Interesting facts
Interesting Facts about 2-(Hydroxymethyl)-1-methyl-piperidine-3,4,5-triol
2-(Hydroxymethyl)-1-methyl-piperidine-3,4,5-triol is a fascinating chemical compound with several noteworthy characteristics, making it significant in both research and practical applications. Here are some interesting points to consider:
- Structural Diversity: This compound belongs to a class of piperidine derivatives, which are known for their diverse biological activities. Its unique structure includes a piperidine ring with three hydroxyl groups, showcasing its ability to participate in various chemical interactions.
- Biological Relevance: Compounds containing piperidine rings have been found to exhibit a range of pharmacological properties. This particular compound may have potential implications in medicinal chemistry, especially in the development of new therapeutic agents.
- Hydroxymethyl Functionality: The presence of hydroxymethyl groups in the compound provides interesting reactivity patterns, which can be exploited in further chemical synthesis or modification processes.
- Potential Applications: Research into similar compounds has indicated that they could be utilized in areas such as drug design, agrochemicals, or as biochemical probes in studies of enzyme activity.
- Synthetic Pathways: Understanding the synthesis of this compound can lead to insights into organic synthesis techniques and the methodologies employed to create complex molecules in the laboratory.
As scientists explore the properties and applications of 2-(hydroxymethyl)-1-methyl-piperidine-3,4,5-triol, they are likely to uncover even more intriguing characteristics and uses. The ongoing study of such compounds not only enriches our understanding of chemistry but also contributes to advancements in related fields.
Synonyms
N-Methyl-1-deoxynojirimycin
2-(hydroxymethyl)-1-methylpiperidine-3,4,5-triol
CHEMBL418746
3,4,5-Piperidinetriol,2-(hydroxymethyl)-1-methyl-, (2R,3R,4R,5S)-
MeDNJ
N-Methyl-DNJ
NMDNJ
N-Methyldesoxynojirimycin
1,5-Dideoxy-1,5-imino-1-methyl-D-sorbitol
CHEBI:166564
1,5-Dideoxy-1,5-(methylimino)-D-glucitol, 9CI
MOR 14;N-Methyl-1-deoxynojirimycin;N-Methylmoranolin
Lopac0_000773
2-(Hydroxymethyl)-1-methyl-3,4,5-piperidinetriol
SCHEMBL11159128
AAKDPDFZMNYDLR-UHFFFAOYSA-N
HMS3261I17
Tox21_500368
BDBM50076963
AKOS030240812
CCG-204858
LP00368
SDCCGSBI-0050751.P002
NCGC00015651-02
NCGC00261053-01
1,5-dideoxy-1,5-(methylimino)-d-glucitol
M 1777
2-Hydroxymethyl-1-methyl-piperidine-3,4,5-triol
SR-01000075982
2-hydroxymethyl-3,4,5-trihydroxy-N-methylpiperidine
SR-01000075982-1
(3R,5R)-2-Hydroxymethyl-1-methyl-piperidine-3,4,5-triol
Solubility of 2-(hydroxymethyl)-1-methyl-piperidine-3,4,5-triol
This compound, with the molecular formula C7H15NO4, exhibits notable solubility properties primarily due to its structural characteristics. The presence of multiple hydroxyl (-OH) groups in the molecule greatly enhances its solubility in water.
Factors Affecting Solubility
The solubility of 2-(hydroxymethyl)-1-methyl-piperidine-3,4,5-triol can be attributed to several key factors:
Moreover, it is generally observed that compounds with a high number of hydroxyl groups tend to be more soluble in aqueous solutions. As noted in various studies, compounds like 2-(hydroxymethyl)-1-methyl-piperidine-3,4,5-triol can show excellent solubility patterns, making them suitable for applications where aqueous media are involved.
Conclusion
In summary, the solubility of C7H15NO4 is significantly influenced by its functional groups and molecular structure. Its high solubility in water is key for its potential uses in pharmaceuticals and biochemical applications.