Cas 1198790-79-2,4-methyl-N-(3-oxo-3-phenyl-1-(3,4,5-trimethoxyphenyl)propyl)benzenesulfonamide

1198790-79-2

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Basic information

Product Name: 4-methyl-N-(3-oxo-3-phenyl-1-(3,4,5-trimethoxyphenyl)propyl)benzenesulfonamide
Synonyms: 4-methyl-N-(3-oxo-3-phenyl-1-(3,4,5-trimethoxyphenyl)propyl)benzenesulfonamide
CAS NO:1198790-79-2
Molecular Formula:
Molecular Weight: 469.558
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: 4-methyl-N-(3-oxo-3-phenyl-1-(3,4,5-trimethoxyphenyl)propyl)benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-methyl-N-(3-oxo-3-phenyl-1-(3,4,5-trimethoxyphenyl)propyl)benzenesulfonamide(1198790-79-2)
EPA Substance Registry System: 4-methyl-N-(3-oxo-3-phenyl-1-(3,4,5-trimethoxyphenyl)propyl)benzenesulfonamide(1198790-79-2)

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: 1198790-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1198790-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,7,9 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1198790-79:
(9*1)+(8*1)+(7*9)+(6*8)+(5*7)+(4*9)+(3*0)+(2*7)+(1*9)=222
222 % 10 = 2
So 1198790-79-2 is a valid CAS Registry Number.

1198790-79-2Upstream product

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1198790-79-2Relevant academic research and scientific papers

Simple and efficient access to N-tosyl β-amino ketones and their conversion into 2,4-disubstituted azetidines

Das, Biswanath,Balasubramanyam, Penagaluri,Veeranjaneyulu, Boyapati,Reddy, Gandolla Chinna

supporting information; experimental part, p. 9505 - 9508 (2010/03/04)

(Chemical Equation Presented) Treatment of N-tosylaldimines with acetophenone at room temperature in the presence of BF3· OEt2 as a catalyst furnished the corresponding N-tosyl β-amino ketones in high yields (77-86%) within 6-9 h. Su

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