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Catalog Number:
39427
CAS Number:
52193-85-8
( R )-(+)-1-(2-naphtyl)éthanol
Purity:
≥ 98% (CG)
Synonym(s):
( R )-(+)-α-méthyl-2-naphtalèneméthanol, ( R )-(+)-2-(1-hydroxyéthyl)naphtalène
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$399.90 /1G
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Informations sur le produit

(R)-(+)-1-(2-Naphthyl)ethanol is a chiral alcohol that serves as a valuable intermediate in the synthesis of various pharmaceuticals and fine chemicals. Known for its unique stereochemistry, this compound is particularly useful in asymmetric synthesis, enabling the production of enantiomerically pure compounds that are critical in drug development. Its ability to act as a chiral auxiliary makes it an essential tool for researchers aiming to enhance the efficacy and specificity of therapeutic agents.

In the pharmaceutical industry, (R)-(+)-1-(2-Naphthyl)ethanol has been utilized in the synthesis of anti-inflammatory and analgesic drugs, showcasing its relevance in addressing health challenges. Additionally, its applications extend to the development of agrochemicals and flavoring agents, where its aromatic properties contribute to the desired sensory profiles. With its versatile applications and significant role in enhancing compound selectivity, (R)-(+)-1-(2-Naphthyl)ethanol stands out as a key player in modern chemical synthesis.

Numéro CAS 
52193-85-8
Formule moléculaire
C12H12O
Poids moléculaire 
172.23
Point de fusion 
70 - 74 °C
Rotation optique 
[α]20 D = 37 - 42 ° (C=1 dans le méthanol)
Informations générales
Numéro CAS 
52193-85-8
Formule moléculaire
C12H12O
Poids moléculaire 
172.23
Point de fusion 
70 - 74 °C
Rotation optique 
[α]20 D = 37 - 42 ° (C=1 dans le méthanol)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

(R)-(+)-1-(2-Naphthyl)ethanol is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a chiral building block in the synthesis of various pharmaceuticals, enhancing the efficacy and safety profiles of drugs by improving their stereochemistry.
  • Flavor and Fragrance Industry: Its unique aromatic properties make it valuable in creating complex fragrances and flavors, providing a rich, naphthalene-like scent that is sought after in perfumes and food products.
  • Organic Synthesis: It is used in organic chemistry as a reagent for synthesizing other complex organic molecules, facilitating research in developing new materials and compounds.
  • Biochemical Research: The compound is utilized in studies investigating the interactions of chiral molecules with biological systems, aiding in drug design and understanding metabolic pathways.
  • Material Science: Its properties contribute to the development of advanced materials, particularly in creating polymers with specific optical and mechanical characteristics.

Citations