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Catalog Number:
39418
CAS Number:
32189-36-9
Ácido 4-cloro-D-mandélico
Purity:
≥ 98% (ensayo por titulación, GC)
Synonym(s):
Ácido ( R )-2-(4-clorofenil)-2-hidroxiacético
Documents
$90.34 /1G
Tamaño
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Información del producto

4-Chloro-D-mandelic acid is a versatile compound recognized for its unique properties and applications in various fields, particularly in pharmaceuticals and organic synthesis. This aromatic compound features a chlorinated phenyl group, which enhances its reactivity and makes it an essential intermediate in the synthesis of chiral pharmaceuticals. Its ability to act as a chiral building block allows researchers to develop compounds with specific stereochemistry, crucial for the efficacy of many drugs.

In addition to its pharmaceutical applications, 4-Chloro-D-mandelic acid is also utilized in the production of agrochemicals and fine chemicals, where its reactivity can be harnessed for the development of novel compounds. Its distinct properties make it a valuable asset for researchers looking to innovate in drug formulation and chemical synthesis. The compound's stability and ease of handling further contribute to its appeal, ensuring that it meets the rigorous demands of both laboratory and industrial environments.

Número CAS
32189-36-9
Fórmula molecular
C8H7ClO3
Peso molecular
186.59
Número MDL
MFCD00798430
Punto de fusión
119 - 123 °C
Rotación óptica
[α]20 D = -132 a -140 ° (C=0,3 en EtOH)
Condiciones
Tienda en RT
Información general
Número CAS
32189-36-9
Fórmula molecular
C8H7ClO3
Peso molecular
186.59
Número MDL
MFCD00798430
Punto de fusión
119 - 123 °C
Rotación óptica
[α]20 D = -132 a -140 ° (C=0,3 en EtOH)
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

4-Chloro-D-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 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 in drug formulation.
  • Analytical Chemistry: Used as a standard in chromatographic techniques, it aids in the quantification of other compounds, ensuring accurate analysis in quality control processes.
  • Cosmetic Formulations: The compound is incorporated into skincare products for its potential skin-soothing properties, enhancing the effectiveness of formulations aimed at sensitive skin.
  • Research in Biochemistry: It is utilized in studies exploring metabolic pathways and enzyme interactions, providing insights into biochemical processes relevant to health and disease.

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