8-(Trifluoromethyl)quinoline-3-carboxylic acid

Base Information

• Chemical Name: 8-(Trifluoromethyl)quinoline-3-carboxylic acid
• CAS No.: 31588-79-1
• Molecular Formula: C11H6F3NO2
• Molecular Weight: 241.17
• ChEMBL ID: CHEMBL3228138
• DSSTox Substance ID: DTXSID10562886
• Wikidata: Q82447177
• Mol file: 31588-79-1.mol

Synonyms:8-(TRIFLUOROMETHYL)QUINOLINE-3-CARBOXYLIC ACID;31588-79-1;CHEMBL3228138;DTXSID10562886;SFGJRDPCPWCNMJ-UHFFFAOYSA-N;AMY26446;MFCD11557213;AKOS023554331;SB72069;AS-41968;CS-0197143;A849935;8-(TRIFLUOROMETHYL)QUINOLINE-3-CARBOXYLICACID

Chemical Property of 8-(Trifluoromethyl)quinoline-3-carboxylic acid

Chemical Property:

• PSA: 50.19000
• LogP: 2.95180
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 241.03506292
• Heavy Atom Count: 17
• Complexity: 306

Purity/Quality:

97% ^*data from raw suppliers

8-(trifluoromethyl)quinoline-3-carboxylicacid 95 ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC2=CC(=CN=C2C(=C1)C(F)(F)F)C(=O)O

Technology Process of 8-(Trifluoromethyl)quinoline-3-carboxylic acid

There total 6 articles about 8-(Trifluoromethyl)quinoline-3-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: 92.0%

ethyl 8-(trifluoromethyl)quinoline-3-carboxylate (31588-75-7) → 8-(trifluoromethyl)quinoline-3-carboxylic acid (31588-79-1)

Guidance literature:

With water; sodium hydroxide; In ethanol; at 20 ℃; for 2h;

Reference yield:

ethyl 4-chloro-8-(trifluoromethyl)quinoline-3-carboxylate (31602-11-6) → 8-(trifluoromethyl)quinoline-3-carboxylic acid (31588-79-1)

Guidance literature:

Multi-step reaction with 3 steps

1: palladium on activated charcoal; hydrogen / ethanol / 20 °C

2: bromine / pyridine / 1 h / 60 °C

3: sodium hydroxide; water / ethanol / 2 h / 20 °C

With palladium on activated charcoal; water; hydrogen; bromine; sodium hydroxide; In pyridine; ethanol;

Reference yield:

ethyl 4-oxo-8-(trifluoromethyl)-1,4-dihydroquinoline-3-carboxylate → 8-(trifluoromethyl)quinoline-3-carboxylic acid (31588-79-1)

Guidance literature:

Multi-step reaction with 4 steps

1: trichlorophosphate / acetonitrile / 7 h / Reflux

2: palladium on activated charcoal; hydrogen / ethanol / 20 °C

3: bromine / pyridine / 1 h / 60 °C

4: sodium hydroxide; water / ethanol / 2 h / 20 °C

With palladium on activated charcoal; water; hydrogen; bromine; sodium hydroxide; trichlorophosphate; In pyridine; ethanol; acetonitrile;

upstream raw materials:

ethyl 8-(trifluoromethyl)quinoline-3-carboxylate

ethyl 4-chloro-8-(trifluoromethyl)quinoline-3-carboxylate

2-[(2-trifluoromethylphenylamino)methylene]malonic acid diethyl ester

2-(trifluoromethyl)benzenamine

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