1236127-55-1 Usage
Uses
Used in Pharmaceutical Research:
6-Methoxy-1-Methyl-1H-indazole is used as a research compound for exploring its potential therapeutic properties. Its unique chemical structure allows scientists to study its interactions with biological systems and evaluate its efficacy in treating various diseases.
Used in Drug Development:
In the pharmaceutical industry, 6-Methoxy-1-Methyl-1H-indazole is used as a lead compound in drug development. Its chemical properties and potential therapeutic effects make it a promising candidate for the creation of new medications to address unmet medical needs.
Used in Chemical Synthesis:
6-Methoxy-1-Methyl-1H-indazole is also used as a building block in the synthesis of other organic compounds. Its versatile structure can be modified to create a variety of new molecules with different properties and applications in various fields, including materials science and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 1236127-55-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,6,1,2 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1236127-55:
(9*1)+(8*2)+(7*3)+(6*6)+(5*1)+(4*2)+(3*7)+(2*5)+(1*5)=131
131 % 10 = 1
So 1236127-55-1 is a valid CAS Registry Number.
1236127-55-1Relevant articles and documents
A general, one-step synthesis of substituted indazoles using a flow reactor
Wheeler, Rob C.,Baxter, Emma,Campbell, Ian B.,MacDonald, Simon J. F.
, p. 565 - 569 (2011)
Flow chemistry is a rapidly emerging technology within the pharmaceutical industry, both within medicinal and development chemistry groups. The advantages of flow chemistry, increased safety, improved reproducibility, enhanced scalability, are readily apparent, and we aimed to exploit this technology in order to provide small amounts of pharmaceutically interesting fragments via a safe and scalable route, which would enable the rapid synthesis of multigram quantities on demand. Here we report a general and versatile route which utilises flow chemistry to deliver a range of known and novel indazoles, including 3-amino and 3-hydroxy analogues.
