2,4,6-Trimethyl-1,3,5-trithiane | Solubility of Things

Identification

Molecular formula

C₆H₁₂S₃

CAS number

1002-43-3

IUPAC name

2,4,6-trimethyl-1,3,5-trithiane

State

At room temperature, 2,4,6-trimethyl-1,3,5-trithiane exists as a solid. It is stable under standard conditions but may emit sulfurous odor upon decomposition or when heated intensely.

Melting point (Celsius)

45.50

Melting point (Kelvin)

318.70

Boiling point (Celsius)

220.50

Boiling point (Kelvin)

493.70

General information

Molecular weight

178.36g/mol

Molar mass

178.3610g/mol

Density

1.1489g/cm³

Appearence

2,4,6-Trimethyl-1,3,5-trithiane is typically a colorless solid. It tends to form crystalline structures and may appear as crystalline powder or small crystals. Its specific appearance, such as crystal size and shape, can depend on the crystallization conditions.

Comment on solubility

Solubility of 2,4,6-trimethyl-1,3,5-trithiane

2,4,6-trimethyl-1,3,5-trithiane is a sulfur-containing organic compound known for its unique structure and characteristics. When considering its solubility, several factors come into play:

Solvent Compatibility: This compound exhibits moderate solubility in polar solvents such as water, due to its sulfur atoms which can engage in dipole-dipole interactions.
Hydrophobic Nature: The presence of multiple methyl groups contributes to its hydrophobic character, which may hinder solubility in highly polar solvents.
Complexation: The sulfur atoms can participate in forming complexes, potentially enhancing solubility in certain organic solvents.
Temperature Dependency: It is widely recognized that temperature plays a critical role in solubility; increasing temperature generally improves the solubility of organic compounds.

As a summary, while ^C₇^H₁₄^S₃ compound may show varied solubility based on solvent choice and environmental conditions, it remains a fascinating subject of study for its properties and potential applications.

Interesting facts

Interesting Facts about 2,4,6-trimethyl-1,3,5-trithiane

2,4,6-trimethyl-1,3,5-trithiane is a fascinating compound, primarily recognized for its intriguing structure and unique properties. Here are several interesting aspects worth noting:

Structure: This compound features a trithiane ring, which is characterized by sulfur atoms within a six-membered ring. The inclusion of three methyl groups at positions 2, 4, and 6 contributes to its distinctive chemical behavior and reactivity.
Synthesis: The synthesis of 2,4,6-trimethyl-1,3,5-trithiane can typically be achieved through the reaction of 1,3,5-trithiolanes with various methylating agents. This pathway showcases the versatility in organic synthesis, enriching the repertoire of thioether chemistry.
Applications: Beyond its theoretical interest, this compound finds application as a sulfur source in various organic synthesis reactions. It also serves as a precursor for the production of more complex compounds, particularly in materials science and pharmaceuticals.
Oxidative Stability: 2,4,6-trimethyl-1,3,5-trithiane exhibits notable stability under oxidative conditions compared to other sulfur-containing compounds, making it an intriguing subject for studies related to oxidation processes.
Smell: The distinct sulfur chemistry often imparts a characteristic odor to thioethers. While the exact scent of 2,4,6-trimethyl-1,3,5-trithiane may vary, sulfur compounds are generally known for their pungent, often unpleasant aromas, which can be a notable point of discussion in labs.
Research Interest: Ongoing research into thioethers like this compound continues to reveal novel applications in catalysis, organic reactions, and materials development, showcasing the compound's significance in advancing chemical science.

The study of 2,4,6-trimethyl-1,3,5-trithiane brings together the marvels of organic chemistry and the practical implications of sulfur-containing compounds, making it an engaging topic for both students and seasoned researchers.

Synonyms

2,4,6-TRIMETHYL-1,3,5-TRITHIANE

Trithioacetaldehyde

2765-04-0

Thioacetaldehyde trimer

1,3,5-Trithiane, 2,4,6-trimethyl-

2,4,6-Trimethyl-s-trithiane

s-Trithiane, 2,4,6-trimethyl-

UNII-C6MG282Q6S

Thioacetaldehyde cyclic trimer

1,3,5-Trimethyl-S-trithiane

1,3,5-Trimethyl-2,4,6-trithiane

C6MG282Q6S

DTXSID20863018

NSC 227897

NSC-227897

DTXCID90811703

668-690-1

inchi=1/c6h12s3/c1-4-7-5(2)9-6(3)8-4/h4-6h,1-3h

xqvyldfspbxacs-uhfffaoysa-n

23769-39-3

alpha-Trithioacetaldehyde

beta-Trithioacetaldehyde

K8GLL4NEZI

(2alpha,4alpha,6alpha)-2,4,6-Trimethyl-1,3,5-trithiane

cis-2,4,6-Trimethyl-1,3,5-trithiane

4HQ3RWP831

cis,cis-2,4,6-Trimethyl-1,3,5-trithiane

23769-40-6

S-Trithiane, 2,4,6-trimethyl-, cis-2,4,cis-2,6-

1,3,5-Trithiane, 2,4,6-trimethyl, #1

1,3,5-Trithiane, 2,4,6-trimethyl, #2

TRANS-2,4,6-TRIMETHYL-1,3,5-TRITHIANE

UNII-K8GLL4NEZI

UNII-4HQ3RWP831

Thioacetaldehyde beta-form [MI]

EINECS 245-870-4

beta-2,4,6-Trimethyl-1,3,5-trithiane

1,5-Trimethyl-s-trithiane

2,6-Trimethyl-s-trithiane

s-Trithiane,4,6-trimethyl-

SCHEMBL1641407

.BETA.-TRITHIOACETALDEHYDE

CHEBI:169269

.ALPHA.-TRITHIOACETALDEHYDE

2,6-Trimethyl-1,3,5-trithiane

DTXSID901030914

1,3,5-Trithiane, 2,4,6-trimethyl-, (2alpha,4alpha,6alpha)-

2E,6E-Trimethyl-1,3,5-trithiane

NSC227897

1,5-Trithiane, 2,4,6-trimethyl-

AKOS024337231

2E,4E,6E-Trimethyl-1,3,5-trithiane

2E, 4E,6E-Trimethyl-1,3,5-trithiane

THIOACETALDEHYDE .BETA.-FORM [MI]

DB-239485

NS00051634

NS00126699

THIOACETALDEHYDE .ALPHA.- FORM [MI]

.ALPHA.-2,4,6-TRIMETHYL-1,3,5-TRITHIANE

.BETA.-2,4,6-TRIMETHYL-1,3,5-TRITHIANE

2,4,6-Trimethyl-S-trithiane (trithioacetaldehyde)

Q27259604

Q27282085

1,3,5-TRITHIANE, 2,4,6-TRIMETHYL-, (2.ALPHA.,4.ALPHA.,6.ALPHA.)-

1,3,5-TRITHIANE, 2,4,6-TRIMETHYL-, (2.ALPHA.,4.ALPHA.,6.BETA.)-