Cas 1312772-82-9,N-(7-chloro-quinolin-4-yl)-N'-[4-(6-p-tolyl[1,2,4,5]tetroxan-3-yl)benzylidene]ethane-1,2-diamine

1312772-82-9

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Basic information

Product Name: N-(7-chloro-quinolin-4-yl)-N'-[4-(6-p-tolyl[1,2,4,5]tetroxan-3-yl)benzylidene]ethane-1,2-diamine
Synonyms: N-(7-chloro-quinolin-4-yl)-N'-[4-(6-p-tolyl[1,2,4,5]tetroxan-3-yl)benzylidene]ethane-1,2-diamine
CAS NO:1312772-82-9
Molecular Formula:
Molecular Weight: 489.958
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: N-(7-chloro-quinolin-4-yl)-N'-[4-(6-p-tolyl[1,2,4,5]tetroxan-3-yl)benzylidene]ethane-1,2-diamine(CAS DataBase Reference)
NIST Chemistry Reference: N-(7-chloro-quinolin-4-yl)-N'-[4-(6-p-tolyl[1,2,4,5]tetroxan-3-yl)benzylidene]ethane-1,2-diamine(1312772-82-9)
EPA Substance Registry System: N-(7-chloro-quinolin-4-yl)-N'-[4-(6-p-tolyl[1,2,4,5]tetroxan-3-yl)benzylidene]ethane-1,2-diamine(1312772-82-9)

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: 1312772-82-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1312772-82-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,7,7 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1312772-82:
(9*1)+(8*3)+(7*1)+(6*2)+(5*7)+(4*7)+(3*2)+(2*8)+(1*2)=139
139 % 10 = 9
So 1312772-82-9 is a valid CAS Registry Number.

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1312772-82-9Relevant academic research and scientific papers

Synthesis and in vitro antimalarial activity of tetraoxane-amine/amide conjugates

Kumar, Nitin,Khan, Shabana I.,Atheaya, Himanshu,Mamgain, Ritu,Rawat, Diwan S.

, p. 2816 - 2827 (2011/07/08)

A series of tetraoxanes, tetraoxane-amine and tetraoxane-amide conjugates have been synthesized and screened for in vitro antimalarial activity against chloroquine-sensitive and chloroquine-resistant strains of Plasmodium falciparum. Most of the conjugate

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