The chemical substance with the name "(S)-3-(4,6-bis(((R)-1,1,1-trifluoropropan-2-yl)amino)-1,3,5-triazin-2-yl)-2,6,6-trifluorocyclohex-2-en-1-ol" and CAS number "2301974-60-5" is characterized by its complex molecular structure, which includes a triazine ring and a cyclohexene derivative. The presence of multiple trifluoromethyl groups contributes to its unique chemical properties, such as increased lipophilicity and potential biological activity. The stereochemistry indicated by the (S) and (R) designations suggests that the compound exhibits chirality, which can influence its interaction with biological systems, potentially affecting its pharmacological profile. The compound may exhibit properties such as stability under various conditions, solubility in organic solvents, and specific reactivity patterns due to the functional groups present. Its potential applications could span across fields such as pharmaceuticals, agrochemicals, or materials science, depending on its biological activity and chemical behavior. Further studies would be necessary to elucidate its specific characteristics and potential uses in various applications.

(S)-3-(4,6-bis(((R)-1,1,1-trifluoropropan-2-yl)amino)- 1,3,5-triazin-2-yl)-2,6,6-trifluorocyclohex-2-en-1-ol

2301974-60-5: The chemical substance with the name "(S)-3-(4,6-bis(((R)-1,1,1-trifluoropropan-2-yl)amino)-1,3,5-triazin-2-yl)-2,6,6-trifluorocyclohex-2-en-1-ol" and CAS number "2301974-60-5" is characterized by its complex molecular structure, which includes a triazine ring and a cyclohexene derivative. The presence of multiple trifluoromethyl groups contributes to its unique chemical properties, such as increased lipophilicity and potential biological activity. The stereochemistry indicated by the (S) and (R) designations suggests that the compound exhibits chirality, which can influence its interaction with biological systems, potentially affecting its pharmacological profile. The compound may exhibit properties such as stability under various conditions, solubility in organic solvents, and specific reactivity patterns due to the functional groups present. Its potential applications could span across fields such as pharmaceuticals, agrochemicals, or materials science, depending on its biological activity and chemical behavior. Further studies would be necessary to elucidate its specific characteristics and potential uses in various applications.

<p>Ranolisib is an isocitrate dehydrogenase (IDH) inhibitor known for its antitumor activity.</p>

CAS 2301974-60-5

(S)-3-(4,6-bis(((R)-1,1,1-trifluoropropan-2-yl)amino)- 1,3,5-triazin-2-yl)-2,6,6-trifluorocyclohex-2-en-1-ol

Ranosidenib

Ref: TM-T201237