CAS 767-12-4
:3,3-Dimethylcyclohexanol
Description:
3,3-Dimethylcyclohexanol is a cyclic alcohol characterized by its six-membered carbon ring structure with two methyl groups attached to the same carbon atom, specifically at the 3-position. This compound is a colorless to pale yellow liquid at room temperature and possesses a distinct, pleasant odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic cyclohexane ring. The presence of the hydroxyl (-OH) group imparts moderate polarity, influencing its reactivity and interactions. 3,3-Dimethylcyclohexanol can undergo typical alcohol reactions, including dehydration to form alkenes and oxidation to yield ketones or aldehydes. Its chemical structure allows for various stereoisomers, which can exhibit different physical and chemical properties. This compound is utilized in organic synthesis and as an intermediate in the production of fragrances and other chemical products. Safety data indicates that it should be handled with care, as it may cause irritation upon contact with skin or eyes.
Formula:C8H16O
InChI:InChI=1S/C8H16O/c1-8(2)5-3-4-7(9)6-8/h7,9H,3-6H2,1-2H3
InChI key:InChIKey=DQBDGNSFXSCBJX-UHFFFAOYSA-N
SMILES:CC1(C)CC(O)CCC1
Synonyms:- cyclohexanol, 3,3-dimethyl-
- 3,3-Dimethylcyclohexanol
- 3,3-Dimethylcyclohexan-1-ol
- Cyclohexanol, 3,3-dimethyl-
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Found 4 products.
Cyclohexanol,3,3-dimethyl-
CAS:Formula:C8H16OPurity:96%Color and Shape:LiquidMolecular weight:128.21203,3-Dimethylcyclohexan-1-ol
CAS:<p>Dimedone is a ketone that is found in the oils of many plants. It can be synthesized by the transformation of 3,3-dimethylcyclohexan-1-ol with ethynylation and sequence. This reaction sequence has been shown to produce high yields of dimedone.</p>Formula:C8H16OPurity:Min. 95%Molecular weight:128.21 g/mol
