Cas 1541206-75-0,(E)-3-(3-allyl-2-selenoxo-2,3-dihydro-1H-imidazol-1-yl)-3-phenyl-2-propenenitrile

1541206-75-0

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Basic information

Product Name: (E)-3-(3-allyl-2-selenoxo-2,3-dihydro-1H-imidazol-1-yl)-3-phenyl-2-propenenitrile
Synonyms: (E)-3-(3-allyl-2-selenoxo-2,3-dihydro-1H-imidazol-1-yl)-3-phenyl-2-propenenitrile
CAS NO:1541206-75-0
Molecular Formula:
Molecular Weight: 314.248
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: (E)-3-(3-allyl-2-selenoxo-2,3-dihydro-1H-imidazol-1-yl)-3-phenyl-2-propenenitrile(CAS DataBase Reference)
NIST Chemistry Reference: (E)-3-(3-allyl-2-selenoxo-2,3-dihydro-1H-imidazol-1-yl)-3-phenyl-2-propenenitrile(1541206-75-0)
EPA Substance Registry System: (E)-3-(3-allyl-2-selenoxo-2,3-dihydro-1H-imidazol-1-yl)-3-phenyl-2-propenenitrile(1541206-75-0)

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: 1541206-75-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1541206-75-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,4,1,2,0 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1541206-75:
(9*1)+(8*5)+(7*4)+(6*1)+(5*2)+(4*0)+(3*6)+(2*7)+(1*5)=130
130 % 10 = 0
So 1541206-75-0 is a valid CAS Registry Number.

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1541206-75-0Relevant academic research and scientific papers

Three-component reaction of imidazoles, cyanophenylacetylene, and chalcogens: Stereoselective synthesis of 3-alkenyl-2-imidazolethiones and -selones

Belyaeva, Kseniya V.,Andriyankova, Ludmila V.,Nikitina, Lina P.,Mal'Kina, Anastasiya G.,Afonin, Andrei V.,Ushakov, Igor A.,Bagryanskaya, Irina Yu.,Trofimov, Boris A.

, p. 1091 - 1098 (2014/01/23)

The three-component reaction of 1-substituted imidazoles, cyanophenylacetylene, and elemental sulfur or selenium proceeds readily (for sulfur at room temperature without solvent, and for selenium in boiling MeCN) to stereoselectively afford 3-(Z)-cyanophe

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