139896-91-6 Usage
General Description
2-Quinolinecarboxylic acid, 4-bromo-, Methyl ester 97% is a chemical compound with a high purity level of 97%. It is a methyl ester derivative of 4-bromo-2-quinolinecarboxylic acid, which is commonly used in organic synthesis and pharmaceutical research. 2-Quinolinecarboxylic acid, 4-broMo-, Methyl ester 97% has various applications in the pharmaceutical industry, such as in the development of new drugs and medicines. Its high purity level makes it suitable for use in sensitive analytical techniques and reactions requiring high-quality reagents. Overall, 2-Quinolinecarboxylic acid, 4-bromo-, Methyl ester 97% is a valuable chemical compound with important applications in the field of pharmaceuticals and organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 139896-91-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,8,9 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 139896-91:
(8*1)+(7*3)+(6*9)+(5*8)+(4*9)+(3*6)+(2*9)+(1*1)=196
196 % 10 = 6
So 139896-91-6 is a valid CAS Registry Number.
139896-91-6Relevant articles and documents
COMPOUNDS FOR THE INHIBITION OF CELLULAR PROLIFERATION
-
, (2012/02/01)
Compositions and methods for inhibiting translation are provided. Compositions, methods and kits for treating (1) cellular proliferative disorders, (2) non-proliferative, degenerative disorders, (3) viral infections, (4) disorders associated with viral infections, and/or (5) non-proliferative metabolic disorders such as type II diabetes where inhibition of translation initiation is beneficial using the compounds disclosed herein.
3-(2-Carboxyindol-3-yl)propionic Acid-Based Antagonists of the N-Methyl-D-aspartic Acid Receptor Associated Glycine Binding Site
Salituro, Francesco G.,Harrison, Boyd L.,Baron, Bruce M.,Nyce, Philip L.,Stewart, Kenneth T.,et al.
, p. 1791 - 1799 (2007/10/02)
A series of substituted 3-(2-carboxyindol-3-yl)propionic acids was synthesized and tested as antagonists for the strychnine-insensitive glycine binding site of the NMDA receptor.Chlorine, and other small electron-withdrawing substituents in the 4- and 6-p
