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1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-((1S,2S,4S,5R)-5-ethylquinuclidin-2-yl)(quinolin-4-yl)methyl)thiourea is a complex organic thiourea derivative characterized by its unique molecular structure, which includes a quinuclidine moiety and a quinoline ring. 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-((1S,2S,4S,5R)-5-ethylquinuclidin-2-yl)(quinolin-4-yl)methyl)thiourea features multiple functional groups and aromatic rings, contributing to its structural complexity. Its potential applications in medicinal chemistry, pharmacology, or other related fields are promising due to its distinctive structural features and possible biological activity. However, further research and testing are required to ascertain its specific properties and potential uses.

1362859-89-9

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1362859-89-9 Usage

Uses

Used in Medicinal Chemistry:
1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-((1S,2S,4S,5R)-5-ethylquinuclidin-2-yl)(quinolin-4-yl)methyl)thiourea is used as a compound with potential applications in medicinal chemistry for its unique structure and possible biological activity. Its complex arrangement of functional groups and aromatic rings may contribute to its interaction with biological targets, making it a candidate for the development of new drugs.
Used in Pharmacology:
In the field of pharmacology, 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-((1S,2S,4S,5R)-5-ethylquinuclidin-2-yl)(quinolin-4-yl)methyl)thiourea is used as a compound with potential for studying its interactions with various biological receptors and enzymes. Its structural complexity may allow it to modulate specific signaling pathways or target proteins, which could be beneficial in the development of therapeutic agents.
Used in Chemical Research:
1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-((1S,2S,4S,5R)-5-ethylquinuclidin-2-yl)(quinolin-4-yl)methyl)thiourea is used as a research compound for exploring its chemical properties and reactivity. Understanding how 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-((1S,2S,4S,5R)-5-ethylquinuclidin-2-yl)(quinolin-4-yl)methyl)thiourea interacts with other molecules can provide insights into new synthetic pathways or mechanisms of action that could be applied in various chemical and biological processes.
Used in Drug Design and Development:
In the pharmaceutical industry, 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-((1S,2S,4S,5R)-5-ethylquinuclidin-2-yl)(quinolin-4-yl)methyl)thiourea is used as a starting point for drug design and development. Its unique structural features may serve as a basis for the creation of new drug candidates targeting specific diseases or conditions, pending further investigation into its pharmacological properties and safety profile.

Check Digit Verification of cas no

The CAS Registry Mumber 1362859-89-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,2,8,5 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1362859-89:
(9*1)+(8*3)+(7*6)+(6*2)+(5*8)+(4*5)+(3*9)+(2*8)+(1*9)=199
199 % 10 = 9
So 1362859-89-9 is a valid CAS Registry Number.

1362859-89-9Downstream Products

1362859-89-9Relevant academic research and scientific papers

Catalytic enantioselective iodoetherification of oximes

Tripathi, Chandra Bhushan,Mukherjee, Santanu

, p. 8450 - 8453 (2013/09/02)

Organocatalysis: The first catalytic enantioselective iodoetherification of oximes is developed using commercially available N-iodosuccinimide. In the presence of a dihydrocinchonidine-derived thiourea (10 mol %), β,γ-unsaturated oximes undergo facile iodoetherification to produce Δ2-isoxazolines containing a quaternary stereogenic center generally in high yield with good to excellent enantioselectivity. Copyright

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