Safrole | Solubility of Things

Identification

Molecular formula

C₁₀H₁₀O₂

CAS number

94-59-7

IUPAC name

6-allyl-4-methoxy-1,3-benzodioxole

State

At room temperature, safrole is a liquid.

Melting point (Celsius)

12.00

Melting point (Kelvin)

285.15

Boiling point (Celsius)

234.00

Boiling point (Kelvin)

507.15

General information

Molecular weight

162.19g/mol

Molar mass

162.1890g/mol

Density

1.0955g/cm³

Appearence

Safrole is a colorless to pale yellow oily liquid with a characteristic sweet, spicy odor reminiscent of sassafras. It exhibits a refractive index of about 1.540-1.542 and can solidify to form needle-like crystals at lower temperatures.

Comment on solubility

Solubility of 6-allyl-4-methoxy-1,3-benzodioxole

The solubility of 6-allyl-4-methoxy-1,3-benzodioxole (C₁₀H₁₀O₂) is a topic of interest due to its unique structure and potential applications in various fields. Here are some key points regarding its solubility:

Polarity: The compound contains both aromatic and methoxy groups, along with dioxole, which suggests a level of polarity that can influence solubility.
Solvent Compatibility: Based on its structure, 6-allyl-4-methoxy-1,3-benzodioxole is likely soluble in organic solvents such as ethanol and ether, but may have limited solubility in water.
Temperature Dependence: Like many organic compounds, its solubility might increase with temperature, leading to greater dissolution in non-polar or slightly polar solvents.
Structural Interactions: Intermolecular forces, such as hydrogen bonding and van der Waals interactions, can play a significant role in solubility behavior.

In summary, while specific solubility data may not be widely available for 6-allyl-4-methoxy-1,3-benzodioxole, understanding its chemical characteristics can provide valuable insights into its solubility potential. As always, experimental verification is recommended for precise applications.

Interesting facts

Exploring 6-Allyl-4-methoxy-1,3-benzodioxole

6-Allyl-4-methoxy-1,3-benzodioxole, a fascinating chemical compound, belongs to a class of organic compounds known for their distinctive aromatic properties. This compound features a unique benzodioxole structure, which is characterized by a fused dioxole ring, contributing to its interesting chemical behavior.

Key Characteristics

Aromatic Nature: The presence of the benzene ring provides significant stability and contributes to various chemical reactions, making it a versatile compound in organic chemistry.
Allyl Group: The allyl group attached to the structure enhances the reactivity, allowing for potential applications in synthetic organic chemistry.
4-Methoxy Substitution: The methoxy group acts as an electron-donating group, which can influence the compound's chemical reactivity and stability.

Applications and Significance

This compound holds promise in various fields, including:

Pharmaceutical Development: Compounds with similar structures are being investigated for their potential therapeutic effects, making them candidates in drug design.
Natural Products: Benzodioxole derivatives are often found in nature, linked to various biological activities, which can inspire novel therapeutic approaches.
Industrial Uses: Its chemical properties may offer potential applications in the synthesis of polymers and other materials.

Fun Fact

Drawing from the ancient idea that "the structure of a compound influences its behavior," scientists continue to explore how modified structures like that of 6-allyl-4-methoxy-1,3-benzodioxole can lead to novel discoveries and advancements in chemistry.

In summary, 6-allyl-4-methoxy-1,3-benzodioxole not only exemplifies the beauty and complexity of organic compounds but also opens doors to a multitude of possibilities in scientific research and application.

Synonyms

Myristicin

607-91-0

Myristicine

6-Allyl-4-methoxy-1,3-benzodioxole

Myristicin (6CI)

5-Allyl-1-methoxy-2,3-(methylenedioxy)benzene

4-Methoxy-6-(2-propenyl)-1,3-benzodioxole

CCRIS 6782

1,3-Benzodioxole, 4-methoxy-6-(2-propenyl)-

HSDB 3516

Benzene, 5-allyl-1-methoxy-2,3-(methylenedioxy)-

EINECS 210-146-9

5-Allyl-2,3-(methylendioxy)anisole

BRN 0166218

04PD6CT78W

DTXSID1025693

CHEBI:68234

MYRISTICIN [MI]

MFCD00133549

MYRISTICIN [HSDB]

6-allyl-4-methoxybenzo[d][1,3]dioxole

4-methoxy-6-(prop-2-en-1-yl)-2H-1,3-benzodioxole

DTXCID605693

4-Methoxy-6-[2-propenyl]-1,3-benzodioxole

5-19-02-00631 (Beilstein Handbook Reference)

1-Allyl-3-methoxy-4,5-methylenedioxybenzene

5-Allyl-1-methoxy-2,3-(methylenedioxy)-Benzene

4-Methoxy-6-(2-propenyl)-1,3-benzodioxole, 9CI

1-Methoxy-2,3-methylenedioxy-5-(2-propenyl)benzene

5-ALLYL-1-METHOXY-2,3-METHYLENEDIOXYBENZENE

UNII-04PD6CT78W

Myristicin_major

4-methoxy-6-prop-2-enyl-1,3-benzodioxole

Myristicin (Standard)

SCHEMBL68041

MLS001065535

6Allyl4methoxy1,3benzodioxole

Myristicin, analytical standard

CHEMBL481044

HY-N2510R

HMS2270K14

HY-N2510

Tox21_200172

4Methoxy6(2propenyl)1,3benzodioxole

BDBM50242966

s3291

STK693140

6-allyl-4-methoxy-benzo-1,3-dioxole

AKOS005604763

CCG-208543

FM26113

1,3Benzodioxole, 4methoxy6(2propenyl)

5Allyl1methoxy2,3(methylenedioxy)benzene

NCGC00091427-01

NCGC00091427-02

NCGC00257726-01

1ST40367

AC-34678

CAS-607-91-0

DA-75834

MS-23038

SMR000112534

Benzene, 5allyl1methoxy2,3(methylenedioxy)

CS-0022781

NS00017756

C10480

4-methoxy-6-(prop-2-en-1-yl)-1,3-benzodioxole

Q414057

SR-01000838340

6-ALLYL-1,3-BENZODIOXOL-4-YL METHYL ETHER

SR-01000838340-3

1,3-Benzodioxole, 4-methoxy-6-(2-propenyl)-(9CI)

1,3-Benzodioxole, 4-methoxy-6-(2-propenyl)- (9CI)

210-146-9

4-Methoxy-6-(2-propenyl)-1,3-benzodioxole;6-Allyl-4-methoxy-1,3-benzodioxole;5-Allyl-1-methoxy-2,3-(methylenedioxy)benzene