Cas 1287189-56-3,N<sub>1</sub>,N<sub>3</sub>-bis(3,5-bis(trifluoromethyl)phenyl)-5-nitrobenzene-1,3-dicarboxamide

1287189-56-3

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Basic information

Product Name: N₁,N₃-bis(3,5-bis(trifluoromethyl)phenyl)-5-nitrobenzene-1,3-dicarboxamide
Synonyms: N₁,N₃-bis(3,5-bis(trifluoromethyl)phenyl)-5-nitrobenzene-1,3-dicarboxamide
CAS NO:1287189-56-3
Molecular Formula:
Molecular Weight: 633.35
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: N₁,N₃-bis(3,5-bis(trifluoromethyl)phenyl)-5-nitrobenzene-1,3-dicarboxamide(CAS DataBase Reference)
NIST Chemistry Reference: N₁,N₃-bis(3,5-bis(trifluoromethyl)phenyl)-5-nitrobenzene-1,3-dicarboxamide(1287189-56-3)
EPA Substance Registry System: N₁,N₃-bis(3,5-bis(trifluoromethyl)phenyl)-5-nitrobenzene-1,3-dicarboxamide(1287189-56-3)

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: 1287189-56-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1287189-56-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,7,1,8 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1287189-56:
(9*1)+(8*2)+(7*8)+(6*7)+(5*1)+(4*8)+(3*9)+(2*5)+(1*6)=203
203 % 10 = 3
So 1287189-56-3 is a valid CAS Registry Number.

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1287189-56-3Relevant academic research and scientific papers

Synthesis and NMR binding studies towards rational design of a series of electron-withdrawing diamide receptors/organocatalysts

Kinsella, Michael,Duggan, Patrick G.,Muldoon, Jimmy,Eccles, Kevin S.,Lawrence, Simon E.,Lennon, Claire M.

, p. 1125 - 1132 (2011)

A related series of bisamides have been evaluated for rational correlation between anion complexation and organocatalysis: remarkable enhancement of hydrogen bonding to anions was observed along with significant increases in catalytic activity in the Bayl

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