NP-MRD: Showing NP-Card for 3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane (NP0258613)

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Record Information

Version

2.0

Created at

2022-09-08 00:09:26 UTC

Updated at

2022-09-08 00:09:26 UTC

NP-MRD ID

NP0258613

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane

Description

3-Oxa-1-azatricyclo[7.3.1.0⁵,¹³]Tridecane belongs to the class of organic compounds known as quinolidines. These are organic compounds containing a quinolidine or decahydroquinoline moiety, which is a bicyclic skeleton consisting of a piperidine fused to a cyclohexane ring. 3-Oxa-1-azatricyclo[7.3.1.0⁵,¹³]Tridecane is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 32 34  0  0  0  0  0  0  0  0999 V2000
    2.6739   -0.0505   -0.1210 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8177   -1.2219   -0.4891 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4912   -1.0672    0.2265 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3581   -2.2728    0.1752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8142   -2.0642    0.3138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3455   -0.7762   -0.1866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5027    0.3360   -0.1172 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9224    1.4722    0.5961 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4149    2.6099   -0.0107 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0623    2.5991   -0.2046 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6258    1.3528    0.2325 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0260    1.2757   -0.2849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1381    0.1714   -0.3544 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9863   -0.1663    0.9490 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5770   -0.0756   -0.7923 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3593   -2.1419   -0.1816 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6030   -1.2163   -1.5823 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7431   -0.8349    1.2991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1199   -2.8613   -0.7566 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0340   -2.9606    1.0111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3416   -2.8957   -0.2328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1504   -2.1975    1.3844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6664   -0.9160   -1.2615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3164   -0.5577    0.3473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0377    1.5442    0.5400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6165    1.4785    1.6646 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1135    2.7594   -1.3090 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3603    3.5069    0.2838 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6430    1.3084    1.3419 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1072    1.6615   -1.3395 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6335    2.0170    0.3150 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0807    0.1838   -1.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 11 13  1  0
 12  1  1  0
 13  3  1  0
 13  7  1  0
  1 14  1  0
  1 15  1  0
  2 16  1  0
  2 17  1  0
  3 18  1  1
  4 19  1  0
  4 20  1  0
  5 21  1  0
  5 22  1  0
  6 23  1  0
  6 24  1  0
  8 25  1  0
  8 26  1  0
 10 27  1  0
 10 28  1  0
 11 29  1  1
 12 30  1  0
 12 31  1  0
 13 32  1  6
M  END

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0       4.001  -0.770   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.668  -0.770   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2   12                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4   13                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   13                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11    1                                                       
CONECT   13   11    3    7                                                  
MASTER        0    0    0    0    0    0    0    0   13    0   30    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₁H₁₉NO

Average Mass

181.2790 Da

Monoisotopic Mass

181.14666 Da

IUPAC Name

3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane

Traditional Name

3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane

CAS Registry Number

Not Available

SMILES

C1CC2CCCN3COCC(C1)C23

InChI Identifier

InChI=1S/C11H19NO/c1-3-9-5-2-6-12-8-13-7-10(4-1)11(9)12/h9-11H,1-8H2

InChI Key

UMXDWOAONBMYJH-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as quinolidines. These are organic compounds containing a quinolidine or decahydroquinoline moiety, which is a bicyclic skeleton consisting of a piperidine fused to a cyclohexane ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Quinolidines

Sub Class

Not Available

Direct Parent

Quinolidines

Alternative Parents

Substituents

Quinolidine
Piperidine
Oxazinane
1,3-oxazinane
Hemiaminal
Oxacycle
Azacycle
Organic nitrogen compound
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Amine
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.03	ALOGPS
logP	1.88	ChemAxon
logS	-1.8	ALOGPS
pKa (Strongest Basic)	7.87	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	12.47 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	52.24 m³·mol⁻¹	ChemAxon
Polarizability	21.28 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

72775260

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane (NP0258613)

MOL for NP0258613 (3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane)

3D MOL for NP0258613 (3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane)

3D SDF for NP0258613 (3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane)

3D-SDF for NP0258613 (3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane)

PDB for NP0258613 (3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane)

3D PDB for NP0258613 (3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane)

SMILES for NP0258613 (3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane)

INCHI for NP0258613 (3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane)

Structure for NP0258613 (3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane)

3D Structure for NP0258613 (3-oxa-1-azatricyclo[7.3.1.0⁵,¹³]tridecane)