76577-82-7 Usage
Uses
Used in Pharmaceutical Industry:
Pyrrolo[1,2-a]quinoline-2-carboxylic acid ethyl ester is used as a building block for the synthesis of various biologically active molecules and pharmaceutical compounds. Its unique structure and properties contribute to the development of new drugs with potential applications in treating a range of diseases.
Used in Medicinal Chemistry Research:
Pyrrolo[1,2-a]quinoline-2-carboxylic acid ethyl ester is used as a research tool for investigating its pharmacological properties, including anti-cancer and anti-inflammatory activities. This helps in understanding its potential as a therapeutic agent and in the design of novel drug candidates.
Used in Organic Synthesis:
Pyrrolo[1,2-a]quinoline-2-carboxylic acid ethyl ester is used as a key intermediate in the synthesis of complex organic molecules. Its versatile structure allows for the formation of a variety of derivatives, making it a valuable component in the creation of new chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 76577-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,7 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76577-82:
(7*7)+(6*6)+(5*5)+(4*7)+(3*7)+(2*8)+(1*2)=177
177 % 10 = 7
So 76577-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H13NO2/c1-2-18-15(17)12-9-13-8-7-11-5-3-4-6-14(11)16(13)10-12/h3-10H,2H2,1H3
76577-82-7Relevant academic research and scientific papers
A mild preparation of substituted indolizines and indole from simple aromatic precursors using (trimethylsilyl)diazomethane
Zhu, Liusheng,Vimolratana, Marc,Brown, Sean P.,Medina, Julio C.
, p. 1768 - 1770 (2008/09/18)
A mild and convenient synthesis of substituted indolizines from readily available 2-(pyridin-2-yl)acetyl derivatives using (trimethylsilyl)diazomethane is described. The extension of this methodology to the synthesis of indole from 2-aminobenzaldehyde is also reported.
Synthesis and oral antiallergic activity of carboxylic acids derived from imidazo[2,1-c][1,4]benzoxazines, imidazo[1,2-a]quinolines, imidazo[1,2-a]quinoxalines, imidazo[1,2-a]quinoxalinones, pyrrolo[1,2-a]quinoxalinones, pyrrolo[2,3-a]quinoxalinones, and
Ager,Barnes,Danswan,Hairsine,Kay,Kennewell,Matharu,Miller,Robson,Rowlands,Tully,Westwood
, p. 1098 - 1115 (2007/10/02)
4H-Imidazo[2,1-c][1,4]benzoxazine-1-carboxylic acid (3) was found to possess potent activity in the IgE-induced rat passive cutaneous anaphylaxis model which may be predictive of clinical antiallergic activity. Compared to disodium cromoglycate (DSCG,1),
