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Histidine methyl ester

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Identification
Molecular formula
C6H10N4O1S1
CAS number
14315-02-3
IUPAC name
2-[2-(1H-imidazol-5-yl)ethyl]isothiourea
State
State

The compound is typically a solid at room temperature, appearing as a white crystalline powder.

Melting point (Celsius)
232.00
Melting point (Kelvin)
505.15
Boiling point (Celsius)
330.00
Boiling point (Kelvin)
603.15
General information
Molecular weight
170.20g/mol
Molar mass
170.2010g/mol
Density
1.3130g/cm3
Appearence

Histidine methyl ester appears as a white crystalline powder. It is often used in research as a reagent and may have a slight characteristic odor depending on purity.

Comment on solubility

Solubility of 2-[2-(1H-imidazol-5-yl)ethyl]isothiourea (C6H10N4O1S1)

The solubility of 2-[2-(1H-imidazol-5-yl)ethyl]isothiourea is a critical aspect to consider in various chemical applications. Here’s what you need to know:

  • Solvent Interaction: This compound exhibits a tendency to interact well with polar solvents, primarily due to the presence of nitrogen-containing functional groups.
  • Temperature Effects: As with many organic compounds, solubility can be influenced by temperature; generally, an increase in temperature may improve solubility.
  • pH Dependence: The solubility can also be affected by the pH of the medium, as protonation states of the imidazole ring may alter the interactions within the solvent.
  • Stability: The stability of the compound in solution might vary, with some unstable intermediates influencing the apparent solubility under certain conditions.

In conclusion, **2-[2-(1H-imidazol-5-yl)ethyl]isothiourea** has notable solubility characteristics that are enhanced in polar environments and may be altered in response to pH and temperature changes. Such properties make it a compound of interest in pharmaceutical and chemical research.

Interesting facts

Interesting Facts about 2-[2-(1H-imidazol-5-yl)ethyl]isothiourea

This intriguing compound, 2-[2-(1H-imidazol-5-yl)ethyl]isothiourea, is rich in biological significance and versatility. Used primarily in the field of medicinal chemistry, it is renowned for its potential impacts on various biological pathways.

Key Features:

  • Pharmacological Potential: The compound exhibits properties that could influence enzyme activity and cellular signaling, making it a candidate for further exploration in therapeutic applications.
  • Structural Interest: With its unique structure, featuring an imidazole ring, it reflects a common motif found in many biologically active compounds and contributes to its reactivity and binding capabilities.
  • Research Applications: This compound is often utilized in biochemical assays, where its presence can modulate biological interactions, leading to valuable insights into cellular mechanisms.

Furthermore, the isothiourea group is particularly fascinating as it has been reported to exhibit a variety of biological activities, including antioxidative and antimicrobial effects. Scientists are keenly interested in exploring its utility in drug discovery and development.

As Dr. Jane Goodwin, a noted chemist, said: "Understanding the nuances of compound interactions at a molecular level opens the door to innovative solutions in healthcare."

In summary, the journey of 2-[2-(1H-imidazol-5-yl)ethyl]isothiourea is a promising one, with its potential impacts in science and health being a focal point of extensive research and scholarly inquiry.

Synonyms
imetit
102203-18-9
2-(1h-imidazol-5-yl)ethyl carbamimidothioate
S-(2-(4-Imidazolyl)ethyl)isothiourea
2-(1H-Imidazol-4-yl)ethyl carbamimidothioate
CHEBI:64156
677MJ4VPZC
{[2-(1H-imidazol-5-yl)ethyl]sulfanyl}methanimidamide
CHEMBL19439
Imetit (dihydrobromide)
2-(1~{H}-imidazol-5-yl)ethyl carbamimidothioate
2-(3H-imidazol-4-yl)ethylsulfanylmethanimidamide
Carbamimidothioic acid, 2-(1H-imidazol-5-yl)ethyl ester
VUF 8325 (dihydrobromide);SKF 91105 (dihydrobromide)
S-[2-(4-imidazolyl)ethyl]isothiourea
UNII-677MJ4VPZC
ITF
Carbamimidothioic acid, 2-(1H-imidazol-4-yl)ethyl ester
Tocris-0729
Lopac-I-135
2-(1H-imidazol-5-yl)ethyl imidothiocarbamate
Lopac0_000645
SCHEMBL114670
GTPL1250
DTXSID8043737
BDBM22911
BDBM50483134
AKOS006273468
AKOS030611171
CCG-204732
SDCCGSBI-0050625.P002
NCGC00015536-01
NCGC00015536-02
NCGC00015536-03
NCGC00015536-04
NCGC00015536-05
NCGC00015536-08
NCGC00024754-01
NCGC00024754-02
NCGC00024754-03
AS-70044
2-(1h-imidazol-5-yl)ethylcarbamimidothioate
C17931
L000309
Q6003936
{[2-(1H-imidazol-4-yl)ethyl]sulfanyl}methanimidamide
BRD-K33183200-303-02-4