75091-99-5
- Product Name：4-(trifluoromethyl)cyclohexanone
- Molecular Formula：C7H9F3O
- Purity：99%
- Molecular Weight：166.143
Product Details;
CasNo： 75091-99-5
Molecular Formula： C7H9F3O
Chinese Factory Supply Top Purity 99% 4-(trifluoromethyl)cyclohexanone 75091-99-5 On Stock
- Molecular Formula:C7H9F3O
- Molecular Weight:166.143
- Vapor Pressure:2.916mmHg at 25°C
- Refractive Index:1.395
- Boiling Point:156.246 °C at 760 mmHg
- Flash Point:53.308 °C
- PSA：17.07000
- Density:1.221 g/cm3
- LogP:2.30800
4-(TRIFLUOROMETHYL)CYCLOHEXANONE(Cas 75091-99-5) Usage
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Uses |
4-(Trifluoromethyl)cyclohexanone (cas# 75091-99-5) is a compound useful in organic synthesis. |
InChI:InChI=1/C7H9F3O/c8-7(9,10)5-1-3-6(11)4-2-5/h5H,1-4H2
75091-99-5 Relevant articles
Synthesis method of 4-substituent cyclohexanone liquid crystal intermediate
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Paragraph 0056-0058, (2021/05/19)
The invention discloses a synthesis meth...
Csp3-H Trifluoromethylation of Unactivated Aliphatic Systems
He, Jiachen,Nguyen, Truong N.,Guo, Shuo,Cook, Silas P.
supporting information, p. 702 - 705 (2021/02/01)
A straightforward method for the undirec...
Direct C(sp3)?H Trifluoromethylation of Unactivated Alkanes Enabled by Multifunctional Trifluoromethyl Copper Complexes
Choi, Geunho,Lee, Geun Seok,Park, Beomsoon,Kim, Dongwook,Hong, Soon Hyeok
supporting information, p. 5467 - 5474 (2021/01/20)
A mild and operationally simple C(sp3)?H...
Aliphatic C-H Bond Oxidation with Hydrogen Peroxide Catalyzed by Manganese Complexes: Directing Selectivity through Torsional Effects
Milan, Michela,Bietti, Massimo,Costas, Miquel
supporting information, p. 2720 - 2723 (2018/05/22)
Substituted N-cyclohexyl amides undergo ...
75091-99-5 Process route
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- 75091-92-8,75091-93-9,30129-18-1
4-(trifluoromethyl)cyclohexan-1-ol
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- 75091-99-5
4-(trifluoromethyl)cyclohexan-1-one
| Conditions | Yield |
|---|---|
|
With Dess-Martin periodane; In dichloromethane; at 20 ℃; for 2h;
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94.6% |
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4-(trifluoromethyl)cyclohexan-1-ol; With C10H20NO2(1-); sodium hydrogencarbonate; In chloroform; water; at 20 ℃; for 0.25h;
With trichloroisocyanuric acid; In chloroform; water; for 6h;
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88.5% |
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With pyridinium chlorochromate; In dichloromethane; at 20 ℃; for 2h;
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57% |
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With CrO3/silica gel; In various solvent(s); at 40 ℃; for 4h; under 165013 Torr;
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46 % Chromat. |
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C12H20F3NO
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N-(4-(trifluoromethyl)cyclohexyl)pivalamide
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- 75091-99-5
4-(trifluoromethyl)cyclohexan-1-one
| Conditions | Yield |
|---|---|
|
With C40H68F6MnN4O6S2Si2; dihydrogen peroxide; acetic acid; In acetonitrile; at -40 ℃; for 0.5h; diastereoselective reaction;
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96% |
75091-99-5 Upstream products
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2-trimethylsilyloxy-1,3-butadiene
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75091-92-8
4-(trifluoromethyl)cyclohexan-1-ol
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401-75-2
trifluoromethylcyclohexane
75091-99-5 Downstream products
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683242-93-5
4,4,5,5-tetramethyl-2-(4-(trifluoromethyl)cyclohex-1-en-1-yl)-1,3,2-dioxaborolane
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-
951671-02-6
4,4'-[4-(trifluoromethyl)cyclohexane-1,1-diyl]diphenol
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1156679-69-4
N-ethyl-4-(trifluoromethyl)cyclohexanamine
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