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Catalog Number:
41381
CAS Number:
51800-98-7
(+)-3-(Trifluoroacetil)alcanfor
Purity:
≥ 97,5 % (GC)
Synonym(s):
3-(trifluoroacetil)-D-alcanfor
Hazmat
Documents
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Tamaño
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Información del producto
Número CAS
51800-98-7
Fórmula molecular
C12H15F3O2
Peso molecular
0
Número MDL
MFCD00003746
Densidad
1,172 g/mL a 25 °C (Lit.)
Punto de ebullición
100 - 101 °C / 16 mmHg (Literatura)
Índice de refracción
n20D 1.451 (Literatura)
Rotación óptica
[α] 20 D = 142 - 154 ° (C = 2,3 en CH 2 Cl 2 )
Condiciones
Tienda en RT
Información general
Número CAS
51800-98-7
Fórmula molecular
C12H15F3O2
Peso molecular
0
Número MDL
MFCD00003746
Densidad
1,172 g/mL a 25 °C (Lit.)
Punto de ebullición
100 - 101 °C / 16 mmHg (Literatura)
Índice de refracción
n20D 1.451 (Literatura)
Rotación óptica
[α] 20 D = 142 - 154 ° (C = 2,3 en CH 2 Cl 2 )
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
-
Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

(+)-3-(Trifluoroacetyl)camphor is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in creating compounds with enhanced biological activity.
  • Flavor and Fragrance Industry: Its unique scent profile makes it a valuable ingredient in the formulation of perfumes and flavorings, providing a fresh, camphoraceous note that is sought after in many products.
  • Analytical Chemistry: Used as a chiral selector in chromatography, it helps in the separation of enantiomers, which is crucial for the development of chiral drugs and ensuring their efficacy and safety.
  • Material Science: The compound is explored in the development of new materials, particularly in coatings and polymers, where its properties can enhance durability and resistance to environmental factors.
  • Research in Organic Synthesis: It acts as a reagent in various organic reactions, facilitating the formation of complex molecules and aiding researchers in the exploration of new synthetic pathways.

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