Cas 913530-57-1,2-(4-chlorophenyl)sulfonylmethyl-6-(4-fluorophenyl)-3-nitroimidazo[1,2-a]pyridine

913530-57-1

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Basic information

Product Name: 2-(4-chlorophenyl)sulfonylmethyl-6-(4-fluorophenyl)-3-nitroimidazo[1,2-a]pyridine
Synonyms: 2-(4-chlorophenyl)sulfonylmethyl-6-(4-fluorophenyl)-3-nitroimidazo[1,2-a]pyridine
CAS NO:913530-57-1
Molecular Formula:
Molecular Weight: 445.858
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: 2-(4-chlorophenyl)sulfonylmethyl-6-(4-fluorophenyl)-3-nitroimidazo[1,2-a]pyridine(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-chlorophenyl)sulfonylmethyl-6-(4-fluorophenyl)-3-nitroimidazo[1,2-a]pyridine(913530-57-1)
EPA Substance Registry System: 2-(4-chlorophenyl)sulfonylmethyl-6-(4-fluorophenyl)-3-nitroimidazo[1,2-a]pyridine(913530-57-1)

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: 913530-57-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 913530-57-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,5,3 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 913530-57:
(8*9)+(7*1)+(6*3)+(5*5)+(4*3)+(3*0)+(2*5)+(1*7)=151
151 % 10 = 1
So 913530-57-1 is a valid CAS Registry Number.

913530-57-1Upstream product

913530-57-1Downstream Products

913530-64-0 diethyl 2-[6-(4-fluorophenyl)-3-nitroimidazo[1,2-a]pyridin-2-ylmethylene]malonate

913530-57-1Relevant academic research and scientific papers

Efficient synthesis of new 8-aryl tricyclic pyridinones

Castera-Ducros, Caroline,Crozet, Maxime D.,Vanelle, Patrice

, p. 2777 - 2783 (2006)

New tricyclic pyridinones were synthesized from 6-bromo-2-chloromethyl-3- nitroimidazo[1,2-a]pyridine in four steps involving a Suzuki-Miyaura cross-coupling reaction and a direct olefination with diethyl ketomalonate as key steps. Subsequent one-pot redu

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