Cas 778647-45-3,2-pyridin-2-yl-quinoline-4-carboxylic acid [2-(4-fluoro-3-nitro-benzoylamino)-ethyl]-amide

778647-45-3

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Basic information

Product Name: 2-pyridin-2-yl-quinoline-4-carboxylic acid [2-(4-fluoro-3-nitro-benzoylamino)-ethyl]-amide
Synonyms: 2-pyridin-2-yl-quinoline-4-carboxylic acid [2-(4-fluoro-3-nitro-benzoylamino)-ethyl]-amide
CAS NO:778647-45-3
Molecular Formula:
Molecular Weight: 459.436
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-pyridin-2-yl-quinoline-4-carboxylic acid [2-(4-fluoro-3-nitro-benzoylamino)-ethyl]-amide(CAS DataBase Reference)
NIST Chemistry Reference: 2-pyridin-2-yl-quinoline-4-carboxylic acid [2-(4-fluoro-3-nitro-benzoylamino)-ethyl]-amide(778647-45-3)
EPA Substance Registry System: 2-pyridin-2-yl-quinoline-4-carboxylic acid [2-(4-fluoro-3-nitro-benzoylamino)-ethyl]-amide(778647-45-3)

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: 778647-45-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 778647-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,8,6,4 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 778647-45:
(8*7)+(7*7)+(6*8)+(5*6)+(4*4)+(3*7)+(2*4)+(1*5)=233
233 % 10 = 3
So 778647-45-3 is a valid CAS Registry Number.

778647-45-3Upstream product

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778647-45-3Relevant academic research and scientific papers

Preparation and evaluation of bipyridyl-tagged reagents and scavengers

Convers, Emmanuelle,Tye, Heather,Whittaker, Mark

, p. 8729 - 8738 (2007/10/03)

The synthesis of three bipyridyl-tagged reagents and one scavenger is described. Of the three reagents, the carbodiimide derivative proved to be effective as a coupling reagent for amide formation and the removal of the coupling side product from the reac

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