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6-Methylhept-5-en-2-ol

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Identification
Molecular formula
C8H16O
CAS number
10482-56-1
IUPAC name
6-methylhept-5-en-2-ol
State
State
Liquid at room temperature with a characteristic aromatic odor. It is typically stored in airtight containers to prevent evaporation.
Melting point (Celsius)
-70.00
Melting point (Kelvin)
203.15
Boiling point (Celsius)
165.00
Boiling point (Kelvin)
438.15
General information
Molecular weight
128.21g/mol
Molar mass
128.2120g/mol
Density
0.8214g/cm3
Appearence

6-Methylhept-5-en-2-ol is a colorless liquid with a characteristic odor. It is often used in fragrance and flavoring applications due to its pleasant smell.

Comment on solubility

Solubility of 6-methylhept-5-en-2-ol

6-methylhept-5-en-2-ol, a tertiary alcohol, exhibits notable solubility characteristics primarily due to the presence of its hydroxyl functional group. Alcohols generally possess the ability to dissolve in both polar and non-polar solvents, thanks to their unique structure that contains both hydrophobic and hydrophilic regions. The solubility of this compound can be summarized as follows:

  • In water: While the hydroxyl group allows for hydrogen bonding with water molecules, the long hydrocarbon chain can limit its overall water solubility. It is expected to be *moderately soluble* in water.
  • In organic solvents: 6-methylhept-5-en-2-ol is likely to be highly soluble in non-polar organic solvents such as hexane or ether due to its hydrocarbon portions, which facilitate interactions with these solvent types.
  • Temperature Dependence: As with many organic compounds, an increase in temperature may enhance the solubility of 6-methylhept-5-en-2-ol in various solvents.

Overall, the solubility profile of 6-methylhept-5-en-2-ol highlights the interplay of its functional groups and molecular structure, making it an interesting subject in the study of solubility behavior in organic chemistry.

Interesting facts

Interesting Facts about 6-Methylhept-5-en-2-ol

6-Methylhept-5-en-2-ol is an intriguing organic compound that belongs to the class of alcohols. Its structure is characterized by a long carbon chain with both double bond and hydroxyl group, which lends it distinct chemical properties. Here are some compelling aspects of this compound:

  • Natural Occurrence: This compound is often found in essential oils and contributes to the aromatic profiles of certain plants, making it valuable in the field of flavor and fragrance.
  • Synthesis: Chemists can synthesize 6-methylhept-5-en-2-ol through various methods, including the use of alkylation reactions or by employing specific catalysts to promote the formation of the double bond while introducing the hydroxyl group.
  • Versatility: This compound's reactivity allows it to participate in a variety of chemical reactions, such as oxidation and esterification, expanding its utility in organic synthesis and industrial applications.
  • Research Implications: Due to its structural features, 6-methylhept-5-en-2-ol is a subject of interest in medicinal chemistry, where it may serve as a precursor for the development of new pharmaceutical substances.

The compound serves as a prime example of how organic molecules can be manipulated to create different functionalities. As stated by renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." Exploring compounds like 6-methylhept-5-en-2-ol unveils a multitude of potential pathways for innovation in diverse fields, from bioengineering to environmental chemistry.

In summary, 6-methylhept-5-en-2-ol not only highlights the complexity of organic compounds but also inspires ongoing research and development endeavors that could lead to groundbreaking discoveries.

Synonyms
6-METHYL-5-HEPTEN-2-OL
6-Methylhept-5-en-2-ol
Sulcatol
1569-60-4
5-Hepten-2-ol, 6-methyl-
2-Methyl-2-hepten-6-ol
6-Hydroxy-2-methyl-2-heptene
NSC 66273
DTXSID8051754
EINECS 216-377-1
NSC-66273
33321H09GI
AI3-25074
DTXCID7030309
FEMA NO. 4884
CHEBI:15833
(+-)-SULCATOL
(+-)-6-METHYL-5-HEPTEN-2-OL
216-377-1
(+/-)-6-Methyl-5-Hepten-2-ol
4630-06-2
(R)-Sulcatol
6-methyl-hept-5-en-2-ol
MFCD00004561
dl-6-Methyl-5-hepten-2-ol
(+/-)-SULCATOL
Heptenol,methyl-
UNII-33321H09GI
coriander heptenol
SCHEMBL195482
6-Methyl-5-hepten-2-ol, 99%
NSC66273
Tox21_303934
LMFA05000566
Sulcatol (6-Methylhept-5-en-2-ol)
AKOS008996527
SB45311
SB45412
(.+/-.)-6-Methyl-5-hepten-2-ol
NCGC00357173-01
AS-58307
6-Methyl-5-hepten-2-ol, >=99%, FG
CAS-1569-60-4
DB-064153
CS-0132739
CS-0356782
NS00012901
C07288
E81628
EN300-1259133
Q27098251