Cas 1309568-70-4,2,2'-[2,2'-(piperazine-1,4-diyl)bis(4-phenylthiazole-5,2-diyl)]diethene-1,1,2-tricarbonitrile

1309568-70-4

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Basic information

Product Name: 2,2'-[2,2'-(piperazine-1,4-diyl)bis(4-phenylthiazole-5,2-diyl)]diethene-1,1,2-tricarbonitrile
Synonyms: 2,2'-[2,2'-(piperazine-1,4-diyl)bis(4-phenylthiazole-5,2-diyl)]diethene-1,1,2-tricarbonitrile
CAS NO:1309568-70-4
Molecular Formula:
Molecular Weight: 606.694
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: 2,2'-[2,2'-(piperazine-1,4-diyl)bis(4-phenylthiazole-5,2-diyl)]diethene-1,1,2-tricarbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2,2'-[2,2'-(piperazine-1,4-diyl)bis(4-phenylthiazole-5,2-diyl)]diethene-1,1,2-tricarbonitrile(1309568-70-4)
EPA Substance Registry System: 2,2'-[2,2'-(piperazine-1,4-diyl)bis(4-phenylthiazole-5,2-diyl)]diethene-1,1,2-tricarbonitrile(1309568-70-4)

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: 1309568-70-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1309568-70-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,5,6 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1309568-70:
(9*1)+(8*3)+(7*0)+(6*9)+(5*5)+(4*6)+(3*8)+(2*7)+(1*0)=174
174 % 10 = 4
So 1309568-70-4 is a valid CAS Registry Number.

1309568-70-4Upstream product

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1309568-70-4Relevant academic research and scientific papers

An improved method for tricyanovinilation of aromatic amines under ultrasound irradiation

Deligeorgiev, Todor,Lesev, Nedyalko,Kaloyanova, Stefka

experimental part, p. 74 - 78 (2012/01/05)

A synthetic method for tricyanovinylation under ultrasound irradiation has been developed for preparation of tricyanovinyl aromatic amines. The method is reliable and can be applied to the synthesis of a variety of tricyanovinyl compounds, with high yields, purity and with short reaction times.

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