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2-(1,3,4-Thiadiazol-2-yl)ethanamine

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Identification
Molecular formula
C4H7N3S
CAS number
2941-59-7
IUPAC name
2-(1,3,4-thiadiazol-2-yl)ethanamine
State
State

At room temperature, 2-(1,3,4-Thiadiazol-2-yl)ethanamine is generally in a solid crystalline state, exhibiting stability under standard conditions.

Melting point (Celsius)
61.00
Melting point (Kelvin)
334.15
Boiling point (Celsius)
214.00
Boiling point (Kelvin)
487.15
General information
Molecular weight
129.17g/mol
Molar mass
129.1710g/mol
Density
1.2620g/cm3
Appearence

2-(1,3,4-Thiadiazol-2-yl)ethanamine appears as a white to off-white crystalline solid. The compound is typically synthesized for specific chemical research applications and is mainly used in the scientific community.

Comment on solubility

Solubility Overview of 2-(1,3,4-thiadiazol-2-yl)ethanamine

The solubility of 2-(1,3,4-thiadiazol-2-yl)ethanamine (C4H7N3S) can be described as follows:

Key Factors Influencing Solubility:

  • Polarity: The presence of nitrogen and sulfur atoms contributes to the compound's polar nature, which often enhances its solubility in polar solvents.
  • Hydrogen Bonding: This compound can engage in hydrogen bonding due to its amine functionality, further influencing its solubility in water.
  • Solvent Interactions: It tends to dissolve better in solvents that can interact favorably with its heteroatoms.

In general, 2-(1,3,4-thiadiazol-2-yl)ethanamine exhibits moderate solubility in aqueous solutions, attributed primarily to its polar structure and the ability to form hydrogen bonds. However, its solubility may vary based on the specific conditions and the presence of other solubilizing agents.

Practical Implications:

Understanding the solubility of this compound is crucial for its applications in various chemical processes, including:

  • Drug formulation, where solubility directly impacts bioavailability.
  • Synthesis reactions, where solubility can affect the reaction rate and product yield.

In summary, the solubility behavior of 2-(1,3,4-thiadiazol-2-yl)ethanamine is a key factor in its applications within both industrial and laboratory settings.

Interesting facts

2-(1,3,4-Thiadiazol-2-yl)ethanamine: Fascinating Insights

2-(1,3,4-thiadiazol-2-yl)ethanamine is an intriguing compound notable for its diverse range of applications and significance in various fields. Here are some interesting facts about this compound:

  • Pharmaceutical Potential: Due to its unique thiadiazole structure, this compound is often explored in drug development. Thiadiazoles have shown potential antimicrobial, antifungal, and anticancer properties, making them valuable in pharmacology.
  • Synergistic Effects: Research suggests that the incorporation of the ethanamine group can enhance the activity of the thiadiazole framework, potentially leading to more effective therapeutic agents. This highlights the importance of structure-activity relationships in medicinal chemistry.
  • Applications in Agriculture: Compounds like 2-(1,3,4-thiadiazol-2-yl)ethanamine are also studied for their role in agriculture. Some derivatives may serve as fungicides or pesticides, helping to protect crops and increase yield.
  • Research and Development: This compound has sparked considerable interest in the scientific community, prompting numerous studies. Researchers are particularly focused on optimizing its synthesis and exploring its reactivity.
  • Possibility of Further Modifications: The presence of the amino group opens avenues for further modification, enabling the design of new derivatives with tailored properties for specific applications in science and technology.

Overall, 2-(1,3,4-thiadiazol-2-yl)ethanamine is a compound rich in potential, showcasing the incredible versatility of thiadiazole derivatives in both medicinal and agricultural chemistry. The ongoing exploration of its properties and applications exemplifies the exciting developments within the field.

Synonyms
1,3,4-THIADIAZOLE-2-ETHYLAMINE
1097305-12-8
2-(1,3,4-thiadiazol-2-yl)ethanamine
2-(1,3,4-THIADIAZOL-2-YL)ETHAN-1-AMINE
BRN 0110762
AI3-52466
1,3,4-THIADIAZOLE, 2-ETHYLAMINO-
SCHEMBL8628811
SCHEMBL9601983
SCHEMBL9601985
AKOS013476603
PB27207
CS-0057216
P12515
EN300-1663623