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2-Methylcyclohexanol

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Name

2-Methylcyclohexanol

EINECS 209-512-0
CAS No. 583-59-5 Density 0.925 g/cm3
PSA 20.23000 LogP 1.55740
Solubility Slightly soluble in water Melting Point -38 °C
Formula C7H14O Boiling Point 170.322 °C at 760 mmHg
Molecular Weight 114.188 Flash Point 58.889 °C
Transport Information UN 2617 3/PG 3 Appearance Colourless viscous liquid with an aromatic odour
Safety 24/25 Risk Codes 20
Molecular Structure Molecular Structure of 583-59-5 (2-Methylcyclohexanol) Hazard Symbols HarmfulXn
Synonyms

1-Methyl-2-cyclohexanol;2-Methyl-1-cyclohexanol;2-Methylcyclohexanol;2-Methylcyclohexyl alcohol;NSC75845;2-Methylcyclohexan-1-ol;

Article Data 266

2-Methylcyclohexanol Synthetic route

583-60-8

2-Methylcyclohexanone

583-59-5

2-Methylcyclohexanol

Conditions
ConditionsYield
With zinc hydride In tetrahydrofuran for 24h; Ambient temperature;100%
With sodium isopropylate; acetonitrile In isopropyl alcohol at 80℃; for 1h; Catalytic behavior;99%
gadolinium(III) isopropoxide In isopropyl alcohol at 30℃; for 1h;98%
218623-12-2

2-(2-methyl-cyclohexyloxy)-tetrahydro-pyran

583-59-5

2-Methylcyclohexanol

Conditions
ConditionsYield
silica-supported prop-1-ylsulfonic acid In methanol99.6%
With sulfuric acid; silica gel In methanol for 0.25h; Heating;80%
With H14[NaP5W30O110] In methanol for 2h; Heating;97 % Chromat.
95-48-7

ortho-cresol

583-59-5

2-Methylcyclohexanol

Conditions
ConditionsYield
With hydrogen In water at 20℃; under 7500.75 Torr; for 6h; Autoclave;99.1%
With hydrogen at 100℃; under 3750.38 Torr; for 3h; Reagent/catalyst; Pressure; Temperature;99%
With nickel(II) oxide; hydrogen; palladium In hexane at 80℃; under 7500.75 Torr; for 10h;98%
583-60-8

2-Methylcyclohexanone

67-63-0

isopropyl alcohol

583-59-5

2-Methylcyclohexanol

Conditions
ConditionsYield
With [{2-(2-pyridyl)benzimidazole}RuCl2(PPh3)2]; potassium hydroxide at 82℃; for 4h;97%
With potassium hydroxide for 4h; Ambient temperature;8%
Mechanism; Product distribution; Irradiation;
1713-33-3

1,2-epoxy-1-methylcyclohexane

583-59-5

2-Methylcyclohexanol

Conditions
ConditionsYield
With sodium tetrahydroborate; triethylamine In water; acetonitrile Irradiation;94%
With cobalt(II) tetrafluoroborate hexahydrate; hydrogen; zinc trifluoromethanesulfonate; [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] In 1,4-dioxane at 60℃; under 30003 Torr; for 20h; Autoclave; regioselective reaction;88 %Chromat.
With ammonia borane; C28H28Cl2CoNP2; erbium(III) triflate In tetrahydrofuran at 55℃; for 8h;89 %Chromat.
5410-22-0

1,2-epoxy-3-methyl-cyclohexane

A

583-59-5

2-Methylcyclohexanol

B

591-23-1

m-methylcyclohexanol

Conditions
ConditionsYield
With Li(1+)*C12H28AlO3(1-) In tetrahydrofuran; hexane at 0℃; for 0.17h; Yields of byproduct given. Title compound not separated from byproducts;A 93%
B n/a
With Li(1+)*C12H28AlO3(1-) In tetrahydrofuran; hexane at 0℃; for 0.17h;A 93%
B n/a
591-49-1

1-methylcyclohex-1-ene

583-59-5

2-Methylcyclohexanol

Conditions
ConditionsYield
Stage #1: 1-methylcyclohex-1-ene With 1-bromo-butane; sodium tetrahydroborate; Aliquat 336 at 20℃; for 16h; Addition; Hydroboration;
Stage #2: With sodium hydroxide; dihydrogen peroxide at 40℃; for 1h; Oxidation;
78%
With sodium tetrahydroborate; (2,3,7,8,12,13,17,18-octaethylporphyrinato)rhodium(III) chloride; oxygen In tetrahydrofuran at 20 - 25℃; for 50h; Product distribution; Mechanism; other olefins, diene and acetylenes, other rhodium porphyrin, other conc. of catalyst;
With sodium tetrahydroborate; oxygen; (2,3,7,8,12,13,17,18-octaethylporphyrinato)rhodium(III) chloride In tetrahydrofuran Ambient temperature; 48-130 h; Yield given;
99522-16-4

2-Trimethylsilanylmethyl-cyclohexanol

583-59-5

2-Methylcyclohexanol

Conditions
ConditionsYield
With potassium tert-butylate; 18-crown-6 ether In water; dimethyl sulfoxide at 80℃; for 12h;78%
106345-17-9

2-(6-Methyl-1-oxa-4-aza-spiro[4.5]dec-4-yl)-ethanol

A

583-59-5

2-Methylcyclohexanol

B

106345-21-5

2-(7-Methyl-4,5,6,7-tetrahydro-indol-1-yl)-ethanol

C

111-42-2

2,2'-iminobis[ethanol]

Conditions
ConditionsYield
With potassium hydroxide Heating; CH3ONa as reagent;A n/a
B 59%
C n/a
101934-18-3

1,5-bis(bromomagnesio)hexane

109-94-4

formic acid ethyl ester

583-59-5

2-Methylcyclohexanol

Conditions
ConditionsYield
In tetrahydrofuran57%

2-Methylcyclohexanol Specification

The 2-Methylcyclohexanol with CAS registry number of 583-59-5 is also known as Cyclohexanol, 2-methyl-. The IUPAC name is 2-Methylcyclohexan-1-ol. It belongs to product categories of Industrial/Fine Chemicals. Its EINECS registry number is 209-512-0. In addition, the formula is C7H14O and the molecular weight is 114.21. This chemical is a colourless viscous liquid with an aromatic odour that may cause damage to health. It is slightly soluble in water and should be sealed in cool, dry place. What's more, this chemical can be used as organic chemical, solvent, lubricant additive, auxiliary and antioxidant. As it is harmful by inhalation, avoid contact with skin and eyes when using it.

Physical properties about 2-Methylcyclohexanol are: (1)ACD/LogP: 1.83; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.83; (4)ACD/LogD (pH 7.4): 1.83; (5)ACD/BCF (pH 5.5): 14.55; (6)ACD/BCF (pH 7.4): 14.55; (7)ACD/KOC (pH 5.5): 236.62; (8)ACD/KOC (pH 7.4): 236.62; (9)#H bond acceptors: 1; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 1; (12)Index of Refraction: 1.462; (13)Molar Refractivity: 33.96 cm3; (14)Molar Volume: 123.4 cm3; (15)Surface Tension: 28.9 dyne/cm; (16)Density: 0.925 g/cm3; (17)Flash Point: 58.9 °C; (18)Enthalpy of Vaporization: 47.36 kJ/mol; (19)Boiling Point: 170.3 °C at 760 mmHg; (20)Vapour Pressure: 0.475 mmHg at 25 °C.

Preparation of 2-Methylcyclohexanol: it is prepared by reaction of 1,2-epoxy-1-methyl-cyclohexane. The reaction needs reagents Et3N, NaBH4 and solvents acetonitrile, H2O with other condition of irradiation. The yield is about 94 %.

2-Methylcyclohexanol is prepared by reaction of 1,2-epoxy-1-methyl-cyclohexane.

Uses of 2-Methylcyclohexanol: it is used to produce acetic acid-(2-methyl-cyclohexyl ester) by reaction with acetic acid anhydride. The reaction occurs with reagent chlorotrimethylsilane and solvent acetonitrile for 2 hours. The yield is about 91 %.

2-Methylcyclohexanol is used to produce acetic acid-(2-methyl-cyclohexyl ester) by reaction with acetic acid anhydride.

You can still convert the following datas into molecular structure:
1. Canonical SMILES: CC1CCCCC1O
2. InChI: InChI=1S/C7H14O/c1-6-4-2-3-5-7(6)8/h6-8H,2-5H2,1H3
3. InChIKey: NDVWOBYBJYUSMF-UHFFFAOYSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intramuscular 1gm/kg (1000mg/kg)   Journal of Scientific and Industrial Research, Section C: Biological Sciences. Vol. 21, Pg. 342, 1962.

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