Cas no 2231676-70-1 (2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one)

2,2,2-Trifluoro-1-(1H-indazol-4-yl)ethan-1-one is a fluorinated ketone derivative featuring an indazole moiety, which imparts unique reactivity and structural versatility. The trifluoromethyl group enhances electrophilicity, making it a valuable intermediate in organic synthesis, particularly for the construction of heterocyclic compounds and fluorinated pharmaceuticals. Its indazole core is significant in medicinal chemistry due to its bioisosteric properties and potential pharmacological activity. The compound’s high purity and stability under standard conditions ensure reliable performance in coupling reactions, nucleophilic substitutions, and other transformations. Its well-defined structure facilitates precise modifications, making it a preferred choice for research in drug discovery and agrochemical development.
2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one structure
2231676-70-1 structure
Product Name:2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one
CAS No:2231676-70-1
MF:C9H5F3N2O
MW:214.144012212753
MDL:MFCD31621157
CID:5303615
Update Time:2025-06-08

2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one Chemical and Physical Properties

Names and Identifiers

    • 2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one
    • MDL: MFCD31621157
    • Inchi: 1S/C9H5F3N2O/c10-9(11,12)8(15)5-2-1-3-7-6(5)4-13-14-7/h1-4H,(H,13,14)
    • InChI Key: DWJNDFAWMIMDFP-UHFFFAOYSA-N
    • SMILES: C(C1=CC=CC2=C1C=NN2)(=O)C(F)(F)F

2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Advanced ChemBlocks
P43641-1G
2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one
2231676-70-1 95%
1G
$1,465 2023-09-15

Additional information on 2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one

Introduction to 2,2,2-Trifluoro-1-(1H-Indazol-4-yl)ethan-1-one (CAS No. 2231676-70-1)

2,2,2-Trifluoro-1-(1H-indazol-4-yl)ethan-1-one, with the CAS number 2231676-70-1, is a synthetic compound that has garnered significant attention in the fields of medicinal chemistry and pharmaceutical research. This compound is characterized by its unique molecular structure, which includes a trifluoromethyl group and an indazole ring. These structural features contribute to its potential biological activities and make it a valuable candidate for various therapeutic applications.

The chemical formula of 2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one is C10H6F3N3O, and its molecular weight is approximately 237.16 g/mol. The compound is a white crystalline solid at room temperature and is soluble in common organic solvents such as dimethyl sulfoxide (DMSO) and dimethylformamide (DMF). Its physical and chemical properties have been extensively studied to understand its behavior in different environments and its potential for pharmaceutical development.

In recent years, 2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one has been the subject of numerous research studies due to its promising pharmacological properties. One of the key areas of interest is its potential as an inhibitor of specific enzymes involved in various disease pathways. For instance, studies have shown that this compound can effectively inhibit the activity of certain kinases, which are crucial enzymes in cell signaling pathways. This inhibition can lead to the modulation of cellular processes such as proliferation, apoptosis, and migration, making it a potential candidate for the treatment of cancers and other proliferative disorders.

Beyond its enzymatic inhibition properties, 2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one has also been investigated for its anti-inflammatory effects. Inflammation is a complex biological response to harmful stimuli and is a key factor in many chronic diseases. Research has demonstrated that this compound can reduce the production of pro-inflammatory cytokines and chemokines, thereby mitigating inflammatory responses. This property makes it a promising candidate for the development of anti-inflammatory drugs.

The pharmacokinetic profile of 2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one has also been studied to evaluate its suitability for therapeutic use. Preclinical studies have shown that it exhibits good oral bioavailability and a favorable distribution profile. Additionally, it has demonstrated low toxicity in animal models, which is a crucial factor for its potential use in human clinical trials. These findings suggest that 2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one has a favorable safety profile and may be suitable for further development as a therapeutic agent.

In the context of drug discovery and development, the ability to synthesize compounds with specific structural features is crucial. The synthesis of 2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one involves several steps that require precise control over reaction conditions to ensure high yields and purity. Recent advancements in synthetic chemistry have led to more efficient and scalable methods for producing this compound. These improvements have facilitated its availability for research purposes and have paved the way for further exploration of its biological activities.

Clinical trials are an essential step in the drug development process to assess the safety and efficacy of new compounds. While clinical trials involving 2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one are still in their early stages, preliminary results are promising. Phase I trials have shown that the compound is well-tolerated by patients at various dose levels and has demonstrated preliminary evidence of therapeutic activity. These findings warrant further investigation in larger-scale clinical trials to fully evaluate its potential as a therapeutic agent.

In conclusion, 2,2,2-trifluoro-1-(1H-indazol-4-yl)ethan-1-one (CAS No. 2231676-70-1) is a promising compound with diverse biological activities that make it a valuable candidate for pharmaceutical research and development. Its unique molecular structure confers specific pharmacological properties that have been validated through extensive preclinical studies. Ongoing research continues to explore its potential applications in treating various diseases, particularly those involving inflammation and cancer. As more data from clinical trials become available, the therapeutic potential of this compound will become clearer.

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