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Merck
CN

195359

Sigma-Aldrich

对氟三氟甲苯

98%

别名:

α,α,α,4-四氟甲苯

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About This Item

线性分子式:
FC6H4CF3
CAS号:
分子量:
164.10
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

98%

表单

liquid

折射率

n20/D 1.401 (lit.)

沸点

102-105 °C (lit.)

mp

−42-−41.7 °C (lit.)

密度

1.293 g/mL at 25 °C (lit.)

官能团

fluoro

SMILES字符串

Fc1ccc(cc1)C(F)(F)F

InChI

1S/C7H4F4/c8-6-3-1-5(2-4-6)7(9,10)11/h1-4H

InChI key

UNNNAIWPDLRVRN-UHFFFAOYSA-N

应用

对氟三氟甲苯可用于合成:
  • 与2,2′-双酚经亲核芳香取代反应制备2,2′-(三氟甲苯氧基)双苯
  • (S)-氟西汀,神经元血清素摄取的强效抑制剂
  • 1-芳氧基-2-取代氨甲基四氢萘衍生物

象形图

FlameExclamation mark

警示用语:

Danger

危险分类

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

51.8 °F - closed cup

闪点(°C)

11 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Kalpana Bhandari et al.
Bioorganic & medicinal chemistry, 14(8), 2535-2544 (2005-12-13)
Several 1-aryloxy-2-substituted aminomethyltetrahydronaphthalenes (7-21) as conformationally rigid analogues of fluoxetine were synthesized and evaluated for their anorexigenic and antidepressant activities. For SAR studies the related acyclic analogues (22-27) were also prepared. Out of the 21 synthesized compounds, 10 compounds (9
D W Robertson et al.
Journal of medicinal chemistry, 31(7), 1412-1417 (1988-07-01)
Fluoxetine is a potent and selective inhibitor of the neuronal serotonin-uptake carrier and is a clinically effective antidepressant. Although fluoxetine is used therapeutically as the racemate, there appears to be a small but demonstrable stereospecificity associated with its interactions with
Akiko Okamoto et al.
Journal of oleo science, 56(9), 479-491 (2007-09-28)
Novel bifunctional acyl-acceptant biphenyls bearing trifluoromethylated aroyloxy groups were successfully synthesized in high yields via TfOH-mediated electrophilic aromatic aroylation of fluorobenzene with CF(3)-bearing aroyl chlorides followed by nucleophilic aromatic substitution with 2,2'-biphenol. Similarly, 2,2'-bis(trifluoromethylphenoxy)biphenyl was synthesized via nucleophilic aromatic substitution

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