1-(methoxymethyl)-1H-pyrazol-4-amine
Names and Identifiers of 1-(methoxymethyl)-1H-pyrazol-4-amine
CAS Number |
1001500-80-6 |
|---|---|
EC Number |
821-553-1 |
MDL Number |
MFCD04969823 |
IUPAC Name |
1-(methoxymethyl)pyrazol-4-amine |
InChI |
InChI=1S/C5H9N3O/c1-9-4-8-3-5(6)2-7-8/h2-3H,4,6H2,1H3 |
InChIKey |
MIBJLZRVWQFOMK-UHFFFAOYSA-N |
Canonical SMILES |
COCN1C=C(C=N1)N |
UNSPSC Code |
12352100 |
Physical and chemical properties of 1-(methoxymethyl)-1H-pyrazol-4-amine
Acidity coefficient |
3.29±0.15(Predicted) |
|---|---|
Boiling Point |
254.3±20.0 °C(Predicted) |
Density |
1.24±0.1 g/cm3(Predicted) |
Exact Mass |
127.07500 |
LogP |
0.65040 |
Molecular Formula |
C5H9N3O |
Molecular Weight |
127.14400 |
PSA |
53.07000 |
Storage condition |
2-8°C(protect from light) |
Safety Information of 1-(methoxymethyl)-1H-pyrazol-4-amine
Applications of 1-(methoxymethyl)-1H-pyrazol-4-amine
1-(Methoxymethyl)-1H-pyrazol-4-amine has various applications across multiple fields:
- Organic Synthesis: It serves as a building block for more complex organic molecules.
- Pharmaceutical Development: Investigated for potential therapeutic uses, particularly in anti-inflammatory and anti-cancer drugs.
- Material Science: Utilized in developing new materials with specific properties due to its unique chemical structure.
Interaction Studies of 1-(methoxymethyl)-1H-pyrazol-4-amine
Studies on the interactions of 1-(methoxymethyl)-1H-pyrazol-4-amine reveal its ability to bind with specific molecular targets, such as proteins involved in inflammatory pathways or cancer cell proliferation. Understanding these interactions is essential for elucidating its potential therapeutic mechanisms and optimizing its efficacy in drug formulations.
Biological Activity of 1-(methoxymethyl)-1H-pyrazol-4-amine
Research indicates that 1-(methoxymethyl)-1H-pyrazol-4-amine exhibits potential biological activities. It has been investigated for its anti-inflammatory and anti-cancer properties, making it a candidate for drug development. The mechanism of action typically involves interaction with specific enzymes or receptors, modulating their activity and influencing various cellular processes.
Physical sample testing spectrum (NMR) of 1-(methoxymethyl)-1H-pyrazol-4-amine
