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CAS 165950-84-5

:

1-Naphthalenol, 5,6,7,8-tetrahydro-6-(propylamino)-, hydrobromide (1:1), (6S)-

Description:
1-Naphthalenol, 5,6,7,8-tetrahydro-6-(propylamino)-, hydrobromide (1:1), (6S)-, with CAS number 165950-84-5, is a chemical compound characterized by its naphthalene-derived structure, which includes a tetrahydro configuration and a propylamino substituent. This compound is a hydrobromide salt, indicating that it is a protonated form of the base, which enhances its solubility in polar solvents. The presence of the naphthalenol moiety suggests potential applications in organic synthesis and medicinal chemistry, particularly due to its ability to participate in hydrogen bonding and its aromatic properties. The specific stereochemistry denoted by (6S) indicates a particular three-dimensional arrangement of atoms, which can influence the compound's biological activity and reactivity. As with many organic compounds, it is essential to handle this substance with care, considering its potential effects and interactions in biological systems. Further studies may be required to fully elucidate its properties and applications in various fields.
Formula:C13H19NO·BrH
InChI:InChI=1S/C13H19NO.BrH/c1-2-8-14-11-6-7-12-10(9-11)4-3-5-13(12)15;/h3-5,11,14-15H,2,6-9H2,1H3;1H/t11-;/m0./s1
InChI key:InChIKey=HUWWFOPCZSIFKK-MERQFXBCSA-N
SMILES:OC1=C2C(C[C@@H](NCCC)CC2)=CC=C1.Br
Synonyms:
  • (S)-5-Hydroxy-2-(N-propylamino)tetralin hydrobromide
  • (6S)-(-)-5-Hydroxy-N-propyl-2-aminotetralin hydrobromide
  • 1-Naphthalenol, 5,6,7,8-tetrahydro-6-(propylamino)-, hydrobromide (1:1), (6S)-
  • (S)-5,6,7,8-Tetrahydro-6-(propylamino)-1-naphthalenol hydrobromide
  • 1-Naphthalenol, 5,6,7,8-tetrahydro-6-(propylamino)-, hydrobromide, (S)-
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