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Methyl cysteinate

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Identification
Molecular formula
C4H9NO2S
CAS number
2363-07-1
IUPAC name
methyl 2-amino-3-sulfanyl-propanoate
State
State

Methyl cysteinate is typically found in a solid state at room temperature.

Melting point (Celsius)
75.00
Melting point (Kelvin)
348.20
Boiling point (Celsius)
208.50
Boiling point (Kelvin)
481.60
General information
Molecular weight
151.19g/mol
Molar mass
151.1880g/mol
Density
1.1870g/cm3
Appearence

Methyl cysteinate is a white crystalline solid. It is characterized by its distinct crystal lattice that gives it a uniform appearance. The crystals may appear as fine, needle-like structures under magnification.

Comment on solubility

Solubility of Methyl 2-amino-3-sulfanyl-propanoate

Methyl 2-amino-3-sulfanyl-propanoate (C4H9NO2S) is a fascinating compound with distinct solubility characteristics. Understanding its solubility can provide insights into its behavior in various environments and applications.

Solubility Characteristics:

  • Polar Nature: Due to the presence of both an amino group (-NH2) and a sulfanyl group (-SH), methyl 2-amino-3-sulfanyl-propanoate exhibits a significant degree of polarity, which enhances its solubility in polar solvents.
  • Water Solubility: It is expected to be soluble in water due to hydrogen bonding capabilities provided by its amino and sulfanyl functionalities.
  • Organic Solvents: This compound can also dissolve in organic solvents, especially those that can interact through dipole-dipole interactions or hydrogen bonding.
  • Influence of pH: The solubility may vary with changes in pH, particularly because the amino group can accept a proton, potentially increasing solubility in more acidic conditions.

In summary, methyl 2-amino-3-sulfanyl-propanoate exhibits notable solubility in polar solvents, including water, which enhances its utility in biochemical applications. Its chemical structure allows it to function effectively across a variety of conditions, adding to its versatility in chemical use.

Interesting facts

Interesting Facts about Methyl 2-amino-3-sulfanyl-propanoate

Methyl 2-amino-3-sulfanyl-propanoate, also known as a derivative of the naturally occurring compound cysteine, encompasses a unique combination of functional groups that contribute to its interesting chemical properties. This compound belongs to the class of amino acids and serves as a building block for peptides and proteins.

Key Properties and Applications:

  • Biological Importance: Its structure provides crucial amino and sulfanyl groups that can participate in a variety of biochemical reactions, making it vital in biological systems.
  • Versatile Reactivity: This compound can act as a nucleophile due to the presence of the thiol (-SH) group, enabling it to participate in redox reactions and nucleophilic substitutions.
  • Potential Therapeutics: Methyl 2-amino-3-sulfanyl-propanoate is studied for its potential health benefits and therapeutic applications, particularly in anticancer and antioxidant activities, due to its ability to scavenge free radicals.
  • Flavor and Fragrance: Amino acids, especially sulfur-containing compounds, often are implicated in the development of flavors and fragrances in various food products.

A fascinating aspect of methyl 2-amino-3-sulfanyl-propanoate is its role in biological systems and how it can influence the health of living organisms. As scientists say, "Nature teaches us that even small molecules can have profound impacts." Whether through its biological activity or potential applications in organic synthesis, studying this compound opens up numerous possibilities for advancements in both chemistry and medicine.

The exploration of methyl 2-amino-3-sulfanyl-propanoate not only enhances our understanding of amino acid chemistry but also emphasizes the interconnectedness of various chemical structures in our everyday lives.

Synonyms
Methyl DL-cysteinate
44641-43-2
Methyl 2-amino-3-sulfanylpropanoate
methyl cysteinate
EINECS 256-161-4
cysteinmethylester
Spectrum_000586
Spectrum2_000014
Spectrum3_000273
Spectrum4_000399
Spectrum5_001545
SCHEMBL21034
BSPBio_001746
KBioGR_000957
KBioSS_001066
DivK1c_000071
SPBio_000047
CHEMBL1622757
KBio1_000071
KBio2_001066
KBio2_003634
KBio2_006202
KBio3_001246
DTXSID80859735
MCYHPZGUONZRGO-UHFFFAOYSA-N
NINDS_000071
Methyl2-amino-3-sulfanylpropanoate
STL301684
AKOS017268996
IDI1_000071
NCGC00179039-01
SBI-0051568.P002
EN300-34175
AB00053569_02
BRD-A77473570-003-04-2
Z56917374
methyl (2R)-2-amino-3-sulfanylpropanoate,hydrochloride
256-161-4