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Home > Encyclopedia > R-3-amino-1-N-Boc-piperidine

R-3-amino-1-N-Boc-piperidine

R-3-amino-1-N-Boc-piperidine structure

R-3-amino-1-N-Boc-piperidine 

structure

R-3-amino-1-N-Boc-piperidine Basic Attributes

200.28

200.152481

1312995-182-4

DTXSID90363570

2933399090

Characteristics

55.6

0.7

Colorless to pale yellow Liquid

1.0±0.1 g/cm3

121.5±25.4 °C

1.484

Immiscible with water.

Storeunderinertgas

28.5 º (c=1, DMF)

Safety Information

III

8

UN2735

3

22-36/37/38

26

Xn

P261-P305 + P351 + P338

H302-H315-H319-H335

|Warning|H302 (91.67%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 48 companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

R-3-amino-1-N-Boc-piperidine Use and Manufacturing

Method for producing (R)-1-(tert-butoxycarbonyl)-3-aminopiperidine To a solution (amount 9 g) of (R)-1-(tert-butoxy carbonyl)nipecotamide (net weigh of (R)-1-(tert-butoxycarbonyl) nipecotamide: 0.7 g), Sodium hydroxide (1.3 g, 10 equivalents) and an aqueous sodium hypochlorite solution (2.2 g, 1.1 equivalents) were added. The mixture was stirred at 15 to 25° C. for 16 hours. The water layer was removed, and the solvent was evaporated under reduced pressure. Toluene (10 ml) and saturated brine (5 ml) were added thereto, and the water layer was removed. The solvent was evaporated under reduced pressure to obtain the title compound as yellow oil (0.7 g, net weight: 0.5 g, yield: 80percent).

Computed Properties

Molecular Weight:200.28
XLogP3:0.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:200.152477885
Monoisotopic Mass:200.152477885
Topological Polar Surface Area:55.6
Heavy Atom Count:14
Complexity:211
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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