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Sabinene

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Identification
Molecular formula
C10H16
CAS number
3387-41-5
IUPAC name
3,7,7-trimethylbicyclo[4.1.0]hept-3-ene
State
State

At room temperature, sabinene is typically found in a liquid state.

Melting point (Celsius)
-51.80
Melting point (Kelvin)
221.35
Boiling point (Celsius)
163.00
Boiling point (Kelvin)
436.15
General information
Molecular weight
136.24g/mol
Molar mass
136.2380g/mol
Density
0.8475g/cm3
Appearence

Sabinene is a colorless liquid with a mild, pleasant, and somewhat spicy odor.

Comment on solubility

Solubility of 3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene

The solubility of 3,7,7-trimethylbicyclo[4.1.0]hept-3-ene can be characterized by its structural properties and polar interactions in various solvents. Here are several key points regarding its solubility:

  • Non-polar Nature: This compound is predominantly non-polar due to the presence of multiple methyl groups and the bicyclic structure, leading to limited solubility in polar solvents such as water.
  • Solvent Compatibility: It demonstrates greater solubility in non-polar organic solvents. Possible solvents include:
    • Hexane
    • Chloroform
    • Petroleum ether
  • Temperature Effects: Like many organic compounds, solubility generally increases with temperature. However, this trend may vary based on the solvent used.
  • Applications: Understanding its solubility is crucial for processing and application in fields such as organic synthesis and materials science.

In summary, the solubility of 3,7,7-trimethylbicyclo[4.1.0]hept-3-ene is predominantly non-polar, making it suitable for use in non-polar solvents. Its unique structure plays a significant role in determining its interaction with different solvent types.

Interesting facts

Interesting Facts about 3,7,7-trimethylbicyclo[4.1.0]hept-3-ene

3,7,7-trimethylbicyclo[4.1.0]hept-3-ene is a fascinating compound that exemplifies the complexity and beauty of organic chemistry. Here are some intriguing aspects of this unique bicyclic structure:

  • Bicyclic Structure: This compound features a bicyclic framework, consisting of two interconnected rings. Specifically, it contains a seven-membered ring fused to another smaller ring, resulting in its distinct chemical properties.
  • Unique Isomerism: As a bicyclic compound, it exhibits geometric and stereoisomerism, leading to various possible configurations. This diversity in arrangements makes it a subject of interest for researchers studying isomeric behavior and reactivity.
  • Source of Natural Compounds: Compounds with similar structures are often found in natural products, particularly in essential oils and plant metabolites. This highlights the compound's relevance in fields like pharmacognosy and natural product chemistry.
  • Applications in Synthesis: 3,7,7-trimethylbicyclo[4.1.0]hept-3-ene serves as a valuable building block in organic synthesis, facilitating the creation of more complex molecules, potentially useful in pharmaceuticals and materials science.
  • Curiosity in Research: The study of this compound can yield insights into reaction mechanisms and the effects of strain in bicyclic systems. As researchers explore its properties, they may uncover new applications or reactivity patterns that could lead to exciting innovations.

In conclusion, 3,7,7-trimethylbicyclo[4.1.0]hept-3-ene stands as a testament to the richness of organic chemistry. Its structural characteristics, potential applications, and the challenges it presents in terms of reactivity make it a compelling subject for further study within the scientific community.

Synonyms
3-Carene
13466-78-9
3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene
Delta-3-Carene
DELTA3-Carene
Bicyclo[4.1.0]hept-3-ene, 3,7,7-trimethyl-
Delta(3)-Carene
DTXSID4047462
3,7,7-Trimethylbicyclo(4.1.0)hept-3-ene
DTXCID2027462
Bicyclo(4.1.0)hept-3-ene, 3,7,7-trimethyl-
FEMA NO. 3821
236-719-3
3-Karen
3-Norcarene, 3,7,7-trimethyl-
H2M15SNR6N
S-3-Carene
Carene
Car-3-ene
Delta-car-3-ene
MFCD00001315
(+-)-delta3-Carene
(+-)-3-Carene
74806-04-5
CHEBI:35661
(1S)-(+)-3-Carene
Bicyclo(4.1.0)hept-3-ene, 3,7,7(or 4,7,7)-trimethyl-
3,7,7-Trimethylbicyclo[4.1.0]-3-heptene
3,7,7-trimethyl-bicyclo[4.1.0]hept-3-ene
Bicyclo[4.1.0]hept-3-ene, 3,7,7(or 4,7,7)-trimethyl-
(+)Car-3-ene
.delta. 3-carene
3-.delta.-Carene
.DELTA.-caR-3-ene
4,7,7-Trimethyl-3-norcarene
alpha-Carene
3,7,7-trimethyl bicyclohept-3-ene
4,7,7-trimethylbicyclo[4.1.0]hept-3-ene
3-delta-Carene
carene (delta-3-)
?-3-Carene
3,7,7(or 4,7,7)-Trimethylbicyclo(4.1.0)hept-3-ene
delta-3-Carene (GC)
3-Carene, 90%
3-Carene, >=90%
3-Carene, analytical standard
SCHEMBL112444
CHEMBL506854
orb1710576
HY-N6663
Tox21_302632
s5595
SBB060476
AKOS015840953
CCG-266136
NCGC00256842-01
AS-80902
FD159271
CAS-13466-78-9
DB-063033
CS-0083202
NS00001492
ST51046655
E77192
EN300-173315
Bicyclo[4.1.0]hept-3-ene, 3,7,7-trimethyl-, (1R,6S)-rel-