Cas 1218989-08-2,N-(2-(8-hydroxyquinolin-2-yl)-1-phenylethyl)-4-methylbenzenesulfonamide

1218989-08-2

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Basic information

Product Name: N-(2-(8-hydroxyquinolin-2-yl)-1-phenylethyl)-4-methylbenzenesulfonamide
Synonyms: N-(2-(8-hydroxyquinolin-2-yl)-1-phenylethyl)-4-methylbenzenesulfonamide
CAS NO:1218989-08-2
Molecular Formula:
Molecular Weight: 418.516
EINECS: N/A
Product Categories: N/A
Mol File: 1218989-08-2.mol
Article Data: 2

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-(2-(8-hydroxyquinolin-2-yl)-1-phenylethyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2-(8-hydroxyquinolin-2-yl)-1-phenylethyl)-4-methylbenzenesulfonamide(1218989-08-2)
EPA Substance Registry System: N-(2-(8-hydroxyquinolin-2-yl)-1-phenylethyl)-4-methylbenzenesulfonamide(1218989-08-2)

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: 1218989-08-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1218989-08-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,8,9,8 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1218989-08:
(9*1)+(8*2)+(7*1)+(6*8)+(5*9)+(4*8)+(3*9)+(2*0)+(1*8)=192
192 % 10 = 2
So 1218989-08-2 is a valid CAS Registry Number.

1218989-08-2Upstream product

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1218989-08-2Relevant articles and documents

3-Component synthesis of α-substituted sulfonamides via Br?nsted acid-catalyzed C(sp3)-H bond functionalization of 2-alkylazaarenes

Beisel,Kirchner,Kaehler,Knauer,Soltani,Manolikakes

supporting information, p. 5525 - 5528 (2016/07/06)

A Br?nsted acid-catalyzed addition of 2-alkylazaarenes to in situ generated N-sulfonylimines through selective C(sp3)-H bond functionalization has been developed. This protocol provides an atom- and step-economic approach to α-substituted sulfo

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