Cas 1060718-05-9,(Z)-2-(6-methoxy-3-nitropyridin-2-yl)-3-(5-phenylthiophen-2-yl)acrylonitrile

1060718-05-9

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Basic information

Product Name: (Z)-2-(6-methoxy-3-nitropyridin-2-yl)-3-(5-phenylthiophen-2-yl)acrylonitrile
Synonyms: (Z)-2-(6-methoxy-3-nitropyridin-2-yl)-3-(5-phenylthiophen-2-yl)acrylonitrile
CAS NO:1060718-05-9
Molecular Formula:
Molecular Weight: 363.397
EINECS: N/A
Product Categories: N/A
Mol File: 1060718-05-9.mol
Article Data: 1

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: (Z)-2-(6-methoxy-3-nitropyridin-2-yl)-3-(5-phenylthiophen-2-yl)acrylonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-(6-methoxy-3-nitropyridin-2-yl)-3-(5-phenylthiophen-2-yl)acrylonitrile(1060718-05-9)
EPA Substance Registry System: (Z)-2-(6-methoxy-3-nitropyridin-2-yl)-3-(5-phenylthiophen-2-yl)acrylonitrile(1060718-05-9)

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: 1060718-05-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1060718-05-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,0,7,1 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1060718-05:
(9*1)+(8*0)+(7*6)+(6*0)+(5*7)+(4*1)+(3*8)+(2*0)+(1*5)=119
119 % 10 = 9
So 1060718-05-9 is a valid CAS Registry Number.

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1060718-05-9Relevant articles and documents

Synthesis of C3-substituted 4-azaindoles: An easy access to 4-azamelatonin and protected 4-azatryptophan

Jeanty, Matthieu,Suzenet, Franck,Guillaumet, Gerald

supporting information; experimental part, p. 7390 - 7393 (2009/05/07)

(Chemical Equation Presented) C3-Substituted-4-azaindoles were synthesized from pyridylacetonitriles in a two-step sequence allowing the easy introduction of a range of substituents. This strategy permits the rapid synthesis of 4-azamelatonin and a protec

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