Cas 1357149-23-5,2-[4-(1H-indol-2-yl)phenoxy]-N-[4-(N-thiazol-2-ylsulfamoyl)phenyl]acetamide

1357149-23-5

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Basic information

Product Name: 2-[4-(1H-indol-2-yl)phenoxy]-N-[4-(N-thiazol-2-ylsulfamoyl)phenyl]acetamide
Synonyms: 2-[4-(1H-indol-2-yl)phenoxy]-N-[4-(N-thiazol-2-ylsulfamoyl)phenyl]acetamide
CAS NO:1357149-23-5
Molecular Formula:
Molecular Weight: 504.59
EINECS: N/A
Product Categories: N/A
Mol File: 1357149-23-5.mol
Article Data: 1

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: 2-[4-(1H-indol-2-yl)phenoxy]-N-[4-(N-thiazol-2-ylsulfamoyl)phenyl]acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-[4-(1H-indol-2-yl)phenoxy]-N-[4-(N-thiazol-2-ylsulfamoyl)phenyl]acetamide(1357149-23-5)
EPA Substance Registry System: 2-[4-(1H-indol-2-yl)phenoxy]-N-[4-(N-thiazol-2-ylsulfamoyl)phenyl]acetamide(1357149-23-5)

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: 1357149-23-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1357149-23-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,1,4 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1357149-23:
(9*1)+(8*3)+(7*5)+(6*7)+(5*1)+(4*4)+(3*9)+(2*2)+(1*3)=165
165 % 10 = 5
So 1357149-23-5 is a valid CAS Registry Number.

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1357149-23-5Relevant articles and documents

Synthesis, molecular docking study and antitumor activity of novel 2-phenylindole derivatives

El-Nakkady, Sally S.,Hanna, Mona M.,Roaiah, Hanaa M.,Ghannam, Iman A.Y.

experimental part, p. 387 - 398 (2012/03/09)

The starting material, 4-(1-indol-2-yl)phenol 1 was obtained via Fischer synthesis. Vilsmeir Haack's formylation of 1 gave the carboxaldehyde derivative 2 which was subjected to different reactions affording the 3-substituted compounds 3-10. Co

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