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N-Boc-Nortropinone

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N-Boc-Nortropinone Basic information

Product Name:
N-Boc-Nortropinone
Synonyms:
  • BOC-NORTROPINONE
  • BOC-NTP
  • 8-BOC-8-AZABICYCLO[3.2.1]OCTAN-3-ONE
  • 8-AZABICYCLO[3.2.1]OCTAN-3-ONE, N-BOC PROTECTED
  • N-BOC-NORTROPINONE
  • TERT-BUTYL 3-OXO-8-AZABICYCLO[3.2.1]OCTANE-8-CARBOXYLATE
  • RARECHEM EM WB 0263
  • N-(tert-Butoxycarbonyl)nortropinone
CAS:
185099-67-6
MF:
C12H19NO3
MW:
225.28
EINECS:
626-467-6
Product Categories:
  • Heterocyclic Compounds
  • Heterocycle
  • pharmacetical
  • Various Intermediates
  • Heterocycles
  • Intermediates
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Fused Ring Systems
  • Novel building
  • null
Mol File:
185099-67-6.mol
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N-Boc-Nortropinone Chemical Properties

Melting point:
70-74 °C
Boiling point:
325.8±35.0 °C(Predicted)
Density 
1.139±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
form 
Solid
pka
-1.65±0.20(Predicted)
color 
Off-White
InChI
InChI=1S/C12H19NO3/c1-12(2,3)16-11(15)13-8-4-5-9(13)7-10(14)6-8/h8-9H,4-7H2,1-3H3
InChIKey
MENILFUADYEXNU-DTORHVGOSA-N
SMILES
C12N(C(OC(C)(C)C)=O)C(CC1)CC(=O)C2
CAS DataBase Reference
185099-67-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
41-36/37/38
Safety Statements 
26-39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29399990

MSDS

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N-Boc-Nortropinone Usage And Synthesis

Chemical Properties

Off-White Solid

Uses

N-Boc-Nortropinone is a 8-azabicyclo[3.2.1]octane derivative useful as opioid receptor modulator.

Definition

N-Boc-Nortropinone can be used for the preparation of Tropine derivatives. Tropine and its derivatives are a class of important heterocyclic compounds, which are alkaloids present in natural plants. Due to their diverse biological activities, they are widely used in the fields of pesticides, pharmaceuticals, and chemical industries. N-Boc-Nortropinone can also be used to synthesize a new bicyclic vinyl boronate[1].

References

[1] Shyamali Ghosh. “Convenient preparation of aryl-substituted nortropanes by SuzukiMiyaura methodology.” Canadian Journal of Chemistry 29 1 (2006): 555–560.

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