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(1,5-dimethyl-1-vinyl-hex-4-enyl) 2-methylpropanoate

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Identification
Molecular formula
C15H26O2
CAS number
25134-09-2
IUPAC name
(1,5-dimethyl-1-vinyl-hex-4-enyl) 2-methylpropanoate
State
State

At room temperature, (1,5-dimethyl-1-vinyl-hex-4-enyl) 2-methylpropanoate is in liquid state.

Melting point (Celsius)
-40.00
Melting point (Kelvin)
233.15
Boiling point (Celsius)
240.00
Boiling point (Kelvin)
513.15
General information
Molecular weight
226.37g/mol
Molar mass
226.3740g/mol
Density
0.8705g/cm3
Appearence

(1,5-Dimethyl-1-vinyl-hex-4-enyl) 2-methylpropanoate appears as a colorless liquid. It has a faint, characteristic odor that is often reminiscent of fruity notes, making it common in the fragrance and flavor industry.

Comment on solubility

Solubility Characteristics of (1,5-dimethyl-1-vinyl-hex-4-enyl) 2-methylpropanoate

The solubility of (1,5-dimethyl-1-vinyl-hex-4-enyl) 2-methylpropanoate is influenced by its molecular structure, which consists of both hydrocarbon and ester functional groups. This combination leads to interesting solubility behaviors in different solvents.

Key Factors Affecting Solubility:

  • Polarity: The ester group tends to increase solubility in polar solvents compared to non-polar solvents. However, the bulky hydrocarbon sections may hinder this interaction.
  • Chain Length: The length of the hydrocarbon chains can affect the overall solubility. Longer chains may reduce solubility in water due to increased hydrophobic character.
  • Temperature: Like many organic compounds, solubility generally increases with temperature, allowing for greater dissolution of the compound in solvents.

In practical scenarios, you might find that (1,5-dimethyl-1-vinyl-hex-4-enyl) 2-methylpropanoate exhibits higher solubility in organic solvents such as ethanol, acetone, and chloroform, while its solubility in water is likely to be limited. Always consider the specific application or usage when evaluating its solubility profile.

Interesting facts

Interesting Facts about (1,5-Dimethyl-1-vinyl-hex-4-enyl) 2-methylpropanoate

(1,5-Dimethyl-1-vinyl-hex-4-enyl) 2-methylpropanoate is a fascinating compound that showcases the complexity and richness of organic chemistry. Here are some intriguing aspects to consider:

  • Functional Groups: This compound contains both an ester and multiple vinyl groups, which can impart unique reactivity characteristics. The presence of vinyl groups often suggests opportunities for polymerization reactions, making this compound of particular interest in materials science.
  • Synthetic Applications: The structure indicates potential for synthesis in creating advanced materials, such as polymers or additives in surfactants. In addition, esters like this one are commonly used in the fragrance and flavor industry due to their pleasant aromas.
  • Biological Relevance: Compounds similar to this one may be studied for their biological activity, including antimicrobial or anticancer properties. The complexity of its structure can lead to unique interactions with biological systems.
  • Isomerism: The presence of multiple chiral centers may result in various stereoisomers. Understanding their different properties and behaviors would be a key area of exploration in structural organic chemistry.
  • Environmental Impact: Like many organic compounds, studies on its environmental degradation and effects on ecosystems are crucial. Chemists aim to design compounds that are not only effective in their intended applications but also environmentally friendly.

In conclusion, the intricate nature of (1,5-Dimethyl-1-vinyl-hex-4-enyl) 2-methylpropanoate offers a wealth of study opportunities. The intersection of synthetic utility, biological activity, and environmental considerations makes this compound a topic worthy of exploration in both academic and industrial chemistry.

Synonyms
Linalyl isobutyrate
78-35-3
Linalool isobutyrate
Linalyl 2-methylpropanoate
Isobutyric acid, linalyl ester
Linalool, isobutyrate
3,7-dimethylocta-1,6-dien-3-yl 2-methylpropanoate
FEMA No. 2640
1,5-Dimethyl-1-vinyl-4-hexenyl isobutyrate
3,7-Dimethyl-1,6-octadienyl isobutyrate
1,6-Octadien-3-ol, 3,7-dimethyl-, isobutyrate
NSC 46145
3,7-Dimethyl-1,6-octadien-3-yl isobutyrate
ISOBUTYRIC ACID, 1,5-DIMETHYL-1-VINYL-4-HEXENYL ESTER
1,5-Dimethyl-1-vinylhex-4-enyl isobutyrate
EINECS 201-108-2
EINECS 305-132-5
3,7-Dimethyl-1,6-octadien-3-ol isobutyrate
3,7-Dimethyl-1,6-octadien-3-yl isobutanoate
BRN 1726378
DTXSID6047490
3,7-Dimethyl-1,6-octadien-3-yl 2-methylpropanoate
1-Ethenyl-1,5-dimethyl-4-hexenyl 2-methylpropanoate
AI3-24264
Propanoic acid, 2-methyl-, 1-ethenyl-1,5-dimethyl-4-hexenyl ester
NSC-46145
(1)-1,5-Dimethyl-1-vinylhex-4-enyl isobutyrate
8867Y4G46L
Isobutyric acid, linalyl ester (6CI)
DTXCID4027490
LINALYL ISOBUTYRATE [FCC]
LINALYL ISOBUTYRATE [FHFI]
4-02-00-00849 (Beilstein Handbook Reference)
Propanoic acid, 2-methyl-, 1-ethenyl-1,5-dimethyl-4-hexen-1-yl ester
3,7-Dimethylocta-1,6-dien-3-yl isobutyrate
1,5-Dimethyl-1-vinyl-4-hexenyl 2-methylpropanoate
linalylisobutyrat
UNII-8867Y4G46L
Linalol isobutyrate
Linalyl iso-Butyrate
3,6-octadienyl isobutyrate
SCHEMBL560781
3,6-octadien-3-yl isobutyrate
CHEMBL3185164
FEMA 2640
1, 3,7-dimethyl-, isobutyrate
CHEBI:171776
NSC46145
Tox21_302721
AKOS015837556
CAS-78-35-3
NCGC00256753-01
AS-77518
3,7-Dimethyl-1, 6-octadienyl isobutyrate
WLN: 1Y1&VOX1&1U1&3UY1&1
DB-056304
NS00012795
3, 7-Dimethyl-1,6-octadien-3-yl isobutyrate
D93228
Isobutyric acid,5-dimethyl-1-vinyl-4-hexenyl ester
Q27269894
Propanoic acid, 1-ethenyl-1,5-dimethyl-4-hexenyl ester