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Methionylalanine

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Identification
Molecular formula
C8H15N2O3S
CAS number
62957-45-5
IUPAC name
2-[(2-formamido-4-methylsulfanyl-butanoyl)amino]propanoic acid
State
State

At room temperature, methionylalanine is typically in a solid state. It is relatively stable and does not exhibit any volatility.

Melting point (Celsius)
310.00
Melting point (Kelvin)
583.15
Boiling point (Celsius)
228.00
Boiling point (Kelvin)
501.15
General information
Molecular weight
177.25g/mol
Molar mass
177.2460g/mol
Density
1.3100g/cm3
Appearence

Methionylalanine usually appears as a white solid crystalline powder. The appearance can vary slightly depending on the purity and form, but it generally maintains a similar solid state under room conditions.

Comment on solubility

Solubility of 2-[(2-formamido-4-methylsulfanyl-butanoyl)amino]propanoic acid

The solubility of 2-[(2-formamido-4-methylsulfanyl-butanoyl)amino]propanoic acid (C8H15N2O3S) can be influenced by several factors, including its functional groups and molecular structure. This compound contains both polar and non-polar characteristics, which can result in varying solubility profiles depending on the solvent used:

  • Polar solvents: Due to the presence of functional groups such as amides and carboxylic acids, the compound is expected to have good solubility in polar solvents like water and alcohols.
  • Non-polar solvents: The non-polar character introduced by the methylsulfanyl group may lead to reduced solubility in non-polar solvents.
  • pH dependence: As a carboxylic acid, its solubility may also vary with pH, showing increased solubility in basic conditions where it may ionize.

In summary, while 2-[(2-formamido-4-methylsulfanyl-butanoyl)amino]propanoic acid exhibits favorable solubility characteristics in polar environments, its behavior in non-polar solvents may not be as pronounced. Understanding the solubility behavior is crucial for applications in biological and chemical systems, especially for drug formulation and delivery.

Interesting facts

Interesting Facts about 2-[(2-formamido-4-methylsulfanyl-butanoyl)amino]propanoic acid

This compound, with a rather complex name, is an intriguing example of the *interplay between organic chemistry and biochemical functionality*. Here are some fascinating aspects worth exploring:

  • Bioactivity: Due to its structure, which incorporates amino acids and a sulfanyl group, it may exhibit significant biological activity. Compounds of this nature can serve as precursors for various bioactive molecules.
  • Synthetic Pathways: Organic synthesis strategies that lead to the formation of this compound can involve multiple reaction steps, particularly in assembling the amino acid backbone and introducing the sulfanyl moiety. These pathways are a testament to the *creativity and precision required in organic synthesis*.
  • Potential Applications: Exploring compounds like this one could open doors in fields such as pharmacology or agriculture, where derivatives might be utilized as therapeutic agents or bioactive pesticides, respectively.
  • Structural Complexity: The intricate arrangement of functional groups within this compound might also influence its interaction with enzymes or receptors, making it an interesting subject for *structure-activity relationship (SAR) studies*.

To quote the famous chemist Linus Pauling: "The best way to have a good idea is to have lots of ideas." This principle resonates strongly within the realm of chemical research, as the exploration of complex compounds like 2-[(2-formamido-4-methylsulfanyl-butanoyl)amino]propanoic acid can yield valuable insights into new scientific territories.

As we delve deeper into understanding such compounds, it is essential to appreciate not only their individual properties but also their *potential to contribute to advancing science and technology*.

Synonyms
N-Formyl-Met-Ala
N-formylmethionylalanine
KBio2_004238
Spectrum_001190
Spectrum2_001060
Spectrum3_001519
Spectrum4_000055
Spectrum5_001229
BSPBio_003197
KBioGR_000549
KBioSS_001670
MLS002207228
DivK1c_000925
SPBio_001020
SCHEMBL4287202
CHEMBL2130597
CHEBI:91785
HMS502O07
KBio1_000925
KBio2_001670
KBio2_006806
KBio3_002697
DTXSID10274432
NINDS_000925
CCG-40124
IDI1_000925
NCGC00178212-01
SMR001306773
DS-017338
Q27163587
2-[[2-formamido-4-(methylthio)-1-oxobutyl]amino]propanoic acid