Cas 1291079-87-2,N-(2-(1-hydroxy-1-phenyl-3-(m-tolyl)prop-2-ynyl)phenyl)-4-methylbenzenesulfonamide

1291079-87-2

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Basic information

Product Name: N-(2-(1-hydroxy-1-phenyl-3-(m-tolyl)prop-2-ynyl)phenyl)-4-methylbenzenesulfonamide
Synonyms: N-(2-(1-hydroxy-1-phenyl-3-(m-tolyl)prop-2-ynyl)phenyl)-4-methylbenzenesulfonamide
CAS NO:1291079-87-2
Molecular Formula:
Molecular Weight: 467.588
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-(2-(1-hydroxy-1-phenyl-3-(m-tolyl)prop-2-ynyl)phenyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(2-(1-hydroxy-1-phenyl-3-(m-tolyl)prop-2-ynyl)phenyl)-4-methylbenzenesulfonamide(1291079-87-2)
EPA Substance Registry System: N-(2-(1-hydroxy-1-phenyl-3-(m-tolyl)prop-2-ynyl)phenyl)-4-methylbenzenesulfonamide(1291079-87-2)

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: 1291079-87-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1291079-87-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,1,0,7 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1291079-87:
(9*1)+(8*2)+(7*9)+(6*1)+(5*0)+(4*7)+(3*9)+(2*8)+(1*7)=172
172 % 10 = 2
So 1291079-87-2 is a valid CAS Registry Number.

1291079-87-2Upstream product

1291079-87-2Downstream Products

1291080-01-7 3-iodo-4-phenyl-2-(m-tolyl)quinoline

1291079-87-2Relevant academic research and scientific papers

Electrophile-driven regioselective synthesis of functionalized quinolines

Ali, Shaukat,Zhu, Hai-Tao,Xia, Xiao-Feng,Ji, Ke-Gong,Yang, Yan-Fang,Song, Xian-Rong,Liang, Yong-Min

, p. 2598 - 2601 (2011/06/26)

Highly substituted 3-iodoquinolines bearing different alkyl and aryl moieties can be synthesized in moderate to excellent yields (up to 99%) by 6-endo-dig iodocyclization of 2-tosylaminophenylprop-1-yn-3-ols with molecular iodine (I2) under mil

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