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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
Molecular Weight:
168.16
MDL Number:
MFCD12964322
MOL File:
75091-93-9.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:54

trans-4-(Trifluoromethyl)cyclohexanol Properties

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

Risk and Safety Statements

HS Code  2906190090

trans-4-(Trifluoromethyl)cyclohexanol price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Activate Scientific AS46451 trans-4-(Trifluoromethyl)cyclohexanol 97% 75091-93-9 250mg $176 2021-12-16 Buy
Activate Scientific AS46451 trans-4-(Trifluoromethyl)cyclohexanol 97% 75091-93-9 1g $358 2021-12-16 Buy
AK Scientific 9829AL trans-4-(Trifluoromethyl)cyclohexanol 75091-93-9 5g $979 2021-12-16 Buy
Activate Scientific AS46451 trans-4-(Trifluoromethyl)cyclohexanol 97% 75091-93-9 5G $1127 2021-12-16 Buy
Chemenu CM129406 trans-4-(Trifluoromethyl)cyclohexanol 98% 75091-93-9 10g $1244 2021-12-16 Buy
Product number Packaging Price Buy
AS46451 250mg $176 Buy
AS46451 1g $358 Buy
9829AL 5g $979 Buy
AS46451 5G $1127 Buy
CM129406 10g $1244 Buy

trans-4-(Trifluoromethyl)cyclohexanol Chemical Properties,Uses,Production

Synthesis

4-Trifluoromethylphenol

402-45-9

cis-4-(Trifluoromethyl)cyclohexanol

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

trans-4-(Trifluoromethyl)cyclohexanol Suppliers

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trans-4-(Trifluoromethyl)cyclohexanol Spectrum

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