Methyl Piperidine-2-carboxylate structure 
             | 
        Common Name | Methyl Piperidine-2-carboxylate | ||
|---|---|---|---|---|
| CAS Number | 32559-18-5 | Molecular Weight | 179.645 | |
| Density | N/A | Boiling Point | 235.3ºC at 760 mmHg | |
| Molecular Formula | C7H14ClNO2 | Melting Point | 205ºC (dec.)(lit.) | |
| MSDS | Chinese USA | Flash Point | 96.1ºC | |
| Symbol | 
             
            
            GHS07  | 
        Signal Word | Warning | |
| Name | methyl piperidine-2-carboxylate,hydrochloride | 
|---|---|
| Synonym | More Synonyms | 
| Boiling Point | 235.3ºC at 760 mmHg | 
|---|---|
| Melting Point | 205ºC (dec.)(lit.) | 
| Molecular Formula | C7H14ClNO2 | 
| Molecular Weight | 179.645 | 
| Flash Point | 96.1ºC | 
| Exact Mass | 179.071304 | 
| PSA | 38.33000 | 
| LogP | 1.43230 | 
| 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 | 
| Risk Phrases | R36/37/38 | 
| Safety Phrases | 26-37/39 | 
| RIDADR | NONH for all modes of transport | 
| HS Code | 2933399090 | 
| Precursor 3 | |
|---|---|
| DownStream 6 | |
| 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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                                    Aldehyde-based racemization in the dynamic kinetic resolution of N-heterocyclic a-amino esters using Candida Antarctica lipase A. Liljeblad A, et al.
                                    
                                    
                                     Tetrahedron 60(3) , 671-677, (2004) 
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                                    Enantioselective lipase-catalyzed reactions of methyl pipecolinate: transesterification and N-acylation. Liljeblad, A, et al.
                                    
                                    
                                     Tetrahedron Lett. 43(13) , 2471-2474, (2002) 
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                                    The α-effect in cyclic secondary amines: new scaffolds for iminium ion accelerated transformations. Brazier JB, et al.
                                    
                                    
                                     Tetrahedron 65(48) , 9961-9966, (2009) 
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| MFCD00192316 | 
| piperidine-2-carboxylic acid methyl ester hydrochloride | 
| 2-Piperidinecarboxylic acid, methyl ester, hydrochloride (1:1) | 
| methyl piperidine-2-carboxylate hydrochloride | 
| Methyl 2-piperidinecarboxylate hydrochloride (1:1) | 
| L-pipecolic acid methyl ester hydrochloride | 
| Methyl pipecolinate hydrochloride | 
| DL-pipecolic acid methyl ester hydrochloride | 
| Methyl 2-piperidinecarboxylate hydrochloride | 
| (S)-pipecolic acid methyl ester hydrochloride | 
| 2-piperidine-carboxylic acid methyl ester hydrochloride | 
| Methy pipecolinate HCl | 
| Methyl Piperidine-2-carboxylate |