906000-39-3 Usage
Description
3-iodo-1H-indazole-6-carbonitrile is a heterocyclic chemical compound characterized by the molecular formula C8H4IN3. It features a five-membered ring with three nitrogen atoms and one iodine atom, along with a carbonitrile functional group, which is a carbon atom triple-bonded to a nitrogen atom. This unique structure and potential reactivity make it a compound of interest in organic synthesis and medicinal chemistry. Its possible biological activity also suggests its utility in the development of pharmaceutical drugs or agrochemicals, positioning it as a versatile chemical with applications across various scientific and industrial domains.
Uses
Used in Organic Synthesis:
3-iodo-1H-indazole-6-carbonitrile is used as a synthetic intermediate for the preparation of various organic compounds due to its unique structure and reactivity. Its presence in reactions can lead to the formation of new compounds with potential applications in different industries.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-iodo-1H-indazole-6-carbonitrile is utilized as a building block for the design and synthesis of new pharmaceutical agents. Its structural features may contribute to the development of drugs with novel mechanisms of action or improved pharmacological properties.
Used in Pharmaceutical Drug Development:
3-iodo-1H-indazole-6-carbonitrile is employed as a key component in the creation of potential pharmaceutical drugs. Its biological activity and chemical properties make it a candidate for further research and development, aiming to discover new therapeutic agents for various medical conditions.
Used in Agrochemical Development:
In agrochemicals, 3-iodo-1H-indazole-6-carbonitrile may be used as a precursor or active ingredient in the development of new pesticides, herbicides, or other crop protection products. Its unique chemical structure could offer new modes of action or enhanced efficacy in agricultural applications.
Overall, 3-iodo-1H-indazole-6-carbonitrile is a complex and promising chemical with a wide range of potential applications across various industries, including organic synthesis, medicinal chemistry, pharmaceuticals, and agrochemicals. Its unique structure and potential reactivity make it a valuable compound for further exploration and development.
Check Digit Verification of cas no
The CAS Registry Mumber 906000-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,0,0 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 906000-39:
(8*9)+(7*0)+(6*6)+(5*0)+(4*0)+(3*0)+(2*3)+(1*9)=123
123 % 10 = 3
So 906000-39-3 is a valid CAS Registry Number.
906000-39-3Relevant articles and documents
ALKYNYL ALCOHOLS AND METHODS OF USE
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, (2015/03/13)
The invention relates to compounds of Formula (0): wherein Q, A1-A8, R4 and R5 and each has the meaning as described herein. Compounds of Formula (0) and pharmaceutical compositions thereof are useful in the treatment of diseases and disorders in which undesired or over- activation of NF-kB signaling is observed.
