Cas 958747-63-2,8-[(4-methylbenzene)sulfonyl]-13-oxa-8,10-diazatetracyclo-[7.7.0.02,7.011,15]hexadeca-1<sup>(9)</sup>,2<sup>(7)</sup>,3,5,10,15-hexaen-12-one

958747-63-2

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Basic information

Product Name: 8-[(4-methylbenzene)sulfonyl]-13-oxa-8,10-diazatetracyclo-[7.7.0.02,7.011,15]hexadeca-1⁽⁹⁾,2⁽⁷⁾,3,5,10,15-hexaen-12-one
Synonyms:
CAS NO:958747-63-2
Molecular Formula:
Molecular Weight: 378.408
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: 8-[(4-methylbenzene)sulfonyl]-13-oxa-8,10-diazatetracyclo-[7.7.0.02,7.011,15]hexadeca-1⁽⁹⁾,2⁽⁷⁾,3,5,10,15-hexaen-12-one(CAS DataBase Reference)
NIST Chemistry Reference: 8-[(4-methylbenzene)sulfonyl]-13-oxa-8,10-diazatetracyclo-[7.7.0.02,7.011,15]hexadeca-1⁽⁹⁾,2⁽⁷⁾,3,5,10,15-hexaen-12-one(958747-63-2)
EPA Substance Registry System: 8-[(4-methylbenzene)sulfonyl]-13-oxa-8,10-diazatetracyclo-[7.7.0.02,7.011,15]hexadeca-1⁽⁹⁾,2⁽⁷⁾,3,5,10,15-hexaen-12-one(958747-63-2)

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: 958747-63-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 958747-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,7,4 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 958747-63:
(8*9)+(7*5)+(6*8)+(5*7)+(4*4)+(3*7)+(2*6)+(1*3)=242
242 % 10 = 2
So 958747-63-2 is a valid CAS Registry Number.

958747-63-2Upstream product

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958747-63-2Relevant 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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