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Catalog Number:
39516
CAS Number:
7322-88-5
Ácido (+)- O -acetil-L-mandélico
Purity:
≥ 98% (Ensayo por titulación)
Synonym(s):
( S )-(+)-ácido α-acetoxifenilacético
Documents
$80.62 /5G
Tamaño
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Información del producto

(+)-O-Acetyl-L-mandelic acid is a versatile compound widely recognized for its applications in the pharmaceutical and chemical industries. This chiral molecule, characterized by its acetyl and phenyl groups, serves as a valuable intermediate in the synthesis of various pharmaceuticals, particularly in the production of chiral drugs. Its unique structure allows for selective reactions that are essential in the development of enantiomerically pure compounds, making it a crucial building block for researchers focused on drug development and synthesis.

In addition to its pharmaceutical relevance, (+)-O-Acetyl-L-mandelic acid is utilized in the synthesis of flavoring agents and fragrances, capitalizing on its pleasant aroma and taste profile. Its ability to act as a chiral auxiliary further enhances its appeal in asymmetric synthesis, providing researchers with a reliable tool for creating complex molecules with high specificity. The compound's stability and ease of handling make it an ideal choice for both laboratory and industrial applications, ensuring that it meets the rigorous demands of modern chemical synthesis.

Número CAS
7322-88-5
Fórmula molecular
C10H10O4
Peso molecular
194.19
Número MDL
MFCD00064215
Punto de fusión
96 - 102 °C
Rotación óptica
[α]20 D = 151 - 155 ° (C=2 en Acetona)
Condiciones
Tienda en RT
Información general
Número CAS
7322-88-5
Fórmula molecular
C10H10O4
Peso molecular
194.19
Número MDL
MFCD00064215
Punto de fusión
96 - 102 °C
Rotación óptica
[α]20 D = 151 - 155 ° (C=2 en Acetona)
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

(+)-O-Acetyl-L-mandelic acid is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting metabolic disorders.
  • Chiral Synthesis: It is used in asymmetric synthesis processes, allowing chemists to create specific enantiomers that are crucial in the production of effective medications.
  • Analytical Chemistry: The compound is employed in analytical methods to determine the presence of certain biological molecules, enhancing the accuracy of biochemical assays.
  • Cosmetic Formulations: Its properties make it suitable for use in cosmetics, where it can act as a stabilizer or pH adjuster, improving product performance and shelf life.
  • Research in Metabolism: Researchers utilize this compound to study metabolic pathways, providing insights into how certain substances are processed in the body, which is vital for drug development and safety assessments.

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