![]() 2-Methyl-2-propanyl 1-pyrrolidinecarboxylate structure
|
Common Name | 2-Methyl-2-propanyl 1-pyrrolidinecarboxylate | ||
---|---|---|---|---|
CAS Number | 86953-79-9 | Molecular Weight | 171.237 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 221.4±9.0 °C at 760 mmHg | |
Molecular Formula | C9H17NO2 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 87.7±18.7 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Name | 1-Boc-Pyrrolidine |
---|---|
Synonym | More Synonyms |
Density | 1.0±0.1 g/cm3 |
---|---|
Boiling Point | 221.4±9.0 °C at 760 mmHg |
Molecular Formula | C9H17NO2 |
Molecular Weight | 171.237 |
Flash Point | 87.7±18.7 °C |
Exact Mass | 171.125931 |
PSA | 29.54000 |
LogP | 1.49 |
Vapour Pressure | 0.1±0.4 mmHg at 25°C |
Index of Refraction | 1.473 |
Symbol |
![]() GHS07 |
---|---|
Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter |
Hazard Codes | Xi:Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36 |
RIDADR | NA 1993 / PGIII |
WGK Germany | 3 |
HS Code | 2933990090 |
Precursor 10 | |
---|---|
DownStream 10 | |
HS Code | 2933990090 |
---|---|
Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
Enantioselective, palladium-catalyzed α-arylation of N-Boc pyrrolidine: in situ react IR spectroscopic monitoring, scope, and synthetic applications.
J. Org. Chem. 76(15) , 5936-53, (2011) A comprehensive study of the enantioselective Pd-catalyzed α-arylation of N-Boc pyrrolidine has been carried out. The protocol involves deprotonation of N-Boc pyrrolidine using s-BuLi/(-)-sparteine in... |
|
Asymmetric synthesis of enantioenriched (+)-elaeokanine A.
J. Org. Chem. 71(15) , 5674-8, (2006) The key transformation in the total synthesis of (+)-elaeokanine A was accomplished by asymmetric deprotonation of N-Boc pyrrolidine, followed by the reaction of the in situ generated enantioenriched ... |
|
Enantioselective, palladium-catalyzed α-arylation of N-boc-pyrrolidine. Campos KR, et al.
J. Am. Chem. Soc. 128(11) , 3538-3539, (2006)
|
tert-butyl pyrrolidine-1-carboxylate |
MFCD00216581 |