structure of (R)-tert-Butyl 1-ethylpyrrolidin-3-ylcarbamate

(R)-tert-Butyl 1-ethylpyrrolidin-3-ylcarbamate

CAS No.: 1001347-43-8
M. Wt: 214.30500
M. Fa: C11H22N2O2
InChI Key: WYPHJLKRZSTDMH-SECBINFHSA-N

Names and Identifiers of 1001347-43-8

CAS Number

1001347-43-8

MDL Number

MFCD18378146

IUPAC Name

tert-butyl N-[(3R)-1-ethylpyrrolidin-3-yl]carbamate

InChI

InChI=1S/C11H22N2O2/c1-5-13-7-6-9(8-13)12-10(14)15-11(2,3)4/h9H,5-8H2,1-4H3,(H,12,14)/t9-/m1/s1

InChIKey

WYPHJLKRZSTDMH-SECBINFHSA-N

Canonical SMILES

CCN1CCC(C1)NC(=O)OC(C)(C)C

Isomeric SMILES

CCN1CC[C@H](C1)NC(=O)OC(C)(C)C

UNSPSC Code

12352100

Physical and chemical properties of 1001347-43-8

Exact Mass

214.16800

LogP

1.93410

Molecular Formula

C11H22N2O2

Molecular Weight

214.30500

PSA

41.57000

Safety Information of 1001347-43-8

Pictograms

Signal Word

 Warning

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

Applications of 1001347-43-8

(R)-tert-Butyl 1-ethylpyrrolidin-3-ylcarbamate has potential applications in medicinal chemistry as an intermediate in drug development. Its unique structure may provide valuable insights into designing compounds that target specific biological pathways or receptors. Additionally, it can be utilized in organic synthesis processes where carbamate functionalities are required.

Interaction Studies of 1001347-43-8

While specific interaction studies focusing solely on (R)-tert-Butyl 1-ethylpyrrolidin-3-ylcarbamate are scarce, similar compounds have been shown to interact with various biological targets, including enzymes and receptors involved in neurotransmission and metabolic processes. Future studies could explore its binding affinity and activity against specific targets to better understand its pharmacological potential.

Retrosynthesis analysis of 1001347-43-8

  • Route#1

    Cas:122536-77-0
    Cas:1001347-43-8

  • Route#2

    Cas:122536-76-9
    Cas:1001347-43-8