4-(N-BOC-AMINO)PIPERIDINE
Suppliers
Names
[ CAS No. ]:
73874-95-0
[ Name ]:
4-(N-BOC-AMINO)PIPERIDINE
[Synonym ]:
2-Methyl-2-propanyl 4-amino-1-piperidinecarboxylate
Carbamic acid, N-4-piperidinyl-, 1,1-dimethylethyl ester
MFCD00798171
methanol, 1-(1,1-dimethylethoxy)-1-(4-piperidinylimino)-, (E)-
tert-butyl N-piperidin-4-ylcarbamate
tert-butyl-piperidin-4-ylcarbamat
2-Methyl-2-propanyl 4-piperidinylcarbamate
tert-butyl piperidin-4-ylcarbamate
4-(N-BOC-AMINO)PIPERIDINE
4-(tert-Butoxycarbonyl)-aminopiperidine
4-N-BOC-Aminopiperidine
4-N-(tert-Butoxycarbonyl)aminopiperidine
Chemical & Physical Properties
[ Density]:
1.0±0.1 g/cm3
[ Boiling Point ]:
304.8±31.0 °C at 760 mmHg
[ Melting Point ]:
162-166 °C(lit.)
[ Molecular Formula ]:
C10H20N2O2
[ Molecular Weight ]:
200.28
[ Flash Point ]:
138.2±24.8 °C
[ Exact Mass ]:
200.152481
[ PSA ]:
50.36000
[ LogP ]:
1.32
[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C
[ Index of Refraction ]:
1.480
MSDS
Safety Information
[ 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-S37/39
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2933399090
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Customs
[ 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%
Articles
J. Med. Chem. 49 , 2784, (2006)
We incorporated various polar groups into previously described piperidine-4-carboxamide CCR5 antagonists to improve their metabolic stability in human hepatic microsomes. Introducing a carbamoyl group...
Bioorg. Med. Chem. 11 , 1873-1881, (2003)
A series of oxindole CDK2 inhibitors was synthesized. These novel analogues have a saturated monosubstituted cyclic moiety at their C-4 position that mimics the ribofuranoside of ATP. This substitutio...
Poly (2-isopropyl-2-oxazoline)-poly (L-glutamate) block copolymers through ammonium-mediated NCA polymerization. Meyer M and Schlaad H.Macromolecules 39(11) , 3967-3970, (2006)