Cas 112419-22-4,DL-(1α,2β,4β,5β,7β,8α)-3-(4-Methylphenylsulfonyl)-6-oxa-3,9,10-triazatetracyclo<6.3.0.0<sup>2,4</sup>.0<sup>5,7</sup>>undec-9-en

112419-22-4

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Basic information

Product Name: DL-(1α,2β,4β,5β,7β,8α)-3-(4-Methylphenylsulfonyl)-6-oxa-3,9,10-triazatetracyclo<6.3.0.0^2,4.0^5,7>undec-9-en
Synonyms:
CAS NO:112419-22-4
Molecular Formula:
Molecular Weight: 305.357
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: DL-(1α,2β,4β,5β,7β,8α)-3-(4-Methylphenylsulfonyl)-6-oxa-3,9,10-triazatetracyclo<6.3.0.0^2,4.0^5,7>undec-9-en(CAS DataBase Reference)
NIST Chemistry Reference: DL-(1α,2β,4β,5β,7β,8α)-3-(4-Methylphenylsulfonyl)-6-oxa-3,9,10-triazatetracyclo<6.3.0.0^2,4.0^5,7>undec-9-en(112419-22-4)
EPA Substance Registry System: DL-(1α,2β,4β,5β,7β,8α)-3-(4-Methylphenylsulfonyl)-6-oxa-3,9,10-triazatetracyclo<6.3.0.0^2,4.0^5,7>undec-9-en(112419-22-4)

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: 112419-22-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112419-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,1 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112419-22:
(8*1)+(7*1)+(6*2)+(5*4)+(4*1)+(3*9)+(2*2)+(1*2)=84
84 % 10 = 4
So 112419-22-4 is a valid CAS Registry Number.

112419-22-4Upstream product

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112419-22-4Relevant academic research and scientific papers

cis-/trans--O,N,C-Tris-?-homobenzenes - Syntheses, ?2+?2+?2>Cycloreversions, O,N-Heteronines

Zipperer, Bernhard,Mueller, Klaus-Helmut,Gallenkamp, Bernd,Hildebrand, Rainer,Fletschinger, Michael,et al.

, p. 757 - 780 (2007/10/02)

For the cis-O,O,N-tris-?-homobenzenes 1a,b three alternative syntheses, ultimately starting from benzene or p-quinone, have been devised.In the course of one of these approaches the radical bromination of (tosylimino)-1,4-cyclohexadiene and the equilibrat

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