Cas 97100-16-8,2-Cyano-4-oxo-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-4-phenyl-butyric acid ethyl ester

97100-16-8

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Basic information

Product Name: 2-Cyano-4-oxo-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-4-phenyl-butyric acid ethyl ester
Synonyms: 2-Cyano-4-oxo-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-4-phenyl-butyric acid ethyl ester
CAS NO:97100-16-8
Molecular Formula:
Molecular Weight: 362.385
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: 2-Cyano-4-oxo-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-4-phenyl-butyric acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Cyano-4-oxo-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-4-phenyl-butyric acid ethyl ester(97100-16-8)
EPA Substance Registry System: 2-Cyano-4-oxo-3-(2-oxo-2,3-dihydro-1H-indol-3-yl)-4-phenyl-butyric acid ethyl ester(97100-16-8)

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: 97100-16-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 97100-16-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,1,0 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97100-16:
(7*9)+(6*7)+(5*1)+(4*0)+(3*0)+(2*1)+(1*6)=118
118 % 10 = 8
So 97100-16-8 is a valid CAS Registry Number.

97100-16-8Upstream product

97100-16-8Downstream Products

97100-25-9 2-Amino-4-(2-oxo-2,3-dihydro-1H-indol-3-yl)-5-phenyl-furan-3-carboxylic acid ethyl ester

97100-16-8Relevant academic research and scientific papers

Michael Reactions of 3-Acylmethyleneoxindoles with Active Methylene Compounds

Higashiyama, Kimio,Nagase, Hiromasa,Yamaguchi, Ryoji,Kawai, Ken-ichi,Otomasu, Hirotaka

, p. 544 - 550 (2007/10/02)

3-Acylmethyleneoxindoles (Ia-d) reacted with active methylene compounds (IIa-d) in EtOH, in the presence of NaOC2H5 as a catalyst at room temperature, to afford the corresponding normal Michael adducts (IIIa-f).The reactions of Ia with IIa, Ic with IIa an

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