NP-MRD: Showing NP-Card for (1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene (NP0232223)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 13:23:17 UTC

Updated at

2022-09-06 13:23:17 UTC

NP-MRD ID

NP0232223

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene

Description

(2R)-2,5,5,8abeta-Tetramethyl-2alpha,4aalpha-epoxy-3,4,4a,5,6,8a-hexahydro-2H-1-benzopyran belongs to the class of organic compounds known as ketals. These are acetals derived from ketones by replacement of the oxo group by two hydrocarbyloxy groups R2C(OR)2 ( R not Hydrogen ). This term, once abandoned, has been reinstated as a subclass of acetals. (1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene is found in Cydonia oblonga. Based on a literature review very few articles have been published on (2R)-2,5,5,8abeta-Tetramethyl-2alpha,4aalpha-epoxy-3,4,4a,5,6,8a-hexahydro-2H-1-benzopyran.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 35 37  0  0  0  0  0  0  0  0999 V2000
   -1.8588   -1.3362   -1.1442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4612   -0.2524   -0.1320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1632   -0.6673    1.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0202    1.0556   -0.5662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0266    2.0216   -1.0861 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2139    2.0607   -0.6153 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5799    1.0996    0.4570 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2380    1.5608    1.8173 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9511    0.8230    0.2823 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0190   -0.3115   -0.5113 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1260   -0.3494   -1.4733 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9687   -1.5035    0.4359 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5210   -1.3633    0.9284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0077   -0.2442    0.0835 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7401   -0.4454   -1.1071 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8824   -2.3058   -0.5912 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2203   -1.3383   -2.0249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9394   -1.1217   -1.3809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2451   -0.7305    0.9115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8298   -1.6597    1.4700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0170    0.0790    1.9579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7759    0.8924   -1.3614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5567    1.5709    0.2781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3140    2.7231   -1.8769 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8767    2.7972   -1.0505 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2661    0.7476    2.5370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7082    2.1345    1.7989 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0194    2.3042    2.1533 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0558   -0.6758   -0.9677 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8862   -0.9859   -2.3484 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3235    0.6748   -1.8534 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6385   -1.3056    1.2809 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1435   -2.4486   -0.0765 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0006   -2.2905    0.6056 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4583   -1.2094    2.0017 H   0  0  0  0  0  0  0  0  0  0  0  0
 10 11  1  6
 10 12  1  0
 12 13  1  0
 14 13  1  1
 14 15  1  0
 14  7  1  0
  7  8  1  1
  7  9  1  0
  7  6  1  0
  6  5  2  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  1  0
 15 10  1  0
  9 10  1  0
  2 14  1  0
 11 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 12 33  1  0
 13 34  1  0
 13 35  1  0
  8 26  1  0
  8 27  1  0
  8 28  1  0
  6 25  1  0
  5 24  1  0
  4 22  1  0
  4 23  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
M  END


  Mrv1652309062215232D          

 15 17  0  0  1  0            999 V2000
    2.2663    2.7231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9752    1.9512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2754    2.3882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7976    1.8159    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1079    1.0346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6172    0.3782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7973    0.5555    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0210   -0.2386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2143   -0.0011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5982    0.5318    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1384   -0.1532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0973    0.8845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3286    1.6443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4041    1.3454    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8305    1.4948    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
  2 14  1  0  0  0  0
  7 14  1  0  0  0  0
 14 15  1  6  0  0  0
 10 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0232223

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@]12CC[C@]3(O1)[C@@](C)(O2)C=CCC3(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C13H20O2/c1-10(2)6-5-7-11(3)13(10)9-8-12(4,14-11)15-13/h5,7H,6,8-9H2,1-4H3/t11-,12+,13+/m0/s1

> <INCHI_KEY>
QXHORPLJTIHQGR-YNEHKIRRSA-N

> <FORMULA>
C13H20O2

> <MOLECULAR_WEIGHT>
208.301

> <EXACT_MASS>
208.146329884

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
23.699622469000367

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,6S,8R)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0^{1,6}]undec-4-ene

> <JCHEM_LOGP>
2.8128595783333337

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.112339254337954

> <JCHEM_POLAR_SURFACE_AREA>
18.46

> <JCHEM_REFRACTIVITY>
59.941300000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,6S,8R)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0^{1,6}]undec-4-ene

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       4.230   5.083   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.687   3.642   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.381   4.458   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.222   3.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.801   1.931   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.885   0.706   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.355   1.037   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.773  -0.445   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.267  -0.002   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.117   0.993   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.258  -0.286   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.182   1.651   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.613   3.069   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.621   2.511   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.550   2.790   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   14                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   14                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   12   15                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    2    7   15                                             
CONECT   15   14   10                                                       
MASTER        0    0    0    0    0    0    0    0   15    0   34    0
END

View in JSmol

Synonyms

Value	Source
(2R)-2,5,5,8Abeta-tetramethyl-2a,4aalpha-epoxy-3,4,4a,5,6,8a-hexahydro-2H-1-benzopyran	Generator
(2R)-2,5,5,8Abeta-tetramethyl-2α,4aalpha-epoxy-3,4,4a,5,6,8a-hexahydro-2H-1-benzopyran	Generator

Chemical Formula

C₁₃H₂₀O₂

Average Mass

208.3010 Da

Monoisotopic Mass

208.14633 Da

IUPAC Name

(1R,6S,8R)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0^{1,6}]undec-4-ene

Traditional Name

(1R,6S,8R)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0^{1,6}]undec-4-ene

CAS Registry Number

Not Available

SMILES

C[C@]12CC[C@]3(O1)[C@@](C)(O2)C=CCC3(C)C

InChI Identifier

InChI=1S/C13H20O2/c1-10(2)6-5-7-11(3)13(10)9-8-12(4,14-11)15-13/h5,7H,6,8-9H2,1-4H3/t11-,12+,13+/m0/s1

InChI Key

QXHORPLJTIHQGR-YNEHKIRRSA-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

Species Name	Source	Reference
Cydonia oblonga	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ketals. These are acetals derived from ketones by replacement of the oxo group by two hydrocarbyloxy groups R2C(OR)2 ( R not Hydrogen ). This term, once abandoned, has been reinstated as a subclass of acetals.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Ketals

Alternative Parents

Substituents

Ketal
Oxane
Oxolane
Meta-dioxolane
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
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	2.81	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	18.46 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	59.94 m³·mol⁻¹	ChemAxon
Polarizability	23.7 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

10271234

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21636591

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene (NP0232223)

MOL for NP0232223 ((1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene)

3D MOL for NP0232223 ((1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene)

3D SDF for NP0232223 ((1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene)

3D-SDF for NP0232223 ((1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene)

PDB for NP0232223 ((1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene)

3D PDB for NP0232223 ((1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene)

SMILES for NP0232223 ((1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene)

INCHI for NP0232223 ((1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene)

Structure for NP0232223 ((1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene)

3D Structure for NP0232223 ((1r,6s,8r)-2,2,6,8-tetramethyl-7,11-dioxatricyclo[6.2.1.0¹,⁶]undec-4-ene)