32213-47-1

Basic information

• Product Name: threo-3-piperidino-2-methyl-1-phenyl-1-propanol
• CAS NO: 32213-47-1
• Molecular Weight: 233.354
• Mol File: 32213-47-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: threo-3-piperidino-2-methyl-1-phenyl-1-propanol(CAS DataBase Reference)
• NIST Chemistry Reference: threo-3-piperidino-2-methyl-1-phenyl-1-propanol(32213-47-1)
• EPA Substance Registry System: threo-3-piperidino-2-methyl-1-phenyl-1-propanol(32213-47-1)

Safety Data

• Hazardous Substances Data: 32213-47-1(Hazardous Substances Data)

Upstream product

• 14045-28-4 N-propionylpiperidine 
• 24956-53-4 1-(2-benzoylpropanoyl)piperidine 
• 116836-46-5 erythro-N-(3-hydroxy-2-methyl-3-phenylpropanoyl)piperidine 
• 98-88-4 benzoyl chloride 
• 116596-04-4 threo-N-(3-hydroxy-3-phenyl-2-methylpropanoyl)piperidine 

Downstream Products

• 66063-99-8 Carbamic acid 2-methyl-1-phenyl-3-piperidin-1-yl-propyl ester 
• 66063-99-8 Carbamic acid 2-methyl-1-phenyl-3-piperidin-1-yl-propyl ester 
• 80792-43-4 Carbonic acid 2-methyl-1-phenyl-3-piperidin-1-yl-propyl ester phenyl ester; hydrochloride 
• 80792-43-4 Carbonic acid 2-methyl-1-phenyl-3-piperidin-1-yl-propyl ester phenyl ester; hydrochloride 

Relevant articles and documents

Erythro-Directive Reduction of α-Substituted Alkanones by Means of Hydrosilanes in Acidic Media

Hydrosilane reduced α-oxy and α-amino ketones and β-keto acid derivatives in trifluoroacetic acid to afford the corresponding erythro alcohols with high diastereoselectivity.The reaction proceeded without racemization at the carbon α to the carbonyl group.The erythro-directive reduction was explained in terms of the proton-bridged Cram cyclic model and successfully applied to the synthesis of physiologically important amino alcohols such as l-ephedrine, l-methoxamine, and erythro-2-methyl-3-piperidino-1-phenylpropanol.

Highly Stereoselective Reduction of α-Substituted β-Keto Amides by Means of Hydrosilane/F- and Hydrosilane/H+ Reagent. A Practical Approach to Aldols of Both Threo and Erythro Configurations

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