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tert-Butyl (1,2,3,4-tetrahydroquinolin-6-yl)carbamate

  • CAS No. 474539-25-8

  • Cat. No. CS-0063813
  • Purity≥96%
  • MDL No.MFCD02181066

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

tert-Butyl (1,2,3,4-tetrahydroquinolin-6-yl)carbamate|CS-0063813

Structure of 474539-25-8

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General Information

  • CAS No. 474539-25-8
  • Cat. No. CS-0063813
  • Purity ≥96%
  • MDL No. MFCD02181066
  • Storage RT, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₂₀N₂O₂
  • Molecular Weight 248.32
  • Synonym(s) Boc-6-amino-1,2,3,4-tetrahydroquinoline
  • SMILES O=C(OC(C)(C)C)NC1=CC2=C(NCCC2)C=C1

Description

tert-Butyl (1,2,3,4-tetrahydroquinolin-6-yl)carbamate serves as a protected amine derivative featuring a sterically hindered tert-butyl carbamate group attached to a tetrahydroquinoline scaffold. This stable, bench-ready reagent facilitates efficient incorporation of the tetrahydroquinolinyl moiety into complex molecular architectures, particularly in medicinal chemistry and natural product synthesis workflows.

Application

tert-Butyl (1,2,3,4-tetrahydroquinolin-6-yl)carbamate serves as a stable, bench-ready nitrogen protecting group for 1,2,3,4-tetrahydroquinoline derivatives. It facilitates selective functionalization at the C6 position and enables straightforward deprotection under mild acidic conditions. The carbamate moiety enhances solubility and stability during synthetic manipulations, making it ideal for use in medicinal chemistry campaigns targeting bioactive heterocycles.

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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   50.36
  • LogP   3.3917
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   1

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