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Diallyl sulfide

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Identification
Molecular formula
C6H10S
CAS number
592-88-1
IUPAC name
3-allylsulfanylprop-1-ene
State
State

At room temperature, diallyl sulfide is in a liquid state.

Melting point (Celsius)
-84.00
Melting point (Kelvin)
189.15
Boiling point (Celsius)
139.00
Boiling point (Kelvin)
412.15
General information
Molecular weight
114.21g/mol
Molar mass
114.2070g/mol
Density
0.9260g/cm3
Appearence

Diallyl sulfide is a clear, pale-yellow liquid with a strong garlic-like odor. It is notable for its characteristic sharp and pungent smell reminiscent of garlic.

Comment on solubility

Solubility of 3-allylsulfanylprop-1-ene

3-allylsulfanylprop-1-ene, a compound with both sulfur and hydrocarbon components, exhibits interesting solubility characteristics that are influenced by its molecular structure.

This compound generally shows moderate solubility in organic solvents due to its hydrocarbon chains, which enhance interactions with non-polar solvents. However, it is typically insoluble in water because of the lack of polar functional groups that can interact with water molecules.

Key Points about Solubility:

  • Organic Solvents: Likely soluble in solvents like ethanol, acetone, and diethyl ether.
  • Water: Insoluble due to the non-polar nature of hydrocarbons outweighing the influence of the sulfanyl group.
  • Temperature Effects: Solubility may increase with temperature, which can reduce the solvent's viscosity and enhance solute-solvent interactions.

In summary, while 3-allylsulfanylprop-1-ene finds compatibility with various organic solvents, its solubility profile is indicative of a broader trend among many organic compounds: the balance between polar and non-polar characteristics is crucial in determining solubility.

Interesting facts

Interesting Facts about 3-allylsulfanylprop-1-ene

3-allylsulfanylprop-1-ene, a fascinating compound, possesses some unique characteristics that make it a subject of interest in chemical research. Here are some noteworthy points:

  • Functional Group Diversity: This compound features a sulfur atom bonded to an allyl group, which introduces reactivity that can be harnessed in synthetic pathways. The presence of sulfur in organic compounds can lead to interesting chemical behaviors due to its ability to participate in various types of reactions, such as nucleophilic substitutions and thiol chemistry.
  • Potential Applications: Compounds containing sulfur play important roles in the pharmaceutical industry. They can act as intermediates in the synthesis of biologically active molecules, particularly antibiotics and anticancer agents. The unique structure of 3-allylsulfanylprop-1-ene suggests its potential utility in drug development.
  • Role in Organic Synthesis: The double bond in the propene component can undergo various reactions, such as:
    • Addition reactions – where new atoms or groups can be added across the double bond.
    • Polymerization – enabling the formation of larger molecules from smaller units, which can lead to interesting materials with specific desirable properties.
  • Biochemical Significance: Sulfur-containing compounds are essential in biological systems. They can serve as cofactors or structural components in enzymes and proteins, which are crucial for numerous biological reactions.
  • Synthetic Strategies: Chemists can employ specific reaction conditions to manipulate the structure of 3-allylsulfanylprop-1-ene, allowing for the exploration of its derivatives. These derivatives can be invaluable in the search for novel molecules with specific activities.

In summary, 3-allylsulfanylprop-1-ene is not just another organic compound; it encapsulates the convergence of synthetic chemistry, biological significance, and the potential for innovative applications. As we delve deeper into the characteristics and reactions of such compounds, we can uncover new pathways toward technological advancements and therapeutic solutions.

Synonyms
DIALLYL SULFIDE
Allyl sulfide
592-88-1
Diallyl sulphide
Diallyl thioether
1-Propene, 3,3'-thiobis-
Diallyl monosulfide
Thioallyl ether
Allyl monosulfide
diallylsulfide
Allyl sulphide
2-Propenyl sulphide
3,3-Thiobis(1-propene)
3-prop-2-enylsulfanylprop-1-ene
FEMA No. 2042
NSC 20947
CCRIS 3252
3-Allylsulfanyl-propene
Di(2-propenyl) sulfide
HSDB 7333
Bis(2-propenyl) sulfide
EINECS 209-775-1
60G7CF7CWZ
diallyl monosulphide
BRN 1736016
AI3-18865
NSC-20947
ALLYL SULFIDE [MI]
ALLYL SULFIDE [FHFI]
ALLYL SULFIDE [HSDB]
3,3'-thiobis(prop-1-ene)
ALLYL SULFIDE [USP-RS]
DI(2-PROPENYL) SULPHIDE
BIS(2-PROPENYL) SULPHIDE
4-01-00-02097 (Beilstein Handbook Reference)
NSC20947
ALLYL SULFIDE (USP-RS)
2Propenyl sulphide
3,3"-Thiobispropane
Diallyl sulfide (DAS)
3,3'Thiobis(1propene)
3,3'-Thiobis-1-propene
209-775-1
inchi=1/c6h10s/c1-3-5-7-6-4-2/h3-4h,1-2,5-6h
3-(prop-2-en-1-ylsulfanyl)prop-1-ene
di-2-Propenyl sulfide
Dially monosulfide
MFCD00008658
CHEBI:4489
CHEMBL170458
3-allylsulfanylprop-1-ene
UNII-60G7CF7CWZ
Diallysulfide
Diallyl thioather
di-2-propenylsulfide
Allyl sulfide, 97%
Spectrum2_000837
Spectrum3_001991
1-Propene,3'-thiobis-
4-Thia-1,6-heptadiene
SCHEMBL45800
BSPBio_003591
Prop-1-ene-3,3'-thiobis
(CH2=CHCH2)2S
3-(Allylsulfanyl)-1-propene
SPECTRUM1505293
SPBio_000793
Allyl sulfide, >=97%, FG
WLN: 1U2S2U1
DTXSID6060470
3-(Allylsulfanyl)-1-propene #
FEMA 2042
KBio3_003027
3,3'-Thiobis-1-propene, 9CI
Allyl sulfide, analytical standard
AAA59288
BDBM50318452
CCG-40295
STL453662
AKOS015897442
SDCCGMLS-0066835.P001
NCGC00095345-01
NCGC00095345-02
LS-13159
DB-053358
A0235
NS00012208
C08370
EN300-220520
SR-05000002373
SR-05000002373-1
Q11587666
Z1208219429
Allyl sulfide, United States Pharmacopeia (USP) Reference Standard