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tert-Butyl (R)-3-methoxypyrrolidine-1-carboxylate

  • CAS No. 549532-08-3

  • Cat. No. CS-0079250
  • Molecule weightNone
  • Purity≥95%
  • MDL No.MFCD16620894

*For research and further manufacturing use only, not for direct human use.

tert-Butyl (R)-3-methoxypyrrolidine-1-carboxylate|CS-0079250

Structure of 549532-08-3

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General Information

  • CAS No. 549532-08-3
  • Cat. No. CS-0079250
  • Purity ≥95%
  • MDL No. MFCD16620894
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₉NO₃
  • Molecular Weight None
  • Synonym(s) (R)-tert-Butyl 3-Methoxypyrrolidine-1-carboxylate
  • SMILES O=C(N1C[C@H](OC)CC1)OC(C)(C)C

Description

This chiral tert-butyl (R)-3-methoxypyrrolidine-1-carboxylate features a stereodefined pyrrolidine core with a bench-stable carbamate protecting group, enabling direct incorporation into asymmetric synthesis. The methoxy substituent enhances solubility and modulates electronic properties, facilitating efficient coupling reactions in medicinal chemistry applications.

Application

tert-Butyl (R)-3-methoxypyrrolidine-1-carboxylate serves as a stereochemically defined building block for the synthesis of bioactive nitrogen heterocycles. Its pyrrolidine core exhibits robust bench stability and tolerates diverse reaction conditions, enabling efficient functionalization at the 3-position. The tert-butyl carbamate group provides orthogonal protection compatible with standard deprotection protocols, facilitating downstream coupling and cyclization reactions in medicinal chemistry campaigns.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P302+P352-P304+P340

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Computational Chemistry Data

  • TPSA   38.77
  • LogP   1.6422
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   1

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