442910-45-4 Usage
Uses
Used in Pharmaceutical Industry:
1H-Indole-1-carboxylic acid, 7-(bromomethyl)-, 1,1-dimethylethyl ester is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique molecular structure allows for potential applications in the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
1H-Indole-1-carboxylic acid, 7-(bromomethyl)-, 1,1-dimethylethyl ester is used as a reagent in various organic synthesis processes. Its bromomethyl group and indole ring provide opportunities for further chemical reactions and modifications, making it a valuable component in the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 442910-45-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,2,9,1 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 442910-45:
(8*4)+(7*4)+(6*2)+(5*9)+(4*1)+(3*0)+(2*4)+(1*5)=134
134 % 10 = 4
So 442910-45-4 is a valid CAS Registry Number.
442910-45-4Relevant academic research and scientific papers
TRANSGLUTAMINASE 2 (TG2) INHIBITORS
-
, (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.
Substituted Indoles
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, (2017/07/14)
The invention provides for compounds of formula (I) wherein R1, R2, R3, R4, R5, and R6 have any of the values defined in the specification, and pharmaceutically acceptable salts thereof, th
Synthesis of N-protected/free indole-7-carboxaldehyde
Mohanakrishnan, Arasambattu K.,Balamurugan, Ramalingam,Ramesh, Neelamegam,Mathiselvam, Manoharan,Manavalan, Subramaniam
, p. 4343 - 4352 (2008/03/13)
A direct method for the preparation of N-protected/free indole-7-carboxaldehyde is reported from the corresponding N-protected 7-bromomethylindoles using three different conditions. Copyright Taylor & Francis Group, LLC.
