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7-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine

  • CAS No. 865472-04-4

  • Cat. No. CS-0041926
  • Purity≥97%
  • MDL No.MFCD07374011

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

7-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine|CS-0041926

Structure of 865472-04-4

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General Information

  • CAS No. 865472-04-4
  • Cat. No. CS-0041926
  • Purity ≥97%
  • MDL No. MFCD07374011
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₂BrN
  • Molecular Weight 226.11
  • Synonym(s) 7-bromotetralin-1-amine
  • SMILES NC1CCCC2=C1C=C(Br)C=C2

Description

7-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine features a brominated tetrahydronaphthalene core with a primary amine at the 1-position, enabling direct functionalization in synthetic routes. The electron-rich aromatic system enhances reactivity in cross-coupling processes, while the amine group provides a handle for derivatization. This bench-stable scaffold serves as a key intermediate in medicinal chemistry and materials synthesis.

Application

7-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine serves as a versatile scaffold for medicinal chemistry and process development, enabling direct functionalization at the aromatic ring and amine handle. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient derivatization. The bromo group supports palladium-catalyzed cross-coupling, while the primary amine allows for amide formation, reductive amination, or sulfonamide synthesis—key transformations in API lead optimization and heterocycle construction.

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   26.02
  • LogP   2.7852
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   0

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