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Catalog Number:
41466
CAS Number:
18881-17-9
( S )-(-)-1,2,3,4-tétrahydro-3-isoquinoléinéméthanol
Purity:
≥ 97 % (HPLC)
Synonym(s):
( S )-1,2,3,4-tétrahydroisoquinoléine-3-méthanol, ( S )-3-hydroxyméthyl-1,2,3,4-tétrahydroisoquinoléine
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$112.57 /1G
Taille
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Informations sur le produit

(S)-(-)-1,2,3,4-Tetrahydro-3-isoquinolinemethanol is a versatile compound with significant relevance in pharmaceutical research and development. This chiral molecule, known for its unique structure, serves as a valuable building block in the synthesis of various bioactive compounds. Its ability to act as a precursor in the development of isoquinoline derivatives makes it particularly useful in medicinal chemistry, where it has been explored for its potential therapeutic effects, including analgesic and anti-inflammatory properties. Researchers appreciate its role in drug discovery processes, especially in the design of novel agents targeting neurological disorders.

In addition to its applications in drug synthesis, (S)-(-)-1,2,3,4-Tetrahydro-3-isoquinolinemethanol is recognized for its favorable pharmacokinetic properties, which enhance its utility in formulating effective therapeutic agents. Its chiral nature allows for the development of enantiomerically pure compounds, which can lead to improved efficacy and reduced side effects in clinical applications. This compound stands out in the realm of isoquinoline derivatives, offering researchers and industry professionals a reliable option for advancing their projects in drug development and related fields.

Numéro CAS 
18881-17-9
Formule moléculaire
C 10 H 13 NON
Poids moléculaire 
163.22
Point de fusion 
114 - 116 °C (lit.)
Rotation optique 
[ á]22/D = 97 ° (C = 1 dans le méthanol)
Informations générales
Numéro CAS 
18881-17-9
Formule moléculaire
C 10 H 13 NON
Poids moléculaire 
163.22
Point de fusion 
114 - 116 °C (lit.)
Rotation optique 
[ á]22/D = 97 ° (C = 1 dans le méthanol)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

(S)-(-)-1,2,3,4-Tetrahydro-3-isoquinolinemethanol is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders. Its unique structure allows for the development of drugs with enhanced efficacy and reduced side effects.
  • Neuroscience Research: Researchers use this chemical to study its effects on neurotransmitter systems, which can lead to a better understanding of mental health conditions and the development of new therapeutic strategies.
  • Analytical Chemistry: The compound is employed in analytical methods to detect and quantify isoquinoline derivatives, aiding in quality control processes in the pharmaceutical industry.
  • Natural Product Synthesis: It is utilized in the synthesis of natural products that exhibit biological activity, making it valuable for researchers in medicinal chemistry and drug discovery.
  • Biochemical Studies: This chemical is used in various biochemical assays to explore its interaction with biological targets, providing insights into potential therapeutic applications.

Citations