tert-Butyl isoxazol-3-ylcarbamate
Names and Identifiers of tert-Butyl isoxazol-3-ylcarbamate
CAS Number |
264600-97-7 |
|---|---|
MDL Number |
MFCD11100913 |
IUPAC Name |
tert-butyl N-(1,2-oxazol-3-yl)carbamate |
InChI |
InChI=1S/C8H12N2O3/c1-8(2,3)13-7(11)9-6-4-5-12-10-6/h4-5H,1-3H3,(H,9,10,11) |
InChIKey |
IBHBABFDCMKSOA-UHFFFAOYSA-N |
Canonical SMILES |
CC(C)(C)OC(=O)NC1=NOC=C1 |
UNSPSC Code |
12352100 |
Physical and chemical properties of tert-Butyl isoxazol-3-ylcarbamate
Exact Mass |
184.08500 |
|---|---|
LogP |
1.44350 |
Molecular Formula |
C8H12N2O3 |
Molecular Weight |
184.19200 |
PSA |
67.59000 |
Safety Information of tert-Butyl isoxazol-3-ylcarbamate
Interaction Studies of tert-Butyl isoxazol-3-ylcarbamate
Studies have shown that tert-butyl isoxazol-3-ylcarbamate interacts with various biological targets, including enzymes involved in metabolic processes and signaling pathways. These interactions can lead to inhibition or modulation of biological functions, making this compound significant in therapeutic contexts.
Biological Activity of tert-Butyl isoxazol-3-ylcarbamate
Compounds featuring the isoxazole moiety, including tert-butyl isoxazol-3-ylcarbamate, exhibit a range of biological activities. They have been studied for their potential as herbicides and as inhibitors in various biological pathways, particularly in cancer research. The biological activity often correlates with their ability to interact with specific enzymes or receptors, such as vascular endothelial growth factor receptor 2 (VEGFR-2), which plays a crucial role in angiogenesis.
Physical sample testing spectrum (NMR) of tert-Butyl isoxazol-3-ylcarbamate
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