61832-52-8

Basic information

• Product Name: 4-piperidin-3-ylbenzene-1,2-diol hydrobromide
• CAS NO: 61832-52-8
• Molecular Formula: BrH*C₁₁H₁₅NO₂
• Molecular Weight: 274.1542
• Mol File: 61832-52-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 372.8°C at 760 mmHg
• Flash Point: 167.1°C
• Vapor Pressure: 4.37E-06mmHg at 25°C
• CAS DataBase Reference: 4-piperidin-3-ylbenzene-1,2-diol hydrobromide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-piperidin-3-ylbenzene-1,2-diol hydrobromide(61832-52-8)
• EPA Substance Registry System: 4-piperidin-3-ylbenzene-1,2-diol hydrobromide(61832-52-8)

Safety Data

• Hazardous Substances Data: 61832-52-8(Hazardous Substances Data)

Upstream product

• 62033-58-3 3-(3,4-dimethoxy-phenyl)-piperidine 
• 79445-45-7 3-(3,4-Dimethoxyphenyl)pyridine 
• 89980-69-8 3,4-dimethoxyphenylmagnesium bromide 
• 626-55-1 3-Bromopyridine 

Relevant articles and documents

3-Phenylpiperidines. Central Dopamine-Autoreceptor Stimulating Activity

Thirty compounds related to the selective dopamine-autoreceptor agonist 3-(3-hydroxyphenyl)-N-n-propylpiperidine have been synthesized and tested for central dopamine-autoreceptor stimulating activity.The 3-(3-hydroxyphenyl)piperidine moiety seems indispensable for high potency and selectivity.Introduction of an additional hydroxyl group into the 4-position of the aromatic ring gives a compound with dopaminergic activity but lacking selectivity for autoreceptors. 3-(3-Hydroxyphenyl)-N-n-propylpyrrolidine, 3-(3-hydroxy)-N-n-propylperhydroazepine, and 3-(3-hydroxyphenyl)quinuclidine were all inactive.The most potent compounds were the N-isopropyl-, N-n-butyl-, N-n-pentyl-, and N-phenethyl-substituted 3-(3-hydroxyphenyl)piperidine derivatives.None of the compounds investigated seemed to have central noradrenaline- or serotonin-receptor stimulating activity.