Interesting facts
Interesting Facts About 3-Aminopropyl(methyl)phosphinic Acid
3-Aminopropyl(methyl)phosphinic acid is a fascinating compound in the realm of organic phosphorus chemistry. Here are some key insights:
- Biological Significance: This compound plays a vital role in biochemical research. Its structural features make it an interesting candidate for studying enzyme activities and interactions at the molecular level.
- Applications: 3-Aminopropyl(methyl)phosphinic acid is often utilized in the formulation of pharmaceuticals and agrochemicals. Its unique properties may aid in the development of novel drugs with specific therapeutic targets.
- Synthesis: A variety of synthetic routes have been developed to obtain this phosphinic acid. These include methods employing classical organic synthesis techniques as well as more innovative approaches involving transition metal catalysis.
- Amine Functionality: The presence of both amino and phosphinic acid functional groups allows this compound to participate in various chemical reactions, enhancing its utility in organic synthesis.
- Research Potential: The compound is increasingly coming under investigation for its potential roles in treating neurological disorders, owing to its phosphonic acid moiety, which can mimic the action of neurotransmitters.
In summary, 3-aminopropyl(methyl)phosphinic acid is not only a significant research compound due to its diverse applications but also a synthetic challenge that excites chemists who are interested in the intersections of organic and medicinal chemistry.
Synonyms
127729-35-5
3-aminopropyl(methyl)phosphinic Acid
3-Apmpa
SKF 97541
skf-97541
SK&F 97541
CGP 35024
CGP35024
(3-aminopropyl)methylphosphinic acid
(3-aminopropyl)(methyl)phosphinic acid
(3-(Aminopropyl)methyl)phosphinic acid
Phosphinic acid, (3-aminopropyl)methyl-
SKF97541
Phosphinic acid, P-(3-aminopropyl)-P-methyl-
Phosphinic acid, (3-(aminopropyl)methyl)-
CHEMBL112710
DTXSID80925969
SKF 97541 hydrochloride
3-aminopropyl-methylphosphinic acid
(R)-(3-aminopropyl)methylphosphinic acid
SKF-97541;SKF97541;CGP 35024;CGP-35024;CGP35024
C4H12NO2P
SR-01000076225
QD7
CGP-35024
SKF-97,541
Tocris-0379
Lopac-A-196
Biomol-NT_000257
Lopac0_000098
SCHEMBL341867
BPBio1_001014
GTPL1080
BDBM24185
3-aminopropylmethylphosphinic acid
CHEBI:232376
DTXCID401354789
HB0954
PDSP1_001483
PDSP2_001467
STK538161
3-aminopropylphosphinic derivative, 2
AKOS005468710
AT41793
CCG-204193
SK F 97541
NCGC00015015-01
NCGC00015015-02
NCGC00015015-03
NCGC00015015-04
NCGC00015015-05
NCGC00024562-01
NCGC00024562-02
NCGC00024562-03
HY-100915
CS-0020585
L000069
Q7390605
SR-01000076225-3
802-793-6
Solubility of 3-aminopropyl(methyl)phosphinic acid
3-aminopropyl(methyl)phosphinic acid, with the chemical formula C4H12NO2P, exhibits notable solubility characteristics that are essential for its applications in various fields. The presence of both an amino group and a phosphinic acid moiety contributes to its solubility profile.
Key Factors Influencing Solubility:
It is often reported that, *"solubility in water aids the bioavailability of phosphinic compounds,"* and 3-aminopropyl(methyl)phosphinic acid is no exception. This characteristic allows it to be effectively utilized in biochemical applications where aqueous solubility is critical.
In summary, the solubility of 3-aminopropyl(methyl)phosphinic acid can be described as:
Understanding these solubility properties is essential for researchers and practitioners working with this compound.