Interesting facts
Interesting Facts About 2-amino-3-(2-diazoacetyl)oxy-propanoic Acid
2-amino-3-(2-diazoacetyl)oxy-propanoic acid, often simply referred to by its systematic name, is a distinctive compound with several implications in both synthetic chemistry and biological sciences. Here are some of the remarkable aspects of this compound:
- Structure and Functionality: The compound contains both amino and diazo functional groups, making it a versatile molecule for various chemical reactions. Its unique structure allows it to participate in cross-linking reactions that are pivotal in polymer chemistry.
- Biological Relevance: Due to its amino acid nature, it can be considered for applications in biochemistry. It may be involved in metabolic pathways and have potential uses in drug design, particularly in targeting specific biomolecules.
- Diazo Compounds: The presence of the diazo group (–N=N–) provides this compound with interesting photochemical properties, enabling it to undergo photoinduced reactions which can be exploited for light-activated processes in organic synthesis.
- Scientific Research: Researchers are exploring the potential of compounds like 2-amino-3-(2-diazoacetyl)oxy-propanoic acid in the field of materials science, specifically in developing new materials with tailored properties for various applications.
- Novel Derivatives: This compound serves as a platform for the development of novel derivatives through reactivity modification. By altering the functional groups, scientists can create personalized molecules for specific applications in medicinal chemistry.
In conclusion, 2-amino-3-(2-diazoacetyl)oxy-propanoic acid is not just another chemical compound; it is a gateway to exploring new realms of chemical reactivity and biological significance. The ongoing research around it poses fascinating opportunities for advancements in both synthetic methodologies and therapeutic avenues.
Synonyms
D-Azaserine
NSC166613
NCGC00018164-02
O-Diazoacethylserin
76749-44-5
CI-337;O-Diazoacetyl-L-serine;P-165
Spectrum_002000
Spectrum2_001221
Spectrum3_001853
Spectrum4_001258
SCHEMBL8862
BSPBio_003266
KBioGR_001816
KBioSS_002576
DivK1c_000319
SPECTRUM1502113
SPBio_001062
CHEMBL1651884
BDBM39339
cid_5284344
HMS500P21
KBio1_000319
KBio2_002567
KBio2_005135
KBio2_007703
KBio3_002767
NINDS_000319
HMS1923O17
HMS2092D12
HMS3371A15
Pharmakon1600-01502113
CCG-39932
NSC758188
NSC-166613
NSC-758188
IDI1_000319
NCGC00018164-03
NCGC00018164-04
NCGC00095279-01
NCGC00095279-02
NCGC00095279-03
NS00011809
F85193
AB00053161_02
SR-05000001597
SR-05000001597-1
BRD-A67065070-001-04-7
(E)-1-[(2S)-2-amino-2-carboxy-ethoxy]-2-diazonio-ethenolate
(E)-1-[(2S)-2-amino-2-carboxyethoxy]-2-diazonioethenolate
aminoacid antagonist: inhibits protein and nucleic acid synthesis
(E)-1-[(2S)-2-azanyl-3-oxidanyl-3-oxidanylidene-propoxy]-2-diazonio-ethenolate
Solubility of 2-amino-3-(2-diazoacetyl)oxy-propanoic acid (C5H5N3O4)
The solubility of 2-amino-3-(2-diazoacetyl)oxy-propanoic acid is a topic of interest due to its functional groups and molecular structure. Generally, its solubility can be assessed in various solvents, with the following key points to consider:
To sum up, the solubility behavior of 2-amino-3-(2-diazoacetyl)oxy-propanoic acid is shaped by its chemical structure and the surrounding environment, making it essential to consider these factors when exploring its dissolution characteristics. Understanding these solubility properties is crucial for its applications in chemical and biological contexts.