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Catalog Number:
39512
CAS Number:
52950-19-3
Ácido 2-cloro-L-mandélico
Purity:
≥ 98% (ensayo por titulación, pureza quiral, GC)
Synonym(s):
Ácido ( S )-2'-cloro-α-hidroxifenilacético
Documents
$95.94 /5G
Tamaño
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Información del producto

2-Chloro-L-mandelic acid is a versatile compound recognized for its significant applications in pharmaceuticals and organic synthesis. This compound, a derivative of mandelic acid, features a unique chlorophenyl group that enhances its reactivity and utility in various chemical reactions. Its chiral nature makes it particularly valuable in the synthesis of optically active compounds, which are crucial in the development of chiral drugs. Researchers have utilized 2-Chloro-L-mandelic acid in the production of intermediates for anti-inflammatory and analgesic medications, showcasing its relevance in the pharmaceutical industry.

Additionally, this compound serves as a key building block in the synthesis of agrochemicals and fine chemicals, where its ability to undergo various transformations can lead to the creation of complex molecular architectures. Its favorable solubility and stability under a range of conditions further enhance its appeal for industrial applications. With its proven track record in both research and commercial settings, 2-Chloro-L-mandelic acid stands out as a reliable choice for professionals seeking efficient and effective solutions in their chemical processes.

Número CAS
52950-19-3
Fórmula molecular
C8H7ClO3
Peso molecular
186.59
Número MDL
MFCD00798437
Punto de fusión
119 - 123 °C
Rotación óptica
[α]20 D = 124 - 125 ° (C=3 en H 2 O)
Condiciones
Tienda en RT
Información general
Número CAS
52950-19-3
Fórmula molecular
C8H7ClO3
Peso molecular
186.59
Número MDL
MFCD00798437
Punto de fusión
119 - 123 °C
Rotación óptica
[α]20 D = 124 - 125 ° (C=3 en H 2 O)
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

2-Chloro-L-mandelic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic drugs.
  • Chiral Synthesis: Its chiral nature makes it valuable in asymmetric synthesis, allowing chemists to create specific enantiomers that are crucial for drug efficacy and safety.
  • Analytical Chemistry: Used as a reagent in analytical methods, it helps in the detection and quantification of other compounds, enhancing the accuracy of chemical analysis.
  • Biochemical Research: This chemical is employed in studies related to enzyme inhibition and metabolic pathways, providing insights into biological processes and potential therapeutic targets.
  • Agricultural Chemistry: It has applications in the formulation of agrochemicals, contributing to the development of safer and more effective pesticides and herbicides.

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