176210-35-8

Basic information

• Product Name: (1S,2R,9R)-2-METHYL-OCTAHYDRO-2H-QUINOLIZIDINE-1-METHANOL
• Synonyms: (1S,2R,9R)-2-METHYL-OCTAHYDRO-2H-QUINOLIZIDINE-1-METHANOL;Zinc04202580
• CAS NO: 176210-35-8
• Molecular Formula: C11H21NO
• Molecular Weight: 183.29
• Mol File: 176210-35-8.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1S,2R,9R)-2-METHYL-OCTAHYDRO-2H-QUINOLIZIDINE-1-METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2R,9R)-2-METHYL-OCTAHYDRO-2H-QUINOLIZIDINE-1-METHANOL(176210-35-8)
• EPA Substance Registry System: (1S,2R,9R)-2-METHYL-OCTAHYDRO-2H-QUINOLIZIDINE-1-METHANOL(176210-35-8)

Safety Data

• Hazardous Substances Data: 176210-35-8(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
(1S,2R,9R)-2-METHYL-OCTAHYDRO-2H-QUINOLIZIDINE-1-METHANOL is used as a chiral building block for the synthesis of complex organic molecules. Its unique structure allows for the creation of enantiomerically pure compounds, which are essential in various chemical reactions and pharmaceutical development.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (1S,2R,9R)-2-METHYL-OCTAHYDRO-2H-QUINOLIZIDINE-1-METHANOL is used as a key intermediate in the development of new drugs. Its chiral nature and functional groups make it a valuable component in the synthesis of biologically active molecules with potential therapeutic applications.
Used in Drug Development:
(1S,2R,9R)-2-METHYL-OCTAHYDRO-2H-QUINOLIZIDINE-1-METHANOL is utilized as a precursor in the design and synthesis of novel drug candidates. Its unique stereochemistry and functional groups can be leveraged to create molecules with specific biological activities, targeting various diseases and medical conditions.
Further research is necessary to fully understand the properties and potential uses of (1S,2R,9R)-2-METHYL-OCTAHYDRO-2H-QUINOLIZIDINE-1-METHANOL in these and other fields. Its chiral nature and structural features make it a promising candidate for various applications, but more studies are required to explore its full potential.

Upstream product

• 133634-31-8 3-(1,3-Dimethyl-4(S),5(S)-diphenylimidazolidin-2-yl)pyridine 
• 176210-24-5 1-(4-chlorobutanoyl)-3-(1,3-dimethyl-4(S),5(S)-diphenylimidazolidin-2-yl)-4(R)-methyl-1,4-dihydropyridine 
• 176210-28-9 1-(4-iodobutanoyl)-3-formyl-4(R)-methyl-1,4-dihydropyridine 
• 176210-26-7 1-(4-chlorobutanoyl)-3-formyl-4(R)-methyl-1,4-dihydropyridine 
• 176210-30-3 (1S,2R,9aR)-2-methyl-6-oxo-2,6,7,8,9,9a-hexahydro-1H-quinolizine-1-carbaldehyde 

Relevant articles and documents

Radical cyclizations of 1,4-dihydropyridines. Synthesis of chiral fused nitrogen heterocycles. Synthesis of lupinine and epilupinine

Radical cyclizations of 1-(4-iodoalkanoyl)-3-formyl-4-methyl-l,4- dihydropyridines are described and discussed. A regio and diasteroselective reaction is obtained under ultrasonic conditions. An application to the synthesis of lupinine and epilupinine is shown.

Preparation of chiral hexahydroquinolizinones and tetrahydroindolizinones by regio- and diastereoselective sonochemical cyclization of chiral dihydropyridines

Chiral hexahydroquinolizinones 13 and tetrahydroindolizinones 17 were prepared from functionalized chiral dihydropyridines by regio- and diastereoselective sonochemical cyclization.