Cas 95411-89-5,2H-Indol-2-one, 1,3-dihydro-3-[3-[(4-methoxyphenyl)amino]-2-methyl-2-propenylidene]-1 -methyl-

95411-89-5

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Basic information

Product Name: 2H-Indol-2-one, 1,3-dihydro-3-[3-[(4-methoxyphenyl)amino]-2-methyl-2-propenylidene]-1 -methyl-
Synonyms:
CAS NO:95411-89-5
Molecular Formula: C20H20N2O2
Molecular Weight: 320.391
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: 2H-Indol-2-one, 1,3-dihydro-3-[3-[(4-methoxyphenyl)amino]-2-methyl-2-propenylidene]-1 -methyl-(CAS DataBase Reference)
NIST Chemistry Reference: 2H-Indol-2-one, 1,3-dihydro-3-[3-[(4-methoxyphenyl)amino]-2-methyl-2-propenylidene]-1 -methyl-(95411-89-5)
EPA Substance Registry System: 2H-Indol-2-one, 1,3-dihydro-3-[3-[(4-methoxyphenyl)amino]-2-methyl-2-propenylidene]-1 -methyl-(95411-89-5)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
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RTECS:
HazardClass: N/A
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Hazardous Substances Data: 95411-89-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95411-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,4,1 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 95411-89:
(7*9)+(6*5)+(5*4)+(4*1)+(3*1)+(2*8)+(1*9)=145
145 % 10 = 5
So 95411-89-5 is a valid CAS Registry Number.

95411-89-5Upstream product

90563-58-9 1-methyl-1H-indol-2-ol

95411-89-5Downstream Products

95411-89-5Relevant academic research and scientific papers

RING-CHAIN TAUTOMERISM OF VINYLOGS OF 2(3)-AMINO DERIVATIVES OF HETEROCYCLIC o-HYDROXY ALDEHYDES

Dubonosov, A. D.,Sitkina, L. M.,Bren', V. A.,Bushkov, A. Ya.,Minkin, V. I.

, p. 951 - 957 (2007/10/02)

Previously unknown vinylogs of 2(3)-aminomethylene-substituted benzothiophene-3-one, 1-methyloxindole, 1-methylindoxyl, benzofuran-3-one, and indan-1,3-dione have been synthesized.Their tautomeric transformations have been studied by methods of UV, IR, and PMR spectroscopy.It has been shown that the introduction of a substituent into the β position of a dienic chain favors the appearance of the cyclic form.

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