Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
32457
CAS Number:
5949-11-1
Monochlorhydrate de cinchonine hydraté
Purity:
≥ 99 % (HPLC, T)
Synonym(s):
Monochlorhydrate de cinchonan-9( S -ol)
Documents
$22.03 /5G
Taille
Request Bulk Quote
Product Information

Conserver le récipient bien fermé dans un endroit sec et bien aéré.

Synonyms
Monochlorhydrate de cinchonan-9( S -ol)
CAS Number
5949-11-1
Purity
≥ 99 % (HPLC, T)
Molecular Formula
C19H22N2O · HCl · H2O
Molecular Weight
330.86
MDL Number
MFCD00191936
PubChem ID
3035282
Melting Point
208-218 ?C
Appearance
Poudre blanche
Optical Rotation
[a]20/D= +101° (C = 1 dans CHCl 3 )
Conditions
Magasin chez RT
General Information
Synonyms
Monochlorhydrate de cinchonan-9( S -ol)
CAS Number
5949-11-1
Purity
≥ 99 % (HPLC, T)
Molecular Formula
C19H22N2O · HCl · H2O
Molecular Weight
330.86
MDL Number
MFCD00191936
PubChem ID
3035282
Melting Point
208-218 ?C
Appearance
Poudre blanche
Optical Rotation
[a]20/D= +101° (C = 1 dans CHCl 3 )
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Cinchonine monohydrochloride hydrate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is integral in the synthesis of various medications, particularly in the treatment of malaria and other parasitic infections, enhancing therapeutic efficacy.
  • Analytical Chemistry: It serves as a chiral resolving agent in chromatography, helping researchers separate enantiomers effectively, which is crucial for drug formulation and quality control.
  • Natural Product Synthesis: Used as a building block in the synthesis of complex natural products, it aids chemists in developing new compounds with potential medicinal properties.
  • Biochemical Research: Its role as a ligand in biochemical assays allows for the study of various biological processes, providing insights into enzyme activity and receptor interactions.
  • Organic Synthesis: Cinchonine monohydrochloride hydrate is employed in asymmetric synthesis, offering advantages in producing compounds with high optical purity, which is essential in pharmaceuticals.

Citations