Skip to main content

Acetaminonitrosomethyl-mercaptobutyric acid

ADVERTISEMENT
Identification
Molecular formula
C8H14N2O5S
CAS number
.
IUPAC name
2-acetamido-3-methyl-3-nitrososulfanyl-butanoic acid
State
State

At room temperature, this compound exists in a solid crystalline state.

Melting point (Celsius)
130.00
Melting point (Kelvin)
403.00
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.00
General information
Molecular weight
221.25g/mol
Molar mass
221.2450g/mol
Density
1.2000g/cm3
Appearence

The compound appears as a light-yellow crystalline powder due to the presence of a nitroso group, which commonly imparts a yellowish hue to chemical compounds. It may also appear slightly greenish, depending on the purity and specific crystalline form present.

Comment on solubility

Solubility of 2-acetamido-3-methyl-3-nitrososulfanyl-butanoic acid (C8H14N2O5S)

The solubility of 2-acetamido-3-methyl-3-nitrososulfanyl-butanoic acid is influenced by several factors related to its chemical structure and functional groups. Understanding these aspects can provide insights into its behavior in various solvents:

  • Polarity: The presence of the amide and nitroso functional groups contributes to the compound's polarity, which generally enhances solubility in polar solvents like water.
  • Hydrogen bonding: The carboxylic acid group can form hydrogen bonds, which further increases its solubility in polar environments.
  • Hydrophobicity: While the compound contains hydrophilic groups, the aromatic-like structure presents some hydrophobic characteristics, which could decrease solubility in non-polar solvents.
  • Temperature: Solubility often varies with temperature; for many compounds, increased temperature can lead to increased solubility in solvents.

In summary, while 2-acetamido-3-methyl-3-nitrososulfanyl-butanoic acid is likely to exhibit good solubility in polar solvents like water due to its polar functional groups, its overall solubility in non-polar solvents may be limited. As a rule of thumb, compounds with similar functional groups are generally more soluble in like solvents.

Interesting facts

Interesting Facts about 2-Acetamido-3-methyl-3-nitrososulfanyl-butanoic Acid

2-Acetamido-3-methyl-3-nitrososulfanyl-butanoic acid is a fascinating compound that belongs to the class of organic compounds known as amino acids. This compound is notable due to its unique structural features and potential applications in biochemical and pharmaceutical research. Here are some interesting points about this compound:

  • Biological Relevance: As an amino acid derivative, this compound may serve as a building block in protein synthesis, highlighting the importance of amino acids in biological processes.
  • Nitroso Group: The presence of a nitroso group (–NO) in its structure is particularly intriguing, as nitroso compounds are known for their *varied biological activities*, including potential roles in signaling and as bioactive agents.
  • Sulfanyl Functionality: The sulfanyl (-SH) functionality can impart distinctive chemical properties, such as reactivity towards electrophiles and its involvement in redox reactions. This feature may be leveraged in medicinal chemistry.
  • Potential Applications: Compounds like 2-acetamido-3-methyl-3-nitrososulfanyl-butanoic acid could be explored in drug design, targeting various diseases, thanks to their structural diversity and biological activity.
  • Research Focus: As researchers continue to explore nitroso compounds, this compound stands as a subject of interest for studies related to *oxidative stress and cellular signaling* pathways.

In conclusion, 2-acetamido-3-methyl-3-nitrososulfanyl-butanoic acid not only demonstrates the intricate interplay of structure and *functionality* in organic chemistry but also holds promise for further exploration in the realm of pharmaceuticals and biochemistry. As an ongoing area of study, the exploration of its reactivity and interactions could pave the way for innovative applications in science and medicine.

Synonyms
67776-06-1
snap
S-Nitroso-N-acetyl-DL-penicillamine
Valine,N-acetyl-3-(nitrosothio)-
S-Nitroso-N-acetyl-D,L-penicillamine
2-acetamido-3-methyl-3-(nitrososulfanyl)butanoic acid
SNAP (amino acid)
152971-80-7
N-Acetyl-S-nitroso-DL-penicillamine
DL-Valine, N-acetyl-3-(nitrosothio)-
2-Acetamido-3-methyl-3-nitrososulfanylbutanoic acid
(+/-)-S-Nitroso-N-acetylpenicillamine
C4AX527AX8
S-Nitroso-N-acetylpenicillamine
SNAP (S-NITROSO-N-ACETYLPENICILLAMINE)
MFCD00272624
N-Acetyl-3-(nitrosothio)-DL-valine
2-acetamido-3-methyl-3-nitrososulfanyl-butanoic acid
NSC312630
2-ACETAMIDO-3-METHYL-3-(NITROSOTHIO)BUTANOIC ACID
S-Nitroso-N-acetylpenicillamine, (+/-)
S-Nitrosoacetylpenicillamine
(R)-2-Acetamido-3-methyl-3-(nitrosothio)butanoic acid
Valine, N-acetyl-3-(nitrosothio)-
SNAP [S-Nitroso-N-acetylpenicillamine]
DTXSID80897531
NSC-312630
Spectrum_001453
SpecPlus_000805
Spectrum2_001466
Spectrum3_000773
Spectrum4_001043
Spectrum5_001916
UNII-C4AX527AX8
BSPBio_002446
KBioGR_001306
KBioSS_001933
CHEMBL27308
DivK1c_006901
SCHEMBL139789
SPECTRUM1502060
SPBio_001391
KBio1_001845
KBio2_001933
KBio2_004501
KBio2_007069
KBio3_001666
S-nitroso-N-Acetyl-penicillamine
DTXSID70987112
ZIIQCSMRQKCOCT-UHFFFAOYSA-N
HMS1923O15
SNAP (+/-)
BCP21207
SNAP (+/-)-
CCG-39274
HSCI1_000047
AKOS024458576
FS46817
N-ACETYL-3-(NITROSOTHIO)VALINE
SB13130
NCGC00015734-03
NCGC00015734-04
NCGC00024673-02
NCGC00024673-03
AS-60790
SY099074
SNAP;N-Acetyl-3-(nitrosothio)-DL-valine
HY-121526
CS-0082469
P19575
S-NITROSO-N-ACETYL-DL-PENICILLAMINE 98%
N-(1-Hydroxyethylidene)-3-(nitrososulfanyl)valine
S-NITROSO-N-ACETYLPENICILLAMINE, (+/-)-
SR-01000597612
SR-01000597612-1
S-Nitroso-N-acetyl-DL-penicillamine, >=97%, powder
2-Acetamido-3-methyl-3-(nitrososulfanyl)butanoic acid (Ac-DL-Pen(NO)-OH)
636-172-4