Description

(alphaR)-4-Chloro-2-(3-methyl-1H-pyrazol-1-yl)-alpha-(trifluoromethyl)benzenemethanol (CAS: 1033805-26-3) is a high-purity chiral organic compound with the molecular formula C₁₂H₁₀ClF₃N₂O. This compound features a trifluoromethyl group and a pyrazole moiety, making it a valuable intermediate in pharmaceutical and agrochemical research. Its IUPAC name is (1R)-1-[4-chloro-2-(3-methylpyrazol-1-yl)phenyl]-2,2,2-trifluoroethanol, and it is characterized by its stereospecific (R)-configuration. Suitable for use in asymmetric synthesis, catalysis, and medicinal chemistry applications, this product is rigorously tested for quality, ensuring optimal performance in demanding research environments. Available in various quantities with detailed analytical data (HPLC, NMR, MS) provided.

Properties

• CAS Number: 1033805-26-3
• Complexity: 316
• IUPAC Name: (1R)-1-[4-chloro-2-(3-methylpyrazol-1-yl)phenyl]-2,2,2-trifluoro-ethanol
• InChI: InChI=1S/C12H10ClF3N2O/c1-7-4-5-18(17-7)10-6-8(13)2-3-9(10)11(19)12(14,15)16/h2-6,11,19H,1H3/t11-/m1/s1
• InChI Key: YBMVIGVXVXAKDM-LLVKDONJSA-N
• Exact Mass: 290.0433751
• Molecular Formula: C12H10ClF3N2O
• Molecular Weight: 290.67
• SMILES: CC1=NN(C=C1)C2=C(C=CC(=C2)Cl)[C@H](C(F)(F)F)O
• Topological: 38.1
• Monoisotopic Mass: 290.0433751
• Synonyms: 1033805-26-3, DTXSID901139415, (R)-1-[4-chloro-2-(3-methylpyrazol-1-yl)phenyl]-2,2,2-trifluoroethanol, (R)-1-(4-Chloro-2-(3-methylpyrazol-1-yl)phenyl)-2,2,2-trifluoroethanol, DTXCID301571037, (alphaR)-4-Chloro-2-(3-methyl-1H-pyrazol-1-yl)-alpha-(trifluoromethyl)benzenemethanol, 812-407-8, (R)-1-(4-chloro-2-(3-methyl-1H-pyrazol-1-yl)phenyl)-2,2,2-trifluoroethanol, (1R)-1-[4-chloro-2-(3-methyl-1H-pyrazol-1-yl)phenyl]-2,2,2-trifluoroethan-1-ol, (R)-1-(4-chloro-2-(3-methyl-1H-pyrazol-1-yl)phenyl)-2,2,2-trifluoroethan-1-ol, (1R)-1-[4-chloro-2-(3-methylpyrazol-1-yl)phenyl]-2,2,2-trifluoroethanol, MFCD23099027, SCHEMBL613559, BCP15953, CS-M3311, AKOS027336642, AC-31307, AS-49441, DB-102362, I10362, (I+/-R)-4-Chloro-2-(3-methyl-1H-pyrazol-1-yl)-I+/–(trifluoromethyl)benzenemethanol

Application

This compound serves as a key chiral building block in the synthesis of biologically active molecules, particularly in the development of pharmaceuticals and agrochemicals. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug discovery. Researchers utilize it in asymmetric catalysis and as a precursor for novel therapeutic agents targeting CNS and inflammatory diseases.

Safety and Hazards

GHS Hazard Statements

• Not Classified
• Reported as not meeting GHS hazard criteria by 1 of 1 companies. For more detailed information, please visit ECHA C&L website.

Hazard Classes and Categories

• Not Classified

If you are interested or have any questions, please contact us at support@atomfair.com

Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.