7731-29-5

  • Product Name:TRANS-4-METHYLCYCLOHEXANOL
  • Molecular Formula:C7H14 O
  • Purity:99%
  • Molecular Weight:114.188
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Product Details;

CasNo: 7731-29-5

Molecular Formula: C7H14 O

Buy Quality Top Purity 99% TRANS-4-METHYLCYCLOHEXANOL 7731-29-5 Cheapest Price

  • Molecular Formula:C7H14 O
  • Molecular Weight:114.188
  • Melting Point:-9.2°C (estimate) 
  • Refractive Index:n20/D 1.455(lit.) 
  • Boiling Point:173-175 °C(lit.)  
  • PKA:15.32±0.40(Predicted) 
  • Flash Point:158 °F  
  • PSA:20.23000 
  • Density:0.912 g/mL at 25 °C(lit.)  
  • LogP:1.55740 

TRANS-4-METHYLCYCLOHEXANOL(Cas 7731-29-5) Usage

Chemical Properties

CLEAR COLOURLESS LIQUID

Uses

trans-4-Methylcyclohexanol is used to prepare 4-methylcyclohexyl nitrite to study the laser-induced fluorescence (LIF) excitation spectra of the 4-methylcyclohexoxy and d11-cyclohexoxy radicals.

General Description

trans-4-Methylcyclohexanol is an active Aedes triseriatus oviposition attractant.

Biochem/physiol Actions

trans-4-Methylcyclohexanol is the major metabolite formed by biological regioselective reduction of 4-methylcyclohexanone by Glomerella cingulata.

InChI:InChI=1/C7H14O/c1-6-2-4-7(8)5-3-6/h6-8H,2-5H2,1H3/t6-,7-

7731-29-5 Relevant articles

Correction - Conformational Analysis. V. The Reaction of cis-and trans-4-t-Butylcyclohexanol and trans-4-Methylcyclohexanol with Phosphorus Pentabromide. Synthesis of Alkylcyclohexyl Bromides

Ernest Eliel and Ralph Haber

, J. Org. Chem. 1959, 24, 12, 2074

ConformationalAnalysis.V,The Reaction of cis- and trans-4-t-Butylcyclohexanol and TRANS-4-METHYLCYCLOHEXANOL with Phosphorus Pentahromide.Synthesis of Alkylcyclohexyl Bromides.

Trans-Selective and Switchable Arene Hydrogenation of Phenol Derivatives

Bergander, Klaus,Glorius, Frank,Heusler, Arne,Wollenburg, Marco

, p. 11365 - 11370 (2020/11/24)

A trans-selective arene hydrogenation of...

SN2 Reaction of Diarylmethyl Anions at Secondary Alkyl and Cycloalkyl Carbons

Shinohara, Riku,Ogawa, Narihito,Kawashima, Hidehisa,Wada, Kyohei,Saito, Shun,Yamazaki, Takashi,Kobayashi, Yuichi

, p. 1461 - 1478 (2019/01/25)

The substitution reaction of the diethyl...

Cobalt-Nanoparticles Catalyzed Efficient and Selective Hydrogenation of Aromatic Hydrocarbons

Murugesan, Kathiravan,Senthamarai, Thirusangumurugan,Alshammari, Ahmad S.,Altamimi, Rashid M.,Kreyenschulte, Carsten,Pohl, Marga-Martina,Lund, Henrik,Jagadeesh, Rajenahally V.,Beller, Matthias

, p. 8581 - 8591 (2019/09/12)

The development of inexpensive and pract...

7731-29-5 Process route

methyl cyclohexane
82166-21-0

methyl cyclohexane

1-Methylcyclohexanol
590-67-0

1-Methylcyclohexanol

trans-4-methylcyclohexan-1-ol
7731-29-5

trans-4-methylcyclohexan-1-ol

cis-4-methylcyclohexanol
7731-28-4

cis-4-methylcyclohexanol

(+/-)-trans-2-methylcyclohexanol
7443-52-9

(+/-)-trans-2-methylcyclohexanol

cis-2-methylcyclohexanol
7443-70-1

cis-2-methylcyclohexanol

rac-trans-3-methylcyclohexanol
7443-55-2

rac-trans-3-methylcyclohexanol

cis-3-methylcyclohexanol
5454-79-5

cis-3-methylcyclohexanol

1-methylcyclohexan-4-one
589-92-4

1-methylcyclohexan-4-one

2-Methylcyclohexanone
583-60-8

2-Methylcyclohexanone

cyclohexylmethyl alcohol
100-49-2

cyclohexylmethyl alcohol

cyclohexanecarbaldehyde
2043-61-0

cyclohexanecarbaldehyde

3-Methylcyclohexanone
591-24-2,625-96-7

3-Methylcyclohexanone

Conditions
Conditions Yield
With C22H17BClF9N6NiO3; at 70 ℃; for 6h; Inert atmosphere;
0.36 mmol
0.52 mmol
2.31 mmol
0.08 mmol
0.27 mmol
0.42 mmol
0.72 mmol
0.32 mmol
1.46 mmol
0.17 mmol
0.36 mmol
0.52 mmol
With [(PhSiO1.5)12(CuO)4(NaO0.5)4]; dihydrogen peroxide; nitric acid; In acetonitrile; at 60 ℃; Reagent/catalyst;
 
With 12(C6H5SiO1.5)*6Ni(2+)*6O(2-)*Na(1+)*Cl(1-)*13C4H8O2*2C7H5N*2H2O; nitric acid; 3-chloro-benzenecarboperoxoic acid; at 60 ℃; for 3h;
 
methyl cyclohexane
82166-21-0

methyl cyclohexane

1-Methylcyclohexanol
590-67-0

1-Methylcyclohexanol

(1R,2R)-(-)-trans-2-methylcyclohexanol
19043-03-9

(1R,2R)-(-)-trans-2-methylcyclohexanol

(1R,2S)-2-methylcyclohexanol
583-59-5,615-38-3,615-39-4,7443-52-9,7443-70-1,15963-35-6,15963-37-8,19043-02-8,19043-03-9

(1R,2S)-2-methylcyclohexanol

(3R,1R)-3-methylcyclohexanol
24965-94-4

(3R,1R)-3-methylcyclohexanol

trans-4-methylcyclohexan-1-ol
7731-29-5

trans-4-methylcyclohexan-1-ol

cis-4-methylcyclohexanol
7731-28-4

cis-4-methylcyclohexanol

cis-3-methylcyclohexanol
24965-91-1

cis-3-methylcyclohexanol

1-methylcyclohexan-4-one
589-92-4

1-methylcyclohexan-4-one

2-Methylcyclohexanone
583-60-8

2-Methylcyclohexanone

cyclohexylmethyl alcohol
100-49-2

cyclohexylmethyl alcohol

cyclohexanecarbaldehyde
2043-61-0

cyclohexanecarbaldehyde

3-Methylcyclohexanone
591-24-2,625-96-7

3-Methylcyclohexanone

Conditions
Conditions Yield
With cis-(Cl,Cl)-[Re(p-NC6H4CH3)Cl2(indazole-3-carboxylate)(P(phenyl)3)] methanol solvate; dihydrogen peroxide; In water; acetonitrile; Catalytic behavior;
 

7731-29-5 Upstream products

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    piperonal

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    620-92-8

    bis-(4-hydroxyphenyl)methane

7731-29-5 Downstream products

  • 1123-25-7
    1123-25-7

    1-methyl-1-cyclohexanecarboxylic acid

  • 931-68-0
    931-68-0

    1-chloro-4-methylcyclohexane

  • 28046-90-4
    28046-90-4

    cis-1-bromo-4-methylcyclohexane

  • 1161-20-2
    1161-20-2

    3,5-dinitro-benzoic acid-(trans-4-methyl-cyclohexyl ester)

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