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Catalog Number:
41470
CAS Number:
140408-82-8
( S )-(-)-1,2,3,4-tétrahydro-α,α-diphényl-3-isoquinolineméthanol
Purity:
≥ 97%
Documents
$228.24 /1G
Taille
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Informations sur le produit

(S)-(-)-1,2,3,4-Tetrahydro-a,a-diphenyl-3-isoquinolinemethanol is a versatile compound recognized for its unique structural properties and potential applications in various fields. This chiral molecule is particularly valuable in pharmaceutical research, where it can serve as a building block for the synthesis of bioactive compounds. Its ability to interact with biological systems makes it a candidate for drug development, particularly in the areas of neuropharmacology and medicinal chemistry. Researchers have explored its efficacy in modulating neurotransmitter systems, which could lead to advancements in treatments for neurological disorders.

In addition to its pharmaceutical relevance, this compound's unique stereochemistry allows for targeted applications in asymmetric synthesis, enhancing the efficiency of producing enantiomerically pure substances. Its stability and compatibility with various reaction conditions make it an ideal choice for chemists looking to innovate in synthetic methodologies. With its promising applications and the potential for further exploration, (S)-(-)-1,2,3,4-Tetrahydro-a,a-diphenyl-3-isoquinolinemethanol stands out as a valuable asset for researchers and industry professionals alike.

Numéro CAS 
140408-82-8
Formule moléculaire
C 22 H 21 NON
Poids moléculaire 
315.41
Point de fusion 
104 - 107 °C (lit.)
Rotation optique 
[ á]22/D = 100 ° (C = 1 dans le méthanol)
Informations générales
Numéro CAS 
140408-82-8
Formule moléculaire
C 22 H 21 NON
Poids moléculaire 
315.41
Point de fusion 
104 - 107 °C (lit.)
Rotation optique 
[ á]22/D = 100 ° (C = 1 dans le méthanol)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

(S)-(-)-1,2,3,4-Tetrahydro-a,a-diphenyl-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 in the development of drugs targeting neurological disorders.
  • Organic Synthesis: It is employed in organic chemistry for creating complex molecules, providing a versatile building block for researchers looking to innovate new chemical entities.
  • Chiral Catalysis: The compound's chiral nature makes it valuable in asymmetric synthesis, allowing chemists to produce enantiomerically pure compounds more efficiently than with non-chiral alternatives.
  • Biological Research: It is used in studies exploring the interaction of isoquinoline derivatives with biological systems, aiding in the discovery of new therapeutic agents.
  • Material Science: The compound's unique properties contribute to the development of advanced materials, including polymers and coatings that require specific chemical characteristics.

Citations