Cas 1125595-64-3,ethyl 2-(5-amino-2,4-dimethoxyphenyl)-2-(1H-indol-3-yl)acetate

1125595-64-3

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Basic information

Product Name: ethyl 2-(5-amino-2,4-dimethoxyphenyl)-2-(1H-indol-3-yl)acetate
Synonyms: ethyl 2-(5-amino-2,4-dimethoxyphenyl)-2-(1H-indol-3-yl)acetate
CAS NO:1125595-64-3
Molecular Formula:
Molecular Weight: 354.406
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: ethyl 2-(5-amino-2,4-dimethoxyphenyl)-2-(1H-indol-3-yl)acetate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-(5-amino-2,4-dimethoxyphenyl)-2-(1H-indol-3-yl)acetate(1125595-64-3)
EPA Substance Registry System: ethyl 2-(5-amino-2,4-dimethoxyphenyl)-2-(1H-indol-3-yl)acetate(1125595-64-3)

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: 1125595-64-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1125595-64-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,5,5,9 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1125595-64:
(9*1)+(8*1)+(7*2)+(6*5)+(5*5)+(4*9)+(3*5)+(2*6)+(1*4)=153
153 % 10 = 3
So 1125595-64-3 is a valid CAS Registry Number.

1125595-64-3Upstream product

1125595-60-9 ethyl 2-[(2,4-dimethoxyphenyl)amino]-2-(1H-indol-3-yl)acetate

1125595-64-3Downstream Products

1125595-64-3Relevant academic research and scientific papers

News from the 80-year-old passerini variant of the Friedel-Crafts alkylation of indole

Desimoni, Giovanni,Faita, Giuseppe,Mella, Mariella,Toscanini, Marco,Boiocchi, Massimo

experimental part, p. 6232 - 6238 (2009/06/18)

The multi-component Friedel-Crafts alkylation reaction between indole (1), ethyl glyoxylate (2) and anilines (3a-f) gives, in analogy to the protocol of the old Passerini reaction, the expected ethyl 2-(arylamino)-2-(1H-indol-3-yl) acetates 4a-f. When the

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