What is the density of 4 Methylcyclohexanol?

What is the density of 4 Methylcyclohexanol?

0.917 g/mL

0.917 g/mL at 25 °C (lit.)

Is 4 Methylcyclohexanol a primary alcohol?

4-Methylcyclohexanemethanol (MCHM, systematic name 4-methylcyclohexylmethanol) is an organic compound with the formula CH3C6H10CH2OH. Classified as a saturated higher alicyclic primary alcohol.

Is 4 Methylcyclohexanol soluble in water?

Soluble in water (15mg/ml at 20°C),ether,alcohols,and many organic solvents.

What are the products of the dehydration reaction of 4 Methylcyclohexanol?

This week experiment, 4-methylcyclohexanol undergoes acid-catalyzed dehydration to give 4-methylcyclohexene. The product is distilled from the reaction flask along with water generated. Then, the distillate is washed with salt solution, dried and distilled.

Is 4 Methylcyclohexene flammable?

Combustible. Above 70°C explosive vapour/air mixtures may be formed. NO open flames.

What is the density of 2 Methylcyclohexanol?

2-Methylcyclohexanol

Common Name 2-Methylcyclohexanol
Density 0.9±0.1 g/cm3 Boiling Point
Molecular Formula C7H14O Melting Point
MSDS Chinese USA Flash Point
Symbol GHS07 Signal Word

What is 4 methylcyclohexene used for?

4-Methylcyclohexene is used in the synthesis of an enantiomerically pure oxaliplatin derivative, {(1R,2R,4R)-4-Methyl-1,2-cyclohexanediamine}oxalatoplatinum(II), which exhibits good anticancer activity. It is also used in the preparation of N,N-diethyldithiocarbamate functionalized 1,4-polyisoprenes.

Is 4 methylcyclohexene flammable?

Is 4 Methylcyclohexanol flammable?

What is the boiling point of 4 Methylcyclohexanol?

343.4°F (173°C)4-methylcyclohexanol / Boiling point

What is 4-Methylcyclohexene used for?

Is 4-Methylcyclohexene soluble in water?

For use in citrus compositions.

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Appearance: colorless clear liquid (est)
Soluble in:
alcohol
water, 45.39 mg/L @ 25 °C (est)

What is the density of 1 Methylcyclohexanol?

0.919 g/mL
0.919 g/mL at 25 °C (lit.)

Is 2-methylcyclohexanol flammable?

Flammable. Above 58°C explosive vapour/air mixtures may be formed. NO open flames, NO sparks and NO smoking.

What is Methylcyclohexanol used for?

Methyl Cyclohexanol is a straw-colored liquid with a weak coconut odor. It is used as a solvent and in making textiles, silk, and soap.

Is 2 Methylcyclohexanol toxic?

Harmful if inhaled. May cause eye, skin, and respiratory tract irritation.

What type of alcohol is 1-Methylcyclohexanol?

tertiary alcohol
1-Methylcyclohexanol is a tertiary alcohol.

Is 2-methylcyclohexanol solid or liquid?

COLOURLESS VISCOUS LIQUID
COLOURLESS VISCOUS LIQUID WITH CHARACTERISTIC ODOUR. Flash point: 58°C c.c. The substance can be absorbed into the body by inhalation of its vapour and by ingestion.

Is 2-methylcyclohexanol and alcohol?

Insoluble in water. 2-METHYLCYCLOHEXANOL is an alcohol. Flammable and/or toxic gases are generated by the combination of these materials with alkali metals, nitrides, and strong reducing agents.

Is 2-methylcyclohexanol toxic?

Is 2-methylcyclohexanol a secondary alcohol?

Thus, the goal of this work is to offer an interesting green approach for the reaction of alcohol dehydration using as, primary alcohols: 1-heptanol and 1-octanol; as secondary alcohols: cyclohexanol and 2-methylcyclohexanol, and as tertiary alcohol 1-methylcyclohexanol, using an activated bentonitic clay (Tonsil) as …

Is Methylcyclohexanol a secondary alcohol?

1-Methylcyclohexanol is a tertiary alcohol.

Is 2-methylcyclohexanol a tertiary alcohol?

Is dehydration of 2-methylcyclohexanol?

Overall Reaction: 2-methylcyclohexanol undergoes a dehydration reaction when reacted with conc. Sulfuric acid to give the two main products shown in the overall reaction below.

What is the purpose of dehydration of 2-methylcyclohexanol?

The dehydration of 2-methylcyclohexanol proceeds through an E1 elimination. The acid catalyst protonates the hydroxy group converting it into a good leaving group, a neutral molecule of water. The water departs on its own, generating a carbocation, which quickly eliminates a beta-proton to form a double bond.

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