CAS 444-29-1
:1-Iodo-2-(trifluoromethyl)benzene
Description:
1-Iodo-2-(trifluoromethyl)benzene, with the CAS number 444-29-1, is an aromatic compound characterized by the presence of an iodine atom and a trifluoromethyl group (-CF3) attached to a benzene ring. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is known for its relatively high density and low solubility in water, making it more soluble in organic solvents. The presence of the trifluoromethyl group imparts unique electronic properties, enhancing its reactivity in various chemical reactions, particularly in nucleophilic substitution and electrophilic aromatic substitution. Additionally, the iodine atom can serve as a leaving group in reactions, facilitating the synthesis of other compounds. Due to its halogenated nature, 1-iodo-2-(trifluoromethyl)benzene may exhibit biological activity and is of interest in medicinal chemistry and materials science. Proper handling and storage are essential, as it may pose health and environmental risks.
Formula:C7H4F3I
InChI:InChI=1/C7H4F3I/c8-7(9,10)5-3-1-2-4-6(5)11/h1-4H
InChI key:InChIKey=IGZGUYVVBABKOY-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(I)C=CC=C1
Synonyms:- .alpha.,.alpha.,.alpha.-Trifluoro-o-iodo toluene
- 1-Iod-2-(trifluormethyl)benzol
- 1-Iodo-2-(trifluoromethyl)benzene
- 1-Trifluoromethyl-2-iodobenzene
- 2-(Trifluoromethyl)iodobenzene
- 2-Iodo-1-trifluoromethylbenzene
- 2-Iodobenzotrifluoride
- 2-Trifluoromethylphenyl iodide
- Benzene, 1-iodo-2- (trifluoromethyl)-
- NSC 88291
- Toluene, alpha,alpha,alpha-trifluoro-o-iodo-
- Toluene, α,α,α-trifluoro-o-iodo-
- alpha,alpha,alpha-Trifluoro-2-iodotoluene
- o-(Trifluoromethyl)iodobenzene
- o-Iodobenzotrifluoride
- o-Trifluoromethyliodobenzene
- α,α,α-Trifluoro-o-iodotoluene
- 2-(Trifluoromethyl)iodobenzene, 2-Iodo-α,α,α-trifluorotoluene
- 2-Trifluoromethyliodobenzene
- 2-Iodobenztrifluoride
- 2-Iodobenzotrifluoride (stabilized with Copper chip)
- 2-IODOBENZOTRIFLUORIDE 99%
- alpha,alpha,alpha-Trifluoro-o-iodotoluene
- o-Iodo-alpha,alpha,alpha-trifluorotoluene
- 2-Iodobenzotrifluoride,99%
- 1-iodo-2-(trifluoromethyl)-benzen
- 2-IODO-ALPHA,ALPHA,ALPHA-TRIFLUOROTOLUENE
- O-IODINE TRIFLUORO TOLUENE
- See more synonyms
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Found 7 products.
2-Iodobenzotrifluoride (stabilized with Copper chip)
CAS:Formula:C7H4F3IPurity:>98.0%(GC)Color and Shape:Colorless to Light orange to Yellow clear liquidMolecular weight:272.012-Iodobenzotrifluoride, 99%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formula:C7H4F3IPurity:99%Color and Shape:Liquid, Clear colorless to yellow or pale greenMolecular weight:272.012-Iodobenzotrifluoride
CAS:2-IodobenzotrifluorideFormula:C7H4F3IPurity:98%Color and Shape: colourless to light yellow liquidMolecular weight:272.01g/mol2-Iodobenzotrifluoride
CAS:2-Iodobenzotrifluoride is a chemical compound that inhibits protein synthesis by binding to the aryl boronic acid groups of proteins. This compound also has anti-inflammatory properties and can be used as a control agent for inflammatory diseases. 2-Iodobenzotrifluoride is soluble in hydrocarbon solvents and reacts with sodium ions to produce sodium-dependent glucose, which can be used as an energy source for cells. The trifluoromethyl group of 2-iodobenzotrifluoride binds to the amino acids serine and histidine, inhibiting their activity. It also inhibits other enzymes such as cholesteryl ester transfer protein and carbonic anhydrase, which are involved in the production of cholesterol. 2-Iodobenzotrifluoride is also able to inhibit nucleophilic groups such as cysteine thiols (SH) and glutFormula:C7H4F3IPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:272.01 g/mol2-Iodobenzotrifluoride
CAS:Controlled ProductApplications 2-Iodobenzotrifluoride acts as a reagent in the preparation, cyclooxygenase-1 inhibitory activity, and docking studies of aminoalkoxyphenylbenzamides. Prepartion and SAR of tricyclic 4,4-dimethyl-3,4-dihydrochromeno[3,4-d]imidazole derivatives as microsomal prostaglandin E2 synthase-1 (mPGES-1) inhibitors.
References Fukai, R., et al.: ChemMedChem, 6, 550 (2011); Muthukaman, N., et al.: Bioorg. Med. Chem. Lett., 27, 2594 (2017)Formula:C7H4F3IColor and Shape:NeatMolecular weight:272.01






