919119-62-3 Usage
General Description
1H-Indole-2-carboxylic acid, 7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, ethyl ester is a chemical compound with potential use in medicinal chemistry and organic synthesis. It is a derivative of indole-2-carboxylic acid, which is a heterocyclic compound with various pharmaceutical and biological activities. The ethyl ester group in this compound makes it more soluble and stable, and the boron-containing group can be useful for various chemical reactions. 1H-INDOLE-2-CARBOXYLIC ACID, 7-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-, ETHYL ESTER has the potential to be used in the development of new pharmaceuticals, agrochemicals, and materials. Its specific properties and potential applications make it a valuable tool in chemical research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 919119-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,9,1,1 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 919119-62:
(8*9)+(7*1)+(6*9)+(5*1)+(4*1)+(3*9)+(2*6)+(1*2)=183
183 % 10 = 3
So 919119-62-3 is a valid CAS Registry Number.
919119-62-3Relevant articles and documents
TRANSGLUTAMINASE 2 (TG2) INHIBITORS
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Paragraph 00629, (2020/03/02)
Described herein are compounds and pharmaceutical compositions containing such compounds which inhibit transglutaminase 2 (TG2). Also described herein are methods for using such TG2 inhibitors, alone or in combination with other compounds, for treating diseases or conditions that would benefit from TG2 inhibition.
A highly selective Ir-catalyzed borylation of 2-substituted indoles: a new access to 2,7- and 2,4,7-substituted indoles
Lo, Wei Fun,Kaiser, Hanns Martin,Spannenberg, Anke,Beller, Matthias,Tse, Man Kin
, p. 371 - 375 (2007/10/03)
The selective CH-functionalization of 2-substituted indoles is presented. Using bis(pinacolato)diboron (2) in the presence of iridium complexes, a novel catalytic mono-borylation is observed preferentially at the 7-position of the indole. This allows for