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Catalog Number:
39415
CAS Number:
100306-34-1
( S )-(-)-3-chloro-1-phényl-1-propanol
Purity:
≥ 98% (CG)
Synonym(s):
( S )-(-)-α-(2-chloroéthyl)alcool benzylique
Documents
$129.19 /1G
Taille
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Informations sur le produit

(S)-(-)-3-Chloro-1-phenyl-1-propanol is a versatile chiral compound with significant applications in the pharmaceutical and chemical industries. This compound is recognized for its role as an intermediate in the synthesis of various bioactive molecules, particularly in the production of chiral pharmaceuticals. Its unique chiral center allows for the development of enantiomerically pure compounds, which are crucial for enhancing the efficacy and safety of therapeutic agents.

In addition to its pharmaceutical applications, (S)-(-)-3-Chloro-1-phenyl-1-propanol is also utilized in organic synthesis and as a building block for agrochemicals. Researchers appreciate its ability to facilitate complex chemical transformations, making it a valuable asset in both academic and industrial laboratories. The compound's stability and reactivity profile further enhance its utility, enabling chemists to explore innovative pathways in synthetic chemistry.

Numéro CAS 
100306-34-1
Formule moléculaire
C9H11ClO
Poids moléculaire 
170.64
Point de fusion 
57 - 61 °C
Rotation optique 
[α]20 D = -25 ° (C=1 dans CHCl 3 )
Informations générales
Numéro CAS 
100306-34-1
Formule moléculaire
C9H11ClO
Poids moléculaire 
170.64
Point de fusion 
57 - 61 °C
Rotation optique 
[α]20 D = -25 ° (C=1 dans CHCl 3 )
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 
-
Applications

(S)-(-)-3-Chloro-1-phenyl-1-propanol is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as an important intermediate in the synthesis of various pharmaceutical agents, particularly in the development of analgesics and anti-inflammatory drugs.
  • Chiral Building Block: Its chiral nature makes it a valuable building block in asymmetric synthesis, allowing chemists to create compounds with specific stereochemistry, which is crucial in drug development.
  • Research in Organic Chemistry: It is frequently used in organic chemistry laboratories for teaching and research purposes, helping students and researchers understand reaction mechanisms and chirality.
  • Flavor and Fragrance Industry: The compound is also explored for its potential applications in the flavor and fragrance industry, where it can be used to create specific aromatic profiles.
  • Material Science: Its unique properties allow it to be incorporated into polymer formulations, enhancing material characteristics such as stability and performance in various applications.

Citations