Cas 1394236-91-9,13-methyl-8-[(4-methylbenzene)sulfonyl]8,10,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1(16),2(7),3,5,9,11(15)-hexaen-12-one

1394236-91-9

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Basic information

Product Name: 13-methyl-8-[(4-methylbenzene)sulfonyl]8,10,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1⁽¹⁶⁾,2⁽⁷⁾,3,5,9,11⁽¹⁵⁾-hexaen-12-one
Synonyms:
CAS NO:1394236-91-9
Molecular Formula:
Molecular Weight: 391.45
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: 13-methyl-8-[(4-methylbenzene)sulfonyl]8,10,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1⁽¹⁶⁾,2⁽⁷⁾,3,5,9,11⁽¹⁵⁾-hexaen-12-one(CAS DataBase Reference)
NIST Chemistry Reference: 13-methyl-8-[(4-methylbenzene)sulfonyl]8,10,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1⁽¹⁶⁾,2⁽⁷⁾,3,5,9,11⁽¹⁵⁾-hexaen-12-one(1394236-91-9)
EPA Substance Registry System: 13-methyl-8-[(4-methylbenzene)sulfonyl]8,10,13-triazatetracyclo[7.7.0.02,7.011,15]hexadeca-1⁽¹⁶⁾,2⁽⁷⁾,3,5,9,11⁽¹⁵⁾-hexaen-12-one(1394236-91-9)

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: 1394236-91-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1394236-91-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,2,3 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1394236-91:
(9*1)+(8*3)+(7*9)+(6*4)+(5*2)+(4*3)+(3*6)+(2*9)+(1*1)=179
179 % 10 = 9
So 1394236-91-9 is a valid CAS Registry Number.

1394236-91-9Upstream product

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1394236-91-9Relevant academic research and scientific papers

An intramolecular inverse electron demand Diels-Alder approach to annulated α-carbolines

Ma, Zhiyuan,Ni, Feng,Woo, Grace H. C.,Lo, Sie-Mun,Roveto, Philip M.,Schaus, Scott E.,Snyder, John K.

, p. 829 - 840 (2012/07/17)

Intramolecular inverse electron demand cycloadditions of isatin-derived 1,2,4-triazines with acetylenic dienophiles tethered by amidations or transesterifications proceed in excellent yields to produce lactam- or lactone-fused α-carbolines. Beginning with various isatins and alkynyl dienophiles, a pilot-scale library of eighty-eight α-carbolines was prepared by using this robust methodology for biological evaluation.

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