Interesting facts
Interesting Facts about 2-Methylisothiourea
2-Methylisothiourea is a unique compound that has captured the attention of chemists and biologists alike due to its intriguing properties and applications. Here are some noteworthy points:
- Biological Relevance: This compound is often utilized in biological studies, especially in research related to nitric oxide synthase and other enzymatic activities. Its ability to inhibit certain reactions makes it a valuable tool in understanding biochemical pathways.
- Synthesis and Reactivity: The synthesis of 2-methylisothiourea involves reacting isothiourea with methylating agents, showcasing the importance of functional groups in organic synthesis.
Furthermore, its reactivity allows it to participate in diverse chemical reactions, leading to the formation of various derivatives. - Structural Characteristics: The presence of the thiourea functional group plays a crucial role in the compound's properties. The molecular framework contributes to its diverse biological activities, particularly as a potential modulator for neurotransmitter systems.
- Safety and Handling: While working with 2-methylisothiourea, proper safety measures should be taken. It is advised to handle the compound in a fume hood and wear appropriate personal protective equipment, as with many chemical substances.
In summary, 2-methylisothiourea exemplifies the exciting intersection of organic chemistry and biological research, making it a compound of interest for ongoing studies and applications. Its unique properties not only enhance our understanding of biochemical processes but also pave the way for potential future therapeutic applications.
Synonyms
methyl carbamimidothioate
s-methylisothiourea
2986-19-8
2-methylisothiourea
Carbamimidothioic acid, methyl ester
S-Methyl isothiourea
S-Methyl-isothiourea
S-Methylisothiouronium
S-methylthiourea
2-methyl-2-thiopseudourea
S-Methylisothiopseudouronium
S-Methylisothiourea sulfate
S-Methylthiopseudouronium iodide
2-Methyl-isothiourea
S-methylpseudothiourea
UNII-ES8C3884JW
carbamimidothioic acid methyl ester
CHEMBL356703
ES8C3884JW
S-Methyl-ITU
S-Methylthiuronium sulfate
methylisothiuronium
2-Methylisothio urea
SR-01000075165
1068-58-2
2-Methyl-2-thiopseudourea hemisulfate salt
2-methyl-2-pseudothiourea
pseudourea, 2-methyl-2-thio-
MFCD00129752
S-methylthiopseudourea
Methyl imidothiocarbamate
Z2-S-methyl isothiourea
SMT
Lopac-M-3127
Methyl imidothiocarbamate #
Lopac0_000755
DTXSID60903780
BBL013049
BDBM50055282
HSCI1_000214
STK301762
AKOS003291597
AKOS016371841
((amino(imino)methyl)-sulfanyl)methane
SDCCGSBI-0050733.P002
NCGC00015664-01
NCGC00015664-02
NCGC00015664-03
NCGC00015664-07
NCGC00162238-01
PS-17819
{[AMINO(IMINO)METHYL]SULFANYL}METHANE
CS-0179522
SR-01000075165-1
SR-01000075165-3
Q27277336
Solubility of 2-methylisothiourea
2-methylisothiourea (C2H7N3S) is a fascinating compound with significant solubility characteristics that can vary depending on the solvent used. Its solubility profile can be summarized as follows:
When discussing solubility, it is important to remember that the interactions between the solute and solvent play a crucial role in determining the overall solubility. According to the principle of like dissolves like, the polarity of the solvent used will significantly impact how well 2-methylisothiourea can be dissolved.
In summary, while 2-methylisothiourea exhibits good solubility in water, factors such as temperature, solvent choice, and pH are essential in understanding its overall solubility behavior. This highlights the importance of considering various conditions when working with this compound in laboratory settings.