 23:01:20
  • Nitrocefin is a chromogenic β-lactamase substrate that undergoes distinctive color change from yellow to red as the amide bond in the β-lactam ring is hydrolyzed by β-lactamase. Nitrocefin is used in competitive inhibition studies in developmental work on β-lactamase-resistant antibiotics[1].

Name nitrocefin
Synonyms (6R-(3(E),6a,7b))-3-(2-(2,4-Dinitrophenyl)ethenyl)-8-oxo-7-((2-thienylacetyl)amino)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[(E)-2-(2,4-dinitrophenyl)ethenyl]-8-oxo-7-[[2-(2-thienyl)acetyl]amino]-, (6R,7R)-
nitrocefin
(6R,7R)-3-[(E)-2-(2,4-Dinitrophenyl)vinyl]-8-oxo-7-[(2-thienylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Description Nitrocefin is a chromogenic β-lactamase substrate that undergoes distinctive color change from yellow to red as the amide bond in the β-lactam ring is hydrolyzed by β-lactamase. Nitrocefin is used in competitive inhibition studies in developmental work on β-lactamase-resistant antibiotics[1].
Related Catalog
References

[1]. Shannon K, Phillips I. beta-Lactamase detection by three simple methods: Intralactam, nitrocefin and acidimetric. J Antimicrob Chemother. 1980 Sep;6(5):617-21.

Density 1.7±0.1 g/cm3
Boiling Point 872.0±65.0 °C at 760 mmHg
Melting Point >99℃
Molecular Formula C21H16N4O8S2
Molecular Weight 516.504
Flash Point 481.2±34.3 °C
Exact Mass 516.040955
PSA 231.89000
LogP 1.04
Vapour Pressure 0.0±0.3 mmHg at 25°C
Index of Refraction 1.749

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41906-86-9 structure

41906-86-9

Literature: Lee, Mijoon; Hesek, Dusan; Mobashery, Shahriar Journal of Organic Chemistry, 2005 , vol. 70, # 1 p. 367 - 369

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41906-86-9 structure

41906-86-9

Literature: Lee, Mijoon; Hesek, Dusan; Mobashery, Shahriar Journal of Organic Chemistry, 2005 , vol. 70, # 1 p. 367 - 369
Precursor  1

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