trans-4-(Trifluoromethyl)cyclohexanol
- Product Name
- trans-4-(Trifluoromethyl)cyclohexanol
- CAS No.
- 75091-93-9
- Chemical Name
- trans-4-(Trifluoromethyl)cyclohexanol
- Synonyms
- trans-4-(Trifluoromethyl);Trans-4-(Trifluoromethyl)Cyclohexano;trans-4-(Trifluoromethyl)cyclohexanol;trans (e,e)-4-trifluoromethylcyclohexanol;Cyclohexanol, 4-(trifluoromethyl)-, trans-
- CBNumber
- CB5947269
- Molecular Formula
- C7H11F3O
- Formula Weight
- 168.16
- MOL File
- 75091-93-9.mol
trans-4-(Trifluoromethyl)cyclohexanol Property
- Boiling point:
- 160.4±35.0 °C(Predicted)
- Density
- 1.231±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- 14.88±0.40(Predicted)
- Appearance
- Colorless to light yellow Solid
- InChI
- InChI=1S/C7H11F3O/c8-7(9,10)5-1-3-6(11)4-2-5/h5-6,11H,1-4H2/t5-,6-
- InChIKey
- VJUJYNJEPPWWHS-IZLXSQMJSA-N
- SMILES
- [C@@H]1(O)CC[C@@H](C(F)(F)F)CC1
Safety
- HS Code
- 2906190090
N-Bromosuccinimide Price
- Product number
- AS46451
- Product name
- trans-4-(Trifluoromethyl)cyclohexanol
- Purity
- 97%
- Packaging
- 250mg
- Price
- $176
- Updated
- 2021/12/16
- Product number
- AS46451
- Product name
- trans-4-(Trifluoromethyl)cyclohexanol
- Purity
- 97%
- Packaging
- 1g
- Price
- $358
- Updated
- 2021/12/16
- Product number
- 9829AL
- Product name
- trans-4-(Trifluoromethyl)cyclohexanol
- Packaging
- 5g
- Price
- $979
- Updated
- 2021/12/16
- Product number
- AS46451
- Product name
- trans-4-(Trifluoromethyl)cyclohexanol
- Purity
- 97%
- Packaging
- 5G
- Price
- $1127
- Updated
- 2021/12/16
- Product number
- CM129406
- Product name
- trans-4-(Trifluoromethyl)cyclohexanol
- Purity
- 98%
- Packaging
- 1g
- Price
- $252
- Updated
- 2021/12/16
trans-4-(Trifluoromethyl)cyclohexanol Chemical Properties,Usage,Production
Synthesis
402-45-9
75091-92-8
Step A: Synthesis of 4-trifluoromethylcyclohexanol; 4-hydroxytrifluorotoluene (5 g, 30.8 mmol) was placed in an autoclave reactor, dissolved in acetic acid (15 ml) and platinum oxide (PtO, 500 mg) was added as a catalyst. The reactor was pressurized using hydrogen (50 psi) and the reaction was carried out for 16 h at room temperature. Upon completion of the reaction, the reaction mixture was filtered through a bed of diatomaceous earth and the filtrate was neutralized with 1N sodium hydroxide solution and subsequently extracted with diethyl ether. The organic phase was dried over anhydrous magnesium sulfate (MgSO4) and concentrated in vacuum at room temperature to give trans-4-(trifluoromethyl)cyclohexanol (4.5 g, 87% yield). MS [M + H]+ = 169 (corresponding to M + 1).
References
[1] Patent: WO2008/7930, 2008, A1. Location in patent: Page/Page column 27
[2] Journal of Organic Chemistry USSR (English Translation), 1970, vol. 6, # 10, p. 2063 - 2067
[3] Zhurnal Organicheskoi Khimii, 1970, vol. 6, # 10, p. 2055 - 2060
trans-4-(Trifluoromethyl)cyclohexanol Preparation Products And Raw materials
Raw materials
Preparation Products
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