Tert-butyl n-{4-[2-(4-formylpiperazin-1-yl)-2-oxoethyl]phenyl}carbamate
Names and Identifiers of 1000932-68-2
CAS Number |
1000932-68-2 |
|---|---|
MDL Number |
MFCD09863392 |
IUPAC Name |
tert-butyl N-{4-[2-(4-formylpiperazin-1-yl)-2-oxoethyl]phenyl}carbamate |
InChI |
InChI=1S/C18H25N3O4/c1-18(2,3)25-17(24)19-15-6-4-14(5-7-15)12-16(23)21-10-8-20(13-22)9-11-21/h4-7,13H,8-12H2,1-3H3,(H,19,24) |
InChIKey |
WYVUZRZEPKMPFX-UHFFFAOYSA-N |
Canonical SMILES |
CC(C)(C)OC(=O)NC1=CC=C(CC(=O)N2CCN(C=O)CC2)C=C1 |
UNSPSC Code |
12352100 |
Physical and chemical properties of 1000932-68-2
H Bond Acceptors |
4 |
|---|---|
H Bond Donors |
1 |
LogP |
1.18767998266667 |
Molecular Formula |
C18H25N3O4 |
Molecular Weight |
347.4 |
Safety Information of 1000932-68-2
Applications of 1000932-68-2
tert-Butyl N-{4-[2-(4-formylpiperazin-1-yl)-2-oxoethyl]phenyl}carbamate has several applications across different fields:
- Chemistry: Used as an intermediate in the synthesis of more complex molecules and as a reagent in various organic reactions.
- Biology: Investigated for its potential as a biochemical probe or building block for biologically active compounds.
- Medicine: Explored for therapeutic properties, particularly in drug development and pharmacological research.
- Industry: Utilized in producing specialty chemicals and materials with specific functional properties.
Interaction Studies of 1000932-68-2
Interaction studies involving tert-butyl N-{4-[2-(4-formylpiperazin-1-yl)-2-oxoethyl]phenyl}carbamate focus on its ability to modulate biological pathways through interactions with enzymes or receptors. For example, research may assess how this compound affects enzyme activity or receptor binding affinity, contributing to understanding its potential therapeutic effects.
Biological Activity of 1000932-68-2
The biological activity of tert-butyl N-{4-[2-(4-formylpiperazin-1-yl)-2-oxoethyl]phenyl}carbamate has been explored in various contexts. Initial studies suggest that it may act as a biochemical probe or as a building block for biologically active compounds. The presence of the piperazine moiety is particularly noteworthy, as piperazine derivatives are often associated with pharmacological properties, including potential anxiolytic and antidepressant effects. Additionally, the compound may exhibit interactions with specific molecular targets such as enzymes or receptors, influencing their activity through binding interactions.
