Cas 1160211-75-5,3-{9-(4-nitrophenyl)-3,5-dioxo-4,9-diazatetracyclo[5.3.1.0<sup>2-endo,6-endo</sup>.0<sup>8-exo,10-exo</sup>]undec-4-yl}propanoic acid

1160211-75-5

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Basic information

Product Name: 3-{9-(4-nitrophenyl)-3,5-dioxo-4,9-diazatetracyclo[5.3.1.0^{2-endo,6-endo}.0^8-exo,10-exo]undec-4-yl}propanoic acid
Synonyms:
CAS NO:1160211-75-5
Molecular Formula:
Molecular Weight: 371.349
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-{9-(4-nitrophenyl)-3,5-dioxo-4,9-diazatetracyclo[5.3.1.0^{2-endo,6-endo}.0^8-exo,10-exo]undec-4-yl}propanoic acid(CAS DataBase Reference)
NIST Chemistry Reference: 3-{9-(4-nitrophenyl)-3,5-dioxo-4,9-diazatetracyclo[5.3.1.0^{2-endo,6-endo}.0^8-exo,10-exo]undec-4-yl}propanoic acid(1160211-75-5)
EPA Substance Registry System: 3-{9-(4-nitrophenyl)-3,5-dioxo-4,9-diazatetracyclo[5.3.1.0^{2-endo,6-endo}.0^8-exo,10-exo]undec-4-yl}propanoic acid(1160211-75-5)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1160211-75-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1160211-75-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,2,1 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1160211-75:
(9*1)+(8*1)+(7*6)+(6*0)+(5*2)+(4*1)+(3*1)+(2*7)+(1*5)=95
95 % 10 = 5
So 1160211-75-5 is a valid CAS Registry Number.

1160211-75-5Upstream product

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1160211-75-5Relevant academic research and scientific papers

Features of reactions between (3,5-dioxo-4-azatricyclo-[5.2.1.0 2-endo,6-endo ]dec-8-en-4-yl)carboxylic acids and p-nitrophenyl azide

Tarabara,Bondarenko,Kas'Yan

experimental part, p. 234 - 241 (2009/09/25)

Reactions were performed of (3,5-dioxo-4-azatricyclo[5.2.1.0 2-endo,6-endo ]dec-8-en-4-yl)carboxylic acids and their derivatives with p-nitrophenyl azide. A significant fact of the involvement of the carboxy group into the formation of aziridine ring was established and the intermolecular character of this process was confirmed. The structure of compounds synthesized was proved by IR and 1H NMR spectra.

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