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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
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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
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Safety

HS Code 
2906190090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Activate Scientific
Product number
AS46451
Product name
trans-4-(Trifluoromethyl)cyclohexanol
Purity
97%
Packaging
250mg
Price
$176
Updated
2021/12/16
Activate Scientific
Product number
AS46451
Product name
trans-4-(Trifluoromethyl)cyclohexanol
Purity
97%
Packaging
1g
Price
$358
Updated
2021/12/16
AK Scientific
Product number
9829AL
Product name
trans-4-(Trifluoromethyl)cyclohexanol
Packaging
5g
Price
$979
Updated
2021/12/16
Activate Scientific
Product number
AS46451
Product name
trans-4-(Trifluoromethyl)cyclohexanol
Purity
97%
Packaging
5G
Price
$1127
Updated
2021/12/16
Chemenu
Product number
CM129406
Product name
trans-4-(Trifluoromethyl)cyclohexanol
Purity
98%
Packaging
10g
Price
$1244
Updated
2021/12/16
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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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75091-93-9, trans-4-(Trifluoromethyl)cyclohexanol Related Search:


  • trans-4-(Trifluoromethyl)cyclohexanol
  • trans (e,e)-4-trifluoromethylcyclohexanol
  • trans-4-(Trifluoromethyl)
  • Cyclohexanol, 4-(trifluoromethyl)-, trans-
  • Trans-4-(Trifluoromethyl)Cyclohexano
  • 75091-93-9