1-(3-(Trifluoromethyl)benzyl)-1H-pyrazole-4-carboxylic acid

Base Information

• Chemical Name: 1-(3-(Trifluoromethyl)benzyl)-1H-pyrazole-4-carboxylic acid
• CAS No.: 752222-88-1
• Molecular Formula: C12H9F3N2O2
• Molecular Weight: 270.211
• Hs Code.: 2933199090
• European Community (EC) Number: 921-977-8
• DSSTox Substance ID: DTXSID00467533
• Wikidata: Q82294511
• Mol file: 752222-88-1.mol

Synonyms:752222-88-1;1-(3-(Trifluoromethyl)benzyl)-1H-pyrazole-4-carboxylic acid;1-[[3-(trifluoromethyl)phenyl]methyl]pyrazole-4-carboxylic Acid;1-{[3-(Trifluoromethyl)phenyl]methyl}-1H-pyrazole-4-carboxylic acid;1-(3-Trifluoromethyl-benzyl)-1H-pyrazole-4-carboxylic acid;1-(3-(Trifluoromethyl)benzyl)-1H-pyrazole-4-carboxylicacid;1-(3-Trifluoromethylbenzyl)-1H-pyrazole-4-carboxylic acid;1-[3-(Trifluoromethyl)benzyl]-1H-pyrazole-4-carboxylic acid;1-{[3-(trifluoromethyl)phenyl]methyl}pyrazole-4-carboxylic acid;SCHEMBL243561;DTXSID00467533;CFB22288;MFCD09965729;AKOS009585311;AB92430;KS-6925;CS-0052663;P18725;1-{[3-(trifluoromethyl)phenyl]methyl}pyrazol-4-carboxylic acid;1-{[3-(trifluoromethyl)phenyl]methyl} pyrazole-4-carboxylic acid;1-{[3-(TRIFLUOROMETHYL)PHENYL]METHYL-1H-PYRAZOLE-4-CARBOXYLIC ACID

Chemical Property of 1-(3-(Trifluoromethyl)benzyl)-1H-pyrazole-4-carboxylic acid

Chemical Property:

• PSA: 55.12000
• LogP: 2.64840
• XLogP3: 2.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 270.06161202
• Heavy Atom Count: 19
• Complexity: 335

Purity/Quality:

97% ^*data from raw suppliers

1-(3-Trifluoromethyl-benzyl)-1H-pyrazole-4-carboxylicacid 95%+ ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC(=C1)C(F)(F)F)CN2C=C(C=N2)C(=O)O

Technology Process of 1-(3-(Trifluoromethyl)benzyl)-1H-pyrazole-4-carboxylic acid

There total 3 articles about 1-(3-(Trifluoromethyl)benzyl)-1H-pyrazole-4-carboxylic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

ethyl 1-{[3-(trifluoromethyl)phenyl]methyl}-1H-pyrazole-4-carboxylate (1035224-53-3) → 1-(3-(trifluoromethyl)benzyl)-1H-pyrazole-4-carboxylic acid (752222-88-1)

Guidance literature:

With potassium hydroxide; In methanol; for 18h; Heating;

DOI:10.1021/jm051268+

Reference yield:

1-bromomethyl-3-trifluoromethylbenzene (402-23-3) → 1-(3-(trifluoromethyl)benzyl)-1H-pyrazole-4-carboxylic acid (752222-88-1)

Guidance literature:

Multi-step reaction with 2 steps

1: K₂CO₃ / acetone / 16 h / 50 °C

2: KOH / methanol / 18 h / Heating

With potassium hydroxide; potassium carbonate; In methanol; acetone;

DOI:10.1021/jm051268+

Reference yield:

→ 1-(3-(trifluoromethyl)benzyl)-1H-pyrazole-4-carboxylic acid (752222-88-1)

Guidance literature:

upstream raw materials:

ethyl 1-{[3-(trifluoromethyl)phenyl]methyl}-1H-pyrazole-4-carboxylate

1-bromomethyl-3-trifluoromethylbenzene

Downstream raw materials:

C₁₉H₁₉F₃N₆O₃

C₂₁H₂₃F₃N₆O₃

N-(6-amino-1-methyl-2,4-dioxo-3-(cyclopropylmethyl)(1,3-dihydropyrimidin-5-yl))(1-{[3-(trifluoromethyl)phenyl]methyl}-pyrazol-4-yl)carboxamide

C₂₂H₂₅F₃N₆O₃

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