Cas 1456599-44-2,2-(4-fluorophenyl)-3,3-bis((3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)thio)acrylonitrile

1456599-44-2

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Basic information

Product Name: 2-(4-fluorophenyl)-3,3-bis((3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)thio)acrylonitrile
Synonyms: 2-(4-fluorophenyl)-3,3-bis((3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)thio)acrylonitrile
CAS NO:1456599-44-2
Molecular Formula:
Molecular Weight: 903.466
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-fluorophenyl)-3,3-bis((3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)thio)acrylonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-fluorophenyl)-3,3-bis((3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)thio)acrylonitrile(1456599-44-2)
EPA Substance Registry System: 2-(4-fluorophenyl)-3,3-bis((3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)thio)acrylonitrile(1456599-44-2)

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: 1456599-44-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1456599-44-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,6,5,9 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1456599-44:
(9*1)+(8*4)+(7*5)+(6*6)+(5*5)+(4*9)+(3*9)+(2*4)+(1*4)=212
212 % 10 = 2
So 1456599-44-2 is a valid CAS Registry Number.

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1456599-44-2Relevant academic research and scientific papers

An electrogenerated base-promoted synthesis of 2-Aryl-3,3- Bis((Perfluoroalkyl) Thio)acrylonitriles

Saied, Taieb,Raouafi, Noureddine,Boujlel, Khaled

, p. 1320 - 1326 (2013/10/08)

The preparation of 2-aryl-3,3-bis((perfluoroalkyl)thio)acrylonitriles is described. The electrogenerated cyanomethyl base/anion obtained from electroreduction of acetonitrile promotes reactions between arylacetonitrile, carbon disulfide, and perfluoroalky

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