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Phenol, 3-[1-(tetrahydro-2H-pyran-2-yl)-5-[1-(triphenylmethyl)-1H-1,2,4-triazol-3-yl]-1H-indazol-3-yl]is a complex organic compound characterized by the presence of phenol, tetrahydro-2H-pyran-2-yl, triphenylmethyl, and 1H-indazol-3-yl functional groups. Phenol,
3-[1-(tetrahydro-2H-pyran-2-yl)-5-[1-(triphenylmethyl)-1H-1,2,4-triazol-3-
yl]-1H-indazol-3-yl]features a combination of aromatic rings and heterocyclic structures, which may endow it with unique properties such as biological activity or solubility in various solvents. Its potential applications in medicinal chemistry, drug discovery, and organic synthesis warrant further research and exploration.

395104-16-2

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395104-16-2 Usage

Uses

Used in Medicinal Chemistry:
Phenol, 3-[1-(tetrahydro-2H-pyran-2-yl)-5-[1-(triphenylmethyl)-1H-1,2,4-triazol-3-yl]-1H-indazol-3-yl]is used as a building block or intermediate in the synthesis of pharmaceutical compounds due to its diverse functional groups and structural features. Its unique properties may contribute to the development of novel drugs with improved efficacy and selectivity.
Used in Drug Discovery:
Phenol,
3-[1-(tetrahydro-2H-pyran-2-yl)-5-[1-(triphenylmethyl)-1H-1,2,4-triazol-3-
yl]-1H-indazol-3-yl]is utilized in drug discovery processes to identify potential lead candidates for the treatment of various diseases. Its complex structure and multiple functional groups may offer new opportunities for the design of innovative therapeutic agents with enhanced pharmacological properties.
Used in Organic Synthesis:
Phenol, 3-[1-(tetrahydro-2H-pyran-2-yl)-5-[1-(triphenylmethyl)-1H-1,2,4-triazol-3-yl]-1H-indazol-3-yl]serves as a versatile starting material or reagent in organic synthesis, enabling the preparation of a wide range of chemical products. Its unique structural features and functional groups can be exploited to synthesize complex organic molecules with potential applications in various industries.
Used in Chemical Research:
Phenol,
3-[1-(tetrahydro-2H-pyran-2-yl)-5-[1-(triphenylmethyl)-1H-1,2,4-triazol-3-
yl]-1H-indazol-3-yl]is employed in chemical research to study the properties and reactivity of its functional groups and structural elements. Understanding its behavior in various chemical reactions can provide valuable insights into the development of new synthetic methods and the discovery of novel chemical entities.

Check Digit Verification of cas no

The CAS Registry Mumber 395104-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,5,1,0 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 395104-16:
(8*3)+(7*9)+(6*5)+(5*1)+(4*0)+(3*4)+(2*1)+(1*6)=142
142 % 10 = 2
So 395104-16-2 is a valid CAS Registry Number.

395104-16-2Upstream product

395104-16-2Relevant academic research and scientific papers

Solid forms of a JNK inhibitor

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Page/Page column 17, (2010/11/24)

The present invention provides solid forms of Compound (I), pharmaceutical compositions thereof, and methods for the treatment or prevention of diseases including, but not limited to a liver disease, cancer, a cardiovascular disease, a metabolic disease, a renal disease, an autoimmune condition, an inflammatory condition, macular degeneration, pain and related syndromes, disease-related wasting, an asbestos-related condition, pulmonary hypertension, ischemia/reperfusion injury, central nervous system (CNS) injury/damage or a disease treatable or preventable by the inhibition of JNK. In particular, the invention relates to certain novel crystal forms of the compound 1-(5-(1H-1,2,4-triazol-5-yl)(1H-indazol-3-yl))-3-(2-piperidylethoxy)benzene.

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