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CS-W001157 4
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tert-Butyl 4-amino-3,4-dihydroquinoline-1(2H)-carboxylate

  • CAS No. 944906-95-0

  • Cat. No. CS-W006926
  • Purity≥97%
  • MDL No.MFCD10697725

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

tert-Butyl 4-amino-3,4-dihydroquinoline-1(2H)-carboxylate|CS-W006926

Structure of 944906-95-0

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General Information

  • CAS No. 944906-95-0
  • Cat. No. CS-W006926
  • Purity ≥97%
  • MDL No. MFCD10697725
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₂₀N₂O₂
  • Molecular Weight 248.32
  • Synonym(s) tert-butyl 4-amino-3,4-dihydro-2H-quinoline-1-carboxylate
  • SMILES CC(C)(C)OC(=O)N1CCC(N)C2=C1C=CC=C2

Description

tert-Butyl 4-amino-3,4-dihydroquinoline-1(2H)-carboxylate features a bench-stable dihydroquinoline core with a strategically positioned amino group and a tert-butoxycarbonyl protecting group. This combination enables direct incorporation into synthetic sequences requiring nitrogen-directed functionalization or transition-metal-catalyzed coupling reactions. The protected amine facilitates downstream deprotection and derivatization under mild conditions.

Application

tert-Butyl 4-amino-3,4-dihydroquinoline-1(2H)-carboxylate serves as a versatile building block for medicinal chemistry, enabling efficient access to quinoline-based scaffolds through standard functional group manipulations. The protected amine and carboxylate functionalities offer orthogonal reactivity, supporting diverse coupling and derivatization strategies. Its bench-stable nature and compatibility with common reaction conditions facilitate straightforward purification and integration into multi-step syntheses.

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   55.56
  • LogP   2.8316
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   0

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