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4-Methyl-2-(2-methylprop-1-enyl)tetrahydropyran

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Identification
Molecular formula
C10H18O
CAS number
16409-42-8
IUPAC name
4-methyl-2-(2-methylprop-1-enyl)tetrahydropyran
State
State

At room temperature, 4-Methyl-2-(2-methylprop-1-enyl)tetrahydropyran is a liquid. Its relatively low melting point means it remains in this state under standard atmospheric conditions.

Melting point (Celsius)
-24.00
Melting point (Kelvin)
249.15
Boiling point (Celsius)
218.00
Boiling point (Kelvin)
491.15
General information
Molecular weight
154.25g/mol
Molar mass
154.2510g/mol
Density
0.8760g/cm3
Appearence

4-Methyl-2-(2-methylprop-1-enyl)tetrahydropyran typically appears as a colorless to pale yellow liquid. The compound may exhibit a characteristic, pleasant odor often described as fruity or citrus-like.

Comment on solubility

Solubility of 4-methyl-2-(2-methylprop-1-enyl)tetrahydropyran

When it comes to the solubility of 4-methyl-2-(2-methylprop-1-enyl)tetrahydropyran, we find a compound that displays distinct behavior based on its molecular structure. Here are some key points to consider:

  • Solvent Dependence: This compound is likely to be soluble in organic solvents due to its hydrophobic hydrocarbon chain and cyclic structure.
  • Polarity Influence: The presence of the tetrahydropyran ring suggests a degree of polarity. As a result, it may exhibit limited solubility in polar solvents like water.
  • Concentration Matters: The solubility can vary significantly with concentration. At higher concentrations, solubility **may decrease** due to the interactions between molecules.
  • Temperature Effects: Generally, an increase in temperature can enhance solubility in organic solvents, making it an important factor to consider when experimenting.

In summary, while 4-methyl-2-(2-methylprop-1-enyl)tetrahydropyran demonstrates some solubility in organic solvents, its behavior in polar solvents is limited. The specifics of solubility must always be investigated in the context of solvent choice, temperature, and concentration to fully understand its properties.

Interesting facts

Exploring 4-Methyl-2-(2-methylprop-1-enyl)tetrahydropyran

4-Methyl-2-(2-methylprop-1-enyl)tetrahydropyran is a fascinating organic compound that belongs to the class of tetrahydropyrans, which are saturated cyclic ethers. This specific structure is noteworthy for several reasons:

  • Diverse Applications: The compound holds potential in various fields, including medicinal chemistry and materials science, due to its unique structural characteristics.
  • Synthetic Versatility: Being a bicyclic compound, it offers valuable intermediates in organic synthesis, allowing chemists to create a range of complex molecules.
  • Structural Stability: The tetrahydropyran ring provides a stable framework, enabling it to resist hydrolysis and other chemical reactions, making it a useful building block.

In terms of its biological significance, compounds like 4-methyl-2-(2-methylprop-1-enyl)tetrahydropyran can often be found in natural products or serve as mimics for biologically active molecules. This raises intriguing questions among chemists, such as:

  • How might small modifications to its structure enhance its biological activity?
  • What novel reactions can be developed using this compound as a starting material?

Quotes from established chemists emphasize the importance of such compounds: "The chemistry of complexity begins with simple structures like tetrahydropyrans. They are the building blocks of life's intricate molecular tapestry." This highlights the role 4-methyl-2-(2-methylprop-1-enyl)tetrahydropyran may play in future research, echoing the sentiment among scientists that understanding these compounds is crucial for innovation.

In conclusion, 4-methyl-2-(2-methylprop-1-enyl)tetrahydropyran is not just a compound; it is a window into the vast possibilities of organic chemistry, inviting researchers to further explore its potential.

Synonyms
16409-43-1
Rose oxide
4-Methyl-2-(2-methylprop-1-en-1-yl)tetrahydro-2H-pyran
Rosenoxide
Rosoxide
4-methyl-2-(2-methylprop-1-enyl)oxane
FEMA No. 3236
Tetrahydro-4-methyl-2-(2-methyl-1-propenyl)-2H-pyran
2H-Pyran, tetrahydro-4-methyl-2-(2-methyl-1-propenyl)-
DTXSID1051771
Pyran, tetrahydro-4-methyl-2-(2-methylpropenyl)-
2H-Pyran, tetrahydro-4-methyl-2-(2-methylpropenyl)-
4-Methyl-2-(2-methyl-1-propenyl)tetrahydro-2H-pyran
Tetrahydro-4-methyl-2-(2-methylpropen-1-yl)pyran
4-methyl-2-(2-methylprop-1-en-1-yl)oxane
DTXCID0030326
CHEBI:90075
2-Isobutenyl-4-methyltetrahydropyran
4O51437J50
Tetrahydro-4-methyl-2-[2-methyl-1-propenyl]-2H-pyran
rose-oxide
240-457-5
2H-Pyran, tetrahydro-4-methyl-2-(2-methyl-1-propen-1-yl)-
MFCD00036607
4-methyl-2-(2-methylpropenyl)tetrahydro-2h-pyran
Fema 3236
Tetrahydro-4-methyl-2-(2-methylprop-1-enyl)pyran
Pyran, 2-(2-methyl-1-propenyl)-4-methyltetrahydro-
PYRAN, TETRAHYDRO-2-(2-METHYL-1-PROPENYL)-4-METHYL-
Rose oxide L
(Z)-Rose oxide
EINECS 240-457-5
BRN 0111348
Rosenoxid
rose_oxide
Rose oxide levo
cis Rose oxide
Rose oxide cis
laevo-rose oxide
UNII-4O51437J50
4-methyl-2-(2-methylprop-1-enyl)tetrahydropyran
Rose oxide , I
Tetrahydro-4-methyl-2-(2-methylpropenyl)-2H-pyran
5-17-01-00256 (Beilstein Handbook Reference)
SCHEMBL583714
isobutenyl methyltetrahydropyran
(4S)-2-(2-Methyl-1-propenyl)-4-methyltetrahydropyran
Tox21_303917
(+)-Rose oxide, analytical standard
(-)-Rose oxide, analytical standard
MSK014369
STL562853
AKOS006230485
NCGC00357165-01
DS-16478
SY052080
CAS-16409-43-1
DB-064521
CS-0155167
M2363
NS00013183
D91592
EN300-296303
4-Methyl-2-(2-methyl-1-propenyl)tetrahydropyran
Q417155
Tetrahydro-4-methyl-2-(2-methyl-1-propenyl)pyran, 9CI
4-Methyl-2-(2-methyl-1-propen-1-yl)tetrahydro-2H-pyran
Rose oxide 4-Methyl-2-(2-methyl-1-propenyl)-tetrahydropyran