Page last updated: 2024-11-05

phenyl trifluoromethyl ketone

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Phenyl trifluoromethyl ketone, also known as trifluoroacetophenone, is a colorless liquid with a pungent odor. It is a versatile building block in organic synthesis and finds applications in various fields.

**Synthesis:**
Phenyl trifluoromethyl ketone is typically synthesized via Friedel-Crafts acylation of benzene with trifluoroacetic anhydride in the presence of a Lewis acid catalyst, such as aluminum chloride.

**Effects:**
This compound exhibits a wide range of biological activities, including antibacterial, antifungal, and anti-inflammatory properties. It has been shown to be a potent inhibitor of enzymes such as acetylcholinesterase and lipase.

**Importance:**
Phenyl trifluoromethyl ketone is a valuable intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it a highly sought-after reagent in organic synthesis.

**Why it is studied:**
The compound's diverse biological activities and its role as a versatile synthetic building block make it a subject of ongoing research. Scientists are exploring its potential as a lead compound for drug development and studying its applications in various chemical transformations.

**Other aspects of interest:**
- Phenyl trifluoromethyl ketone is a known irritant and should be handled with caution.
- Its strong electron-withdrawing trifluoromethyl group imparts unique reactivity to the molecule.
- It serves as a precursor for the synthesis of various other fluorinated compounds, which often exhibit enhanced properties.'

phenyl trifluoromethyl ketone: converted to trifluoroacetic acid in water [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID9905
CHEMBL ID293277
SCHEMBL ID33083
MeSH IDM0416287

Synonyms (55)

Synonym
acetophenone, 2,2,2-trifluoro-
ethanone, 2,2,2-trifluoro-1-phenyl-
trifluoroacetophenone ,
phenyl trifluoromethyl ketone
434-45-7
trifluoromethyl phenyl ketone
nsc42752
.alpha.,.alpha.-trifluoroacetophenone
ethanone,2,2-trifluoro-1-phenyl-
2,2-trifluoro-1-phenylethanone
1,1-trifluoroacetophenone
2,2-trifluoroacetophenone
nsc-42752
acetophenone,2,2-trifluoro-
inchi=1/c8h5f3o/c9-8(10,11)7(12)6-4-2-1-3-5-6/h1-5
2,2,2-trifluoroacetophenone, 99%
CHEMBL293277 ,
2,2,2-trifluoro-1-phenylethanone
bdbm50163190
2,2,2-trifluoro-1-phenyl-ethanone
2,2,2-trifluoroacetophenone
T0848
AKOS005254512
2,2,2-trifluoro-1-phenylethan-1-one
EN300-51325
trifluoroacetylbenzene
phenyltrifluoromethylketone
unii-6t7l1upy09
6t7l1upy09 ,
nsc 42752
einecs 207-103-1
alpha,alpha,alpha-trifluoroacetophenone
1,1,1-trifluoroacetophenone
FT-0622080
2,2,2-trifluoro-1-phenyl-1-ethanone
.alpha.,.alpha.,.alpha.-trifluoroacetophenone
.omega.,.omega.,.omega.-trifluoroacetophenone
(trifluoroacetyl)benzene
c8h5f3o
SCHEMBL33083
trifluoromethylphenylketone
trifluoromethylphenyl ketone
DTXSID6059992
W-106226
mfcd00000420
2,2,2-trifluoroacetophenone, 98%
F16442
F0001-1195
CS-0031430
STL444353
2,2,2-trifluroacetophenone
AMY8875
Q27265490
A934241
Z649458352
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (2)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Fatty-acid amide hydrolase 1Homo sapiens (human)IC50 (µMol)100.00000.00020.59827.0000AID241449
Liver carboxylesterase 1Homo sapiens (human)IC50 (µMol)0.00400.00400.25510.6000AID241415
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (20)

Processvia Protein(s)Taxonomy
fatty acid catabolic processFatty-acid amide hydrolase 1Homo sapiens (human)
arachidonic acid metabolic processFatty-acid amide hydrolase 1Homo sapiens (human)
positive regulation of vasoconstrictionFatty-acid amide hydrolase 1Homo sapiens (human)
monoacylglycerol catabolic processFatty-acid amide hydrolase 1Homo sapiens (human)
cholesterol biosynthetic processLiver carboxylesterase 1Homo sapiens (human)
cholesterol metabolic processLiver carboxylesterase 1Homo sapiens (human)
response to toxic substanceLiver carboxylesterase 1Homo sapiens (human)
positive regulation of cholesterol effluxLiver carboxylesterase 1Homo sapiens (human)
negative regulation of cholesterol storageLiver carboxylesterase 1Homo sapiens (human)
epithelial cell differentiationLiver carboxylesterase 1Homo sapiens (human)
cholesterol homeostasisLiver carboxylesterase 1Homo sapiens (human)
reverse cholesterol transportLiver carboxylesterase 1Homo sapiens (human)
medium-chain fatty acid metabolic processLiver carboxylesterase 1Homo sapiens (human)
regulation of bile acid biosynthetic processLiver carboxylesterase 1Homo sapiens (human)
cellular response to cholesterolLiver carboxylesterase 1Homo sapiens (human)
cellular response to low-density lipoprotein particle stimulusLiver carboxylesterase 1Homo sapiens (human)
cholesterol ester hydrolysis involved in cholesterol transportLiver carboxylesterase 1Homo sapiens (human)
positive regulation of cholesterol metabolic processLiver carboxylesterase 1Homo sapiens (human)
regulation of bile acid secretionLiver carboxylesterase 1Homo sapiens (human)
lipid catabolic processLiver carboxylesterase 1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (10)

Processvia Protein(s)Taxonomy
protein bindingFatty-acid amide hydrolase 1Homo sapiens (human)
phospholipid bindingFatty-acid amide hydrolase 1Homo sapiens (human)
fatty acid amide hydrolase activityFatty-acid amide hydrolase 1Homo sapiens (human)
identical protein bindingFatty-acid amide hydrolase 1Homo sapiens (human)
acylglycerol lipase activityFatty-acid amide hydrolase 1Homo sapiens (human)
amidase activityFatty-acid amide hydrolase 1Homo sapiens (human)
sterol esterase activityLiver carboxylesterase 1Homo sapiens (human)
methylumbelliferyl-acetate deacetylase activityLiver carboxylesterase 1Homo sapiens (human)
carboxylesterase activityLiver carboxylesterase 1Homo sapiens (human)
carboxylic ester hydrolase activityLiver carboxylesterase 1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (8)

Processvia Protein(s)Taxonomy
endoplasmic reticulum membraneFatty-acid amide hydrolase 1Homo sapiens (human)
cytoskeletonFatty-acid amide hydrolase 1Homo sapiens (human)
organelle membraneFatty-acid amide hydrolase 1Homo sapiens (human)
cytoplasmLiver carboxylesterase 1Homo sapiens (human)
endoplasmic reticulumLiver carboxylesterase 1Homo sapiens (human)
endoplasmic reticulum lumenLiver carboxylesterase 1Homo sapiens (human)
lipid dropletLiver carboxylesterase 1Homo sapiens (human)
cytosolLiver carboxylesterase 1Homo sapiens (human)
lipid dropletLiver carboxylesterase 1Homo sapiens (human)
endoplasmic reticulumLiver carboxylesterase 1Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (14)

Assay IDTitleYearJournalArticle
AID85243In vitro cytotoxic activity against human squamous cell carcinoma (HSC-2) cells.1999Bioorganic & medicinal chemistry letters, Nov-01, Volume: 9, Issue:21
Alpha-trifluoromethylated acyloins induce apoptosis in human oral tumor cell lines.
AID1110768Inhibition of juvenile hormone esterase2003Bioorganic & medicinal chemistry, Nov-17, Volume: 11, Issue:23
Use of classical and 3-D QSAR to examine the hydration state of juvenile hormone esterase inhibitors.
AID1594613Reversible drug reactivity against cysteine in PBS buffer by NMR assay2019Bioorganic & medicinal chemistry, 05-15, Volume: 27, Issue:10
Characterising covalent warhead reactivity.
AID239671Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coli; ND: Not determined2005Journal of medicinal chemistry, Mar-24, Volume: 48, Issue:6
Discovery of a potent, selective, and efficacious class of reversible alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics.
AID1594609Drug reactivity against cysteine in PBS buffer by NMR assay2019Bioorganic & medicinal chemistry, 05-15, Volume: 27, Issue:10
Characterising covalent warhead reactivity.
AID1594614Reversible drug reactivity against serine in PBS buffer by NMR assay2019Bioorganic & medicinal chemistry, 05-15, Volume: 27, Issue:10
Characterising covalent warhead reactivity.
AID82566In vitro cytotoxic activity against human gingival fibroblasts (HGF).1999Bioorganic & medicinal chemistry letters, Nov-01, Volume: 9, Issue:21
Alpha-trifluoromethylated acyloins induce apoptosis in human oral tumor cell lines.
AID1413064Inhibition of full length recombinant human HDAC6 at 10 uM using Fluor-de-Lys deacetylase as substrate preincubated for 15 mins followed by substrate addition and measured after 60 mins by spectrofluorimetric method relative to control2018MedChemComm, Jun-01, Volume: 9, Issue:6
Assessment of the trifluoromethyl ketone functionality as an alternative zinc-binding group for selective HDAC6 inhibition.
AID85248In vitro cytotoxic activity against human salivary gland tumor (HSG) cells.1999Bioorganic & medicinal chemistry letters, Nov-01, Volume: 9, Issue:21
Alpha-trifluoromethylated acyloins induce apoptosis in human oral tumor cell lines.
AID88249In vitro inhibitory activity evaluated against Helicobacter pylori (HP)1999Bioorganic & medicinal chemistry letters, Jan-18, Volume: 9, Issue:2
In vitro susceptibility of Helicobacter pylori to trifluoromethyl ketones.
AID1594610Drug reactivity against serine in PBS buffer by NMR assay2019Bioorganic & medicinal chemistry, 05-15, Volume: 27, Issue:10
Characterising covalent warhead reactivity.
AID242589Inhibitory concentration against KIAA1363 hydrolase2005Journal of medicinal chemistry, Mar-24, Volume: 48, Issue:6
Discovery of a potent, selective, and efficacious class of reversible alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics.
AID241449Inhibitory concentration against Fatty-acid amide hydrolase2005Journal of medicinal chemistry, Mar-24, Volume: 48, Issue:6
Discovery of a potent, selective, and efficacious class of reversible alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics.
AID241415Inhibitory concentration against Triacylglycerol hydrolase2005Journal of medicinal chemistry, Mar-24, Volume: 48, Issue:6
Discovery of a potent, selective, and efficacious class of reversible alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's2 (25.00)18.2507
2000's4 (50.00)29.6817
2010's2 (25.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.35

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.35 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index4.55 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.35)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]