Cas 1190942-97-2,4-(1-(benzo[d][1,3]dioxol-5-yl)-5-(6-methoxynaphthalen-2-yl)-3-oxopentylamino)benzene-sulfonamide

1190942-97-2

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Basic information

Product Name: 4-(1-(benzo[d][1,3]dioxol-5-yl)-5-(6-methoxynaphthalen-2-yl)-3-oxopentylamino)benzene-sulfonamide
Synonyms: 4-(1-(benzo[d][1,3]dioxol-5-yl)-5-(6-methoxynaphthalen-2-yl)-3-oxopentylamino)benzene-sulfonamide
CAS NO:1190942-97-2
Molecular Formula:
Molecular Weight: 532.617
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-(1-(benzo[d][1,3]dioxol-5-yl)-5-(6-methoxynaphthalen-2-yl)-3-oxopentylamino)benzene-sulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-(1-(benzo[d][1,3]dioxol-5-yl)-5-(6-methoxynaphthalen-2-yl)-3-oxopentylamino)benzene-sulfonamide(1190942-97-2)
EPA Substance Registry System: 4-(1-(benzo[d][1,3]dioxol-5-yl)-5-(6-methoxynaphthalen-2-yl)-3-oxopentylamino)benzene-sulfonamide(1190942-97-2)

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: 1190942-97-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1190942-97-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,0,9,4 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1190942-97:
(9*1)+(8*1)+(7*9)+(6*0)+(5*9)+(4*4)+(3*2)+(2*9)+(1*7)=172
172 % 10 = 2
So 1190942-97-2 is a valid CAS Registry Number.

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1190942-97-2Relevant academic research and scientific papers

Synthesis and antidiabetic performance of β-amino ketone containing nabumetone moiety

Wang, Hang,Yan, Ju-Fang,Song, Xiao-Li,Fan, Li,Xu, Jin,Zhou, Guang-Ming,Jiang, Li,Yang, Da-Cheng

experimental part, p. 2119 - 2130 (2012/05/05)

We wish to report the further design and improved synthesis that resulted in two series of target molecules, TM-1 and TM-2, with remarkably simplified structures containing β-amino ketone of discrete nabumetone moiety. These were obtained via a 'one-pot,

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