structure of tert-butyl N-[(1R)-1-ethyl-2-oxo-propyl]carbamate

tert-butyl N-[(1R)-1-ethyl-2-oxo-propyl]carbamate

CAS No.: 1000210-48-9
M. Wt: 201.26300
M. Fa: C10H19NO3
InChI Key: OYMVICMFVPPYRS-MRVPVSSYSA-N

Names and Identifiers of 1000210-48-9

CAS Number

1000210-48-9

IUPAC Name

tert-butyl N-[(3R)-2-oxopentan-3-yl]carbamate

InChI

InChI=1S/C10H19NO3/c1-6-8(7(2)12)11-9(13)14-10(3,4)5/h8H,6H2,1-5H3,(H,11,13)/t8-/m1/s1

InChIKey

OYMVICMFVPPYRS-MRVPVSSYSA-N

Canonical SMILES

CCC(C(=O)C)NC(=O)OC(C)(C)C

Isomeric SMILES

CC[C@H](C(=O)C)NC(=O)OC(C)(C)C

Physical and chemical properties of 1000210-48-9

Exact Mass

201.13600

LogP

2.26960

Molecular Formula

C10H19NO3

Molecular Weight

201.26300

PSA

55.40000

Safety Information of 1000210-48-9

Pictograms

Signal Word

 Warning

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of 1000210-48-9

Tert-butyl N-[(1R)-1-ethyl-2-oxo-propyl]carbamate finds applications in:

  • Pharmaceutical Development: It serves as an intermediate in the synthesis of bioactive compounds.
  • Agricultural Chemistry: Its derivatives may be explored for use as agrochemicals due to their biological activity.
  • Material Science: The compound can be utilized in developing polymers or coatings with specific properties.

Interaction Studies of 1000210-48-9

Interaction studies involving tert-butyl N-[(1R)-1-ethyl-2-oxo-propyl]carbamate have focused on its binding affinity to various biological targets. These studies aim to elucidate how this compound interacts with enzymes or receptors, potentially leading to new therapeutic applications. Preliminary results indicate that it may exhibit selective binding characteristics that could be harnessed for drug design.

Biological Activity of 1000210-48-9

Research indicates that tert-butyl N-[(1R)-1-ethyl-2-oxo-propyl]carbamate exhibits biological activity, particularly in medicinal chemistry. It has been studied for its potential as an anti-inflammatory agent and for its effects on various biological pathways. The specific mechanisms of action are still under investigation, but preliminary studies suggest that it may modulate certain enzyme activities or receptor interactions.