Cas 1602923-10-3,N-(5-hydroxy-5-(3-methyl-2-(methylsulfonamido)phenyl)pent-3-yn-1-yl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide

1602923-10-3

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Basic information

Product Name: N-(5-hydroxy-5-(3-methyl-2-(methylsulfonamido)phenyl)pent-3-yn-1-yl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide
Synonyms: N-(5-hydroxy-5-(3-methyl-2-(methylsulfonamido)phenyl)pent-3-yn-1-yl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide
CAS NO:1602923-10-3
Molecular Formula:
Molecular Weight: 556.704
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-(5-hydroxy-5-(3-methyl-2-(methylsulfonamido)phenyl)pent-3-yn-1-yl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(5-hydroxy-5-(3-methyl-2-(methylsulfonamido)phenyl)pent-3-yn-1-yl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide(1602923-10-3)
EPA Substance Registry System: N-(5-hydroxy-5-(3-methyl-2-(methylsulfonamido)phenyl)pent-3-yn-1-yl)-N-(4-methoxybenzyl)-4-methylbenzenesulfonamide(1602923-10-3)

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: 1602923-10-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1602923-10-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,2,9,2 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1602923-10:
(9*1)+(8*6)+(7*0)+(6*2)+(5*9)+(4*2)+(3*3)+(2*1)+(1*0)=133
133 % 10 = 3
So 1602923-10-3 is a valid CAS Registry Number.

1602923-10-3Upstream product

1602923-10-3Downstream Products

1602922-63-3 4a-(4-methoxyphenyl)-6-methyl-5-(methylsulfonyl)-2-tosyl-1,2,3,4,4a,5-hexahydrobenzo[b][1,6]naphthyridine

1602923-10-3Relevant academic research and scientific papers

Construction of divergent fused heterocycles via an acid-promoted intramolecular ipso-Friedel-Crafts alkylation of phenol derivatives

Yokosaka, Takuya,Shiga, Naoki,Nemoto, Tetsuhiro,Hamada, Yasumasa

, p. 3866 - 3875 (2014/05/20)

Two different cascade cyclization processes were developed using aryl group-substituted propargyl alcohol derivatives with a p-hydroxybenzylamine unit as common substrates. Using TFA as an acid promoter, an intramolecular ipso-Friedel-Crafts alkylation of

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