66751-33-5 Usage
Uses
Used in Pharmaceutical Industry:
6-Hydroxy-5-azaindoline serves as a key building block for the development of various biologically active compounds and pharmaceuticals. Its unique structure and properties make it a valuable component in the creation of new drugs and therapeutic agents.
Used in Cancer Therapy:
6-Hydroxy-5-azaindoline is utilized in cancer therapy research due to its potential antioxidant and anti-inflammatory properties. These characteristics may contribute to the development of novel treatments for various types of cancer, offering new hope for patients and healthcare professionals.
Used in Neurodegenerative Disease Research:
6-hydroxy-5-azaindoline's potential antioxidant and anti-inflammatory properties also make it a candidate for research into neurodegenerative diseases. Its ability to combat oxidative stress and inflammation may lead to the development of new treatments for conditions such as Alzheimer's, Parkinson's, and multiple sclerosis.
Used in Organic Synthesis:
6-Hydroxy-5-azaindoline is employed in the synthesis of organic compounds and materials, where its unique structure and reactivity can be leveraged to create new molecules with specific properties and applications.
Overall, 6-hydroxy-5-azaindoline's diverse potential applications across various industries highlight its importance as a compound of interest for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 66751-33-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,7,5 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66751-33:
(7*6)+(6*6)+(5*7)+(4*5)+(3*1)+(2*3)+(1*3)=145
145 % 10 = 5
So 66751-33-5 is a valid CAS Registry Number.
66751-33-5Relevant academic research and scientific papers
AZAINDOLINE DERIVATIVES: 62.* SYNTHESIS AND TRANSFORMATIONS OF CONDENSED THREE-RING SYSTEMS THAT INCLUDE A 5-AZAINDOLINE FRAGMENT
Azimov, V. A.,Bychikhina, N. N.,Yakhontov, L. N.
, p. 1061 - 1064 (2007/10/02)
The reaction of 7-carbamoyl and 7-cyano-6-chloro-5-azaindolines with hydrazine leads to the formation of pyrrolopyrazolopyridine, whereas the reaction of 7-carbamoyl-5-azaindolines with dimethylformamide diethylacetal gives pyrrolopyr
