4-Phenylpiperidine structure 
             | 
        Common Name | 4-Phenylpiperidine | ||
|---|---|---|---|---|
| CAS Number | 771-99-3 | Molecular Weight | 161.243 | |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 259.9±29.0 °C at 760 mmHg | |
| Molecular Formula | C11H15N | Melting Point | 61-65 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 113.0±19.7 °C | |
| Symbol | 
             
            
            GHS07  | 
        Signal Word | Warning | |
| Name | 4-Phenylpiperidine | 
|---|---|
| Synonym | More Synonyms | 
| Density | 1.0±0.1 g/cm3 | 
|---|---|
| Boiling Point | 259.9±29.0 °C at 760 mmHg | 
| Melting Point | 61-65 °C(lit.) | 
| Molecular Formula | C11H15N | 
| Molecular Weight | 161.243 | 
| Flash Point | 113.0±19.7 °C | 
| Exact Mass | 161.120453 | 
| PSA | 12.03000 | 
| LogP | 2.39 | 
| Vapour Pressure | 0.0±0.5 mmHg at 25°C | 
| Index of Refraction | 1.522 | 
| Symbol | 
                                    
                                     
                                    
                                    GHS07  | 
                            
|---|---|
| Signal Word | Warning | 
| Hazard Statements | H315-H319-H335 | 
| Precautionary Statements | P261-P305 + P351 + P338 | 
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves | 
| Hazard Codes | Xi:Irritant; | 
| Risk Phrases | R36/37/38 | 
| Safety Phrases | S26-S36/37/39-S45-S37/39-S36/37 | 
| RIDADR | UN 2922 8/PG 2 | 
| WGK Germany | 3 | 
| RTECS | TM2625000 | 
| HS Code | 2933399090 | 
| Precursor 9 | |
|---|---|
| DownStream 10 | |
| HS Code | 2933399090 | 
|---|---|
| Summary | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% | 
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                                    A strategy for isotope containment during radiosynthesis--devolatilisation of bromobenzene by fluorous-tagging-Ir-catalysed borylation en route to the 4-phenylpiperidine pharmacophore.
                                    
                                    
                                     Org. Biomol. Chem. 6 , 4093-4095, (2008) Syntheses of two 4-phenylpiperidines from bromobenzene have been developed involving anchoring to a fluorous-tag, Ir-catalysed borylation, Pd- and Co-catalysed elaboration then traceless cleavage. Alt...  | 
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                                    Structure-activity studies of morphine fragments. I. 4-alkyl-4-(m-hydroxy-phenyl)-piperidines.
                                    
                                    
                                     Mol. Pharmacol. 34(3) , 363-76, (1988) The 4-(m-OH-phenyl)piperidines are a flexible fragment of the morphine/benzomorphan fused-ring opioids. Analogs in this family were synthesized with varying 4-alkyl substituents increasing in bulk fro...  | 
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                                    Radical-mediated nitrile translocation as the key step in the stereoselective transformation of 2-(4-chloro-2-cyanobutyl)aziridines to methyl cis-(1-arylmethyl-4-phenylpiperidin-2-yl)acetates.
                                    
                                    
                                     Org. Biomol. Chem. 10(16) , 3308-14, (2012) Non-activated 2-(4-chloro-2-cyano-2-phenylbutyl)aziridines were used as building blocks for the stereoselective synthesis of novel cis-2-cyanomethyl-4-phenylpiperidines via a microwave-assisted azirid...  | 
                                
| Piperidine,4-phenyl | 
| 4-phenylpiperazine | 
| MFCD00005957 | 
| 4-Ph-piperdine | 
| EINECS 212-243-1 | 
| 4-phenyl-piperidine |