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2-ethylisothiourea

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Identification
Molecular formula
C4H10N2S
CAS number
583-81-9
IUPAC name
2-ethylisothiourea
State
State

At room temperature, 2-ethylisothiourea is in a solid state, appearing as crystalline powder.

Melting point (Celsius)
119.50
Melting point (Kelvin)
392.70
Boiling point (Celsius)
273.15
Boiling point (Kelvin)
546.30
General information
Molecular weight
117.19g/mol
Molar mass
117.1940g/mol
Density
1.0100g/cm3
Appearence

2-Ethylisothiourea typically appears as a white or off-white crystalline solid.

Comment on solubility

Solubility of 2-ethylisothiourea

2-ethylisothiourea (C4H10N2S) is an intriguing compound with notable solubility characteristics. Understanding its solubility is crucial for various applications in chemical research and industry.

Key Solubility Insights:

  • Water Solubility: 2-ethylisothiourea is generally soluble in water, making it versatile for biochemical applications.
  • Solvent Compatibility: It shows good solubility in polar organic solvents such as methanol and ethanol, enhancing its accessibility in different chemical environments.
  • Solubility Influences: The solubility may be affected by factors such as temperature and pH, which can modify the interactions between the solute and solvent molecules.

Due to its high polarity and functional groups, 2-ethylisothiourea tends to interact favorably with water and other polar solvents, making it a significant compound for those studying chemical reactivity and synthesis. As we delve deeper into solubility dynamics, it is essential to remember that these characteristics play a pivotal role in the compound's applications.

Interesting facts

Interesting Facts about 2-ethylisothiourea

2-ethylisothiourea is a fascinating compound known for its unique structure and versatile applications in the field of chemistry. Here are some key points to consider:

  • Chemical Structure: This compound features a thiourea functional group, which is characterized by the presence of a sulfur atom double-bonded to carbon and bonded to two amine groups. This structure contributes to its chemical reactivity and biological activity.
  • Biological Significance: 2-ethylisothiourea has been studied for its role as an inhibitor of various enzymes, particularly in the context of research on diseases such as cancer and diabetes. Its ability to influence biological pathways makes it a valuable compound for scientific investigations.
  • Research Applications: It's widely used as a chemical probe in pharmacological studies to better understand its effects on the central nervous system and other physiological processes. Researchers often explore its potential in drug development and therapeutic applications.
  • Versatility in Reactions: The thiourea functional group allows for a range of chemical reactions. It can undergo transformations such as nucleophilic substitutions and can be used as a building block for synthesizing more complex compounds.
  • Safety Considerations: While 2-ethylisothiourea is useful in laboratories, it is essential to handle it with care, as compounds containing sulfur can be toxic and should be used following appropriate safety procedures.

In summary, 2-ethylisothiourea is more than just a chemical compound; it serves as a crucial tool in both research and applications in medicinal chemistry, embodying the intersection of structural intrigue and functional utility. As the renowned chemist Linus Pauling once stated, "The best way to have a good idea is to have lots of ideas." 2-ethylisothiourea exemplifies this philosophy, inspiring further exploration and innovation in the realm of chemical science.

Synonyms
s-ethylisothiourea
etiron
ethyron
2-Ethyl-2-thiopseudourea
ethyl carbamimidothioate
2986-20-1
ETHYLISOTHIOUREA
2-Ethyl-isothiourea
Carbamimidothioic acid, ethyl ester
S-ethylisothiouronium
Pseudourea, 2-ethyl-2-thio-
236P47H4VR
(ethylsulfanyl)methanimidamide
S-EIT (hydrobromide)
CHEMBL321691
DTXSID50183973
S-Ethylisothiuronium bromide; S-Ethylthiuronium bromide; WR 539
EIT-hydrobromide
S-ethyl-thioureum
s-ethyl-iso-thiourea
Ethiron (Salt/Mix)
Ethyl imidothiocarbamate
Tocris-0873
ethylsulfanyl-formamidine
Lopac-E-3149
Ethyl imidothiocarbamate #
WR 539 (Salt/Mix)
Lopac0_000491
SCHEMBL160501
UNII-236P47H4VR
USAF EL-18 (Salt/Mix)
DTXCID90106464
BDBM50055281
HSCI1_000396
STK370557
AKOS005446218
CCG-204582
DB02234
SDCCGSBI-0050475.P002
Bromide S-ethylisothiuronium (Salt/Mix)
NCGC00015407-01
NCGC00015407-02
NCGC00015407-03
NCGC00015407-04
NCGC00015407-07
NCGC00024835-01
NCGC00024835-02
NS00015308
EN300-7275002
2-Ethyl-2-thiopseudourea hydrobromide (Salt/Mix)
AE-641/00560030
BRD-K81623406-004-03-4
BRD-K81623406-004-08-3
Q27096309
Pseudourea, 2-ethyl-2-thio-, hydrobromide (Salt/Mix)
Carbamimidothioic acid, ethyl ester, monohydrobromide (Salt/Mix)