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Catalog Number:
39148
CAS Number:
14575-84-9
Sel d'ammonium de l'acide (+)-3-bromocamphre-8-sulfonique
Purity:
≥ 98 % (dosage par titration)
Synonym(s):
Sel d'ammonium de l'acide [(1 R )-(endo, anti )]-(+)-3-bromocamphre-8-sulfonique
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Informations sur le produit

(+)-3-Bromocamphor-8-sulfonic acid ammonium salt is a versatile compound widely recognized for its applications in organic synthesis and analytical chemistry. This ammonium salt derivative of bromocamphor is particularly valued for its ability to act as a chiral auxiliary, facilitating enantioselective reactions. Its unique structure allows for effective separation of enantiomers, making it an essential tool in the development of pharmaceuticals and agrochemicals. Researchers utilize this compound in asymmetric synthesis, where it aids in the production of optically active compounds, crucial for drug development and other applications requiring specific stereochemistry.

In addition to its role in synthesis, (+)-3-Bromocamphor-8-sulfonic acid ammonium salt is also employed in various analytical techniques, including chromatography and spectroscopy. Its stability and solubility in various solvents enhance its usability in laboratory settings. The compound's distinctive properties not only streamline research processes but also contribute to the efficiency of producing high-purity compounds. Overall, this compound stands out for its practical applications in both academic and industrial research, making it a valuable addition to any chemical inventory.

Numéro CAS 
14575-84-9
Formule moléculaire
C10H18BrNO4S
Poids moléculaire 
328.22
Point de fusion 
283 - 285 °C (déc.)
Rotation optique 
[α] 20 D = 84 - 87° (C = 4 dans H 2 O)
Informations générales
Numéro CAS 
14575-84-9
Formule moléculaire
C10H18BrNO4S
Poids moléculaire 
328.22
Point de fusion 
283 - 285 °C (déc.)
Rotation optique 
[α] 20 D = 84 - 87° (C = 4 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

(+)-3-Bromocamphor-8-sulfonic acid ammonium salt is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, facilitating the synthesis of various complex molecules, which is essential for developing new pharmaceuticals.
  • Chiral Catalysis: Its unique structure makes it an effective chiral auxiliary in asymmetric synthesis, allowing researchers to produce enantiomerically pure compounds more efficiently than with other chiral reagents.
  • Biochemical Research: The compound is used in studies involving enzyme inhibition and protein interactions, helping scientists understand biological processes and develop targeted therapies.
  • Material Science: It plays a role in the development of advanced materials, particularly in creating polymers with specific properties, which can be beneficial in various industrial applications.
  • Analytical Chemistry: This ammonium salt is employed in chromatography and other analytical techniques, aiding in the separation and identification of compounds in complex mixtures.

Citations