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Thermo Scientific Chemicals
4-Fluorobenzotrifluoride, 98+%
CAS: 402-44-8 | C7H4F4 | 164.103 g/mol
化学物質識別子
CAS402-44-8
IUPAC Name1-fluoro-4-(trifluoromethyl)benzene
Molecular FormulaC7H4F4
InChI KeyUNNNAIWPDLRVRN-UHFFFAOYSA-N
SMILESFC1=CC=C(C=C1)C(F)(F)F
さらに表示
仕様
スペックシート
スペックシートAssay (GC)≥98.0%
Refractive Index1.3995-1.4035 @ 20?C
Appearance (Color)Clear colorless
FormLiquid
4-Fluorobenzotrifluoride was used in the synthesis of 2,2?-bis(trifluoromethylphenoxy)biphenyl via nucleophilic aromatic substitution reaction with 2,2?-biphenol, (S)-fluoxetine, potent inhibitor of neuronal serotonin-uptake and 1-aryloxy-2-substituted aminomethyltetrahydronaphthalene derivatives.
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 Scientific Chemicals.
Applications
4-Fluorobenzotrifluoride was used in the synthesis of 2,2′-bis(trifluoromethylphenoxy)biphenyl via nucleophilic aromatic substitution reaction with 2,2′-biphenol, (S)-fluoxetine, potent inhibitor of neuronal serotonin-uptake and 1-aryloxy-2-substituted aminomethyltetrahydronaphthalene derivatives.
Solubility
Slightly soluble in water.
Notes
Store in cool, dry place in tightly closed container. Store away from oxidizing agent.
4-Fluorobenzotrifluoride was used in the synthesis of 2,2′-bis(trifluoromethylphenoxy)biphenyl via nucleophilic aromatic substitution reaction with 2,2′-biphenol, (S)-fluoxetine, potent inhibitor of neuronal serotonin-uptake and 1-aryloxy-2-substituted aminomethyltetrahydronaphthalene derivatives.
Solubility
Slightly soluble in water.
Notes
Store in cool, dry place in tightly closed container. Store away from oxidizing agent.
RUO – Research Use Only
General References:
- Akiko Okamoto; Katsuya Maeyama; Keiichi Noguchi; Hideaki Oike; Yoshihiko Murakami; Noriyuki Yonezawa. Synthesis of novel trifluoromethyl-bearing bifunctional acyl-acceptant arenes: 2,2'-bis(trifluoromethylated aryloxy)biphenyls. Journal of Oleo Science,. 2007, 56 (9),479-491.
- D W Robertson et. al. Absolute configurations and pharmacological activities of the optical isomers of fluoxetine, a selective serotonin-uptake inhibitor. Journal of Medicinal Chemistry, 1988, 31 (7), 1412-1417.