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Sesamol

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Identification
Molecular formula
C7H6O3
CAS number
533-31-3
IUPAC name
1,3-benzodioxol-5-ylmethanol
State
State

Sesamol is typically a solid at room temperature, appearing as white crystals.

Melting point (Celsius)
64.00
Melting point (Kelvin)
337.15
Boiling point (Celsius)
327.60
Boiling point (Kelvin)
600.75
General information
Molecular weight
138.12g/mol
Molar mass
138.1220g/mol
Density
1.2890g/cm3
Appearence

Sesamol is a white crystalline solid.

Comment on solubility

Solubility of 1,3-benzodioxol-5-ylmethanol

1,3-benzodioxol-5-ylmethanol, a compound known for its unique structure, exhibits distinct solubility characteristics. Understanding its solubility provides vital insights into its potential applications in various fields. Here are some key points regarding its solubility:

  • Solvent Interaction: This compound is generally soluble in polar organic solvents such as methanol, ethanol, and acetone.
  • Water Solubility: It exhibits limited solubility in water, which can impact its usability in aqueous environments.
  • Temperature Dependence: As with many organic compounds, solubility can increase with temperature; therefore, conducting solubility tests at varying temperatures is advisable.
  • pH Effect: The solubility may also change with pH alterations; acid-base reactions can influence the solubility of functional groups in the compound.

Research indicates that "the solubility of a compound is a critical factor influencing its bioavailability and reactivity." Thus, knowing the solubility properties of 1,3-benzodioxol-5-ylmethanol is essential for chemists and researchers working with this intriguing compound.

Interesting facts

Interesting Facts about 1,3-Benzodioxol-5-ylmethanol

1,3-Benzodioxol-5-ylmethanol is a fascinating compound that draws attention for its unique structure and potential applications in various fields. Known for its presence in certain natural and synthetic compounds, it embodies a combination of aromatic and aliphatic characteristics, making it a subject of interest for chemists and researchers alike.

Chemical Structure

  • Aromatic Systems: The compound contains a benzodioxole structure, characterized by its two oxygen atoms creating a dioxole ring fused with a benzene ring.
  • Functional Groups: The presence of a hydroxymethyl group (–CH₂OH) enhances its reactivity and hydrophilicity, enabling diverse chemical behavior.

Biological Relevance

This compound serves as a key intermediate in various chemical syntheses, particularly in the production of:

  • Pharmaceuticals: Compounds similar to 1,3-benzodioxol-5-ylmethanol may exhibit interesting biological activities, including potential antioxidant and anti-inflammatory effects.
  • Flavor and Fragrance: Due to its aromatic profile, derivatives of this structure are often explored for use in cosmetics and food flavoring.

Applications in Research

Many researchers employ 1,3-benzodioxol-5-ylmethanol in the following ways:

  • Synthetic Organic Chemistry: Used as a building block for various organic reactions.
  • Material Science: Investigated for its potential as a precursor in synthesizing more complex polymeric materials.

In conclusion, 1,3-benzodioxol-5-ylmethanol is not just an ordinary compound; its intriguing structure and versatility open numerous avenues for exploration in chemistry and materials science. With ongoing research, the full potential of this compound continues to unfold, making it a compelling topic for chemical scientists and enthusiasts alike.

Synonyms
Piperonyl alcohol
495-76-1
Piperonol
1,3-BENZODIOXOLE-5-METHANOL
3,4-Methylenedioxybenzyl alcohol
Heliotropyl alcohol
5-Hydroxymethyl-1,3-benzodioxole
1-Hydroxymethyl-3,4-methylenedioxybenzene
NSC 26265
Benzyl alcohol, 3,4-(methylenedioxy)-
3,4-(Methylenedioxy)benzenemethanol
EINECS 207-808-4
NSC-26265
4163K563GS
AI3-05702
3,4-methylenedioxyphenylmethanol
Benzo[1,3]dioxol-5-ylmethanol
DTXSID3060089
HSDB 8494
(BENZODIOXOL-5-YL)METHANOL
BENZO(1,3)DIOXOL-5-YLMETHANOL
1,3Benzodioxole5methanol
5Hydroxymethyl1,3benzodioxole
DTXCID3040693
3,4(Methylenedioxy)benzyl alcohol
Benzyl alcohol, 3,4(methylenedioxy)
1Hydroxymethyl3,4methylenedioxybenzene
207-808-4
inchi=1/c8h8o3/c9-4-6-1-2-7-8(3-6)11-5-10-7/h1-3,9h,4-5h
1,3-Benzodioxol-5-ylmethanol
Benzo[d][1,3]dioxol-5-ylmethanol
5-(Hydroxymethyl)-1,3-benzodioxole
Benzo[1,3]dioxol-5-yl-methanol
3,4-(Methylenedioxy)phenylmethanol
3,4-(Methylenedioxy)benzyl alcohol
MFCD00005836
Helioalcohol
Piperonylalkohol
UNII-4163K563GS
(1,3-Benzodioxol-5-yl)methanol
A1BDV
Piperonyl alcohol, 98%
SCHEMBL49914
3,4-methylendioxybenzylalcohol
1,3-benzodioxol-5-yl-methanol
3,4-methylendioxy-benzylalcohol
(1,3-dioxaindan-5-yl)methanol
benz[1,3]dioxol-5-yl-methanol
DAlc2-H_000040
3,4 -methylendioxy-benzylalcohol
3,4-methylenedioxyphenyl methanol
3,4-methylenedioxy benzyl alcohol
3,4-methylenedioxy-benzyl alcohol
CHEBI:167431
Benzyl alcohol,4-(methylenedioxy)-
NSC26265
3,4-(methylenedioxy)-benzyl alcohol
BBL011934
STK397489
(2H-1,3-benzodioxol-5-yl)methanol
AKOS000119342
FP03936
FS-1186
SDCCGMLS-0065920.P001
SY033132
DB-051647
CS-0072132
NS00022238
P0457
EN300-20232
AP-065/40214405
Q27258401
F0001-1287
Z104477372