Cas 1373264-06-2,N-(3-(3,4-dihydronaphthalen-1(2H)-ylidene)-2-methylallyl)-4-methylbenzenesulfonamide

1373264-06-2

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Basic information

Product Name: N-(3-(3,4-dihydronaphthalen-1(2H)-ylidene)-2-methylallyl)-4-methylbenzenesulfonamide
Synonyms: N-(3-(3,4-dihydronaphthalen-1(2H)-ylidene)-2-methylallyl)-4-methylbenzenesulfonamide
CAS NO:1373264-06-2
Molecular Formula:
Molecular Weight: 353.485
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-(3-(3,4-dihydronaphthalen-1(2H)-ylidene)-2-methylallyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(3-(3,4-dihydronaphthalen-1(2H)-ylidene)-2-methylallyl)-4-methylbenzenesulfonamide(1373264-06-2)
EPA Substance Registry System: N-(3-(3,4-dihydronaphthalen-1(2H)-ylidene)-2-methylallyl)-4-methylbenzenesulfonamide(1373264-06-2)

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: 1373264-06-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1373264-06-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,2,6 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1373264-06:
(9*1)+(8*3)+(7*7)+(6*3)+(5*2)+(4*6)+(3*4)+(2*0)+(1*6)=152
152 % 10 = 2
So 1373264-06-2 is a valid CAS Registry Number.

1373264-06-2Upstream product

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1373264-06-2Relevant academic research and scientific papers

Coinage metals-catalyzed cascade reactions of aryl alkynylaziridines: Silver(I)-single vs gold(I)-double cyclizations

Kern, Nicolas,Blanc, Aurelien,Miaskiewicz, Solene,Robinette, Michelle,Weibel, Jean-Marc,Pale, Patrick

, p. 4323 - 4341 (2012/06/18)

Alkynylaziridines carrying an aryl group could be efficiently converted into aminoallenylidene isochromans, isoquinolines, or tetrahydronaphtalenes with silver(I) salts and into 1-azaspiro[4.5]decane derivatives with gold(I) complexes. Mechanistic investi

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