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Catalog Number:
39512
CAS Number:
52950-19-3
Acide 2-chloro-L-mandélique
Purity:
≥ 98 % (dosage par titration, pureté chirale, GC)
Synonym(s):
Acide ( S )-2'-chloro-α-hydroxyphénylacétique
Documents
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Informations sur le produit

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.

Numéro CAS 
52950-19-3
Formule moléculaire
C8H7ClO3
Poids moléculaire 
186.59
Point de fusion 
119 - 123 °C
Rotation optique 
[α]20 D = 124 - 125 ° (C=3 dans H 2 O)
Informations générales
Numéro CAS 
52950-19-3
Formule moléculaire
C8H7ClO3
Poids moléculaire 
186.59
Point de fusion 
119 - 123 °C
Rotation optique 
[α]20 D = 124 - 125 ° (C=3 dans H 2 O)
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

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.

Citations