NP-MRD: Showing NP-Card for [(1r,5r,7r)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol (NP0161556)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 19:45:45 UTC

Updated at

2022-09-02 19:45:45 UTC

NP-MRD ID

NP0161556

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1r,5r,7r)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol

Description

Bottrospicatol belongs to the class of organic compounds known as oxolanes. These are organic compounds containing an oxolane (tetrahydrofuran) ring, which is a saturated aliphatic five-member ring containing one oxygen and five carbon atoms. Based on a literature review very few articles have been published on Bottrospicatol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 28 29  0  0  0  0  0  0  0  0999 V2000
    3.2265    0.7527    0.2598 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9605    0.0869   -0.1359 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7529   -1.2121    0.0264 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3747   -1.8008    0.1244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6379   -0.9231   -0.5789 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1268   -0.1801   -1.6567 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8175    0.8582   -0.7553 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0667    1.1208    0.2580 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0920    0.2277    0.2569 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5440   -0.1820    1.6354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2915    0.8590   -0.4427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6223    2.0147    0.2985 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1610    1.8226    0.0396 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0535    0.3024   -0.3268 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4416    0.5625    1.3248 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6138   -1.8704    0.0904 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1338   -2.0115    1.1651 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3937   -2.7642   -0.4336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4524   -1.4963   -1.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5027    0.2879   -2.4153 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8882   -0.8596   -2.0928 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1635    1.7258   -1.3208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0119    0.7211    2.0991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7485   -0.5488    2.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3201   -0.9628    1.5317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0550    1.1727   -1.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1610    0.1585   -0.4385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6018    2.1383    0.2414 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  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  1
  9 11  1  0
 11 12  1  0
  7  2  1  0
  9  5  1  0
  1 13  1  0
  1 14  1  0
  1 15  1  0
  3 16  1  0
  4 17  1  0
  4 18  1  0
  5 19  1  6
  6 20  1  0
  6 21  1  0
  7 22  1  6
 10 23  1  0
 10 24  1  0
 10 25  1  0
 11 26  1  0
 11 27  1  0
 12 28  1  0
M  END


  Mrv1652309022221452D          

 12 13  0  0  1  0            999 V2000
    2.5944   -0.4728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0800    0.1722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4380    0.9155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0800    1.6588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2757    1.8423    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0440    0.9155    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2757   -0.0114    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6307    0.5030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6307    1.3280    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1941    1.3095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1309    1.9844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4495    2.7454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  7  6  1  1  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  1  0  0  0
 11 12  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0161556

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=CC[C@@H]2C[C@H]1O[C@@]2(C)CO

> <INCHI_IDENTIFIER>
InChI=1S/C10H16O2/c1-7-3-4-8-5-9(7)12-10(8,2)6-11/h3,8-9,11H,4-6H2,1-2H3/t8-,9-,10+/m1/s1

> <INCHI_KEY>
CTNONMWSJRMRCY-BBBLOLIVSA-N

> <FORMULA>
C10H16O2

> <MOLECULAR_WEIGHT>
168.236

> <EXACT_MASS>
168.115029755

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
28

> <JCHEM_AVERAGE_POLARIZABILITY>
18.917030132935846

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
[(1R,5R,7R)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol

> <ALOGPS_LOGP>
1.45

> <JCHEM_LOGP>
1.058280046333333

> <ALOGPS_LOGS>
-1.36

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.365002432209462

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0765479361515817

> <JCHEM_POLAR_SURFACE_AREA>
29.46

> <JCHEM_REFRACTIVITY>
48.010999999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.27e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(1R,5R,7R)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       4.843  -0.883   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.883   0.321   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.551   1.709   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.883   3.096   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.381   3.439   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.949   1.709   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.381  -0.021   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.177   0.939   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.177   2.479   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.362   2.444   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.244   3.704   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.839   5.125   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    9                                                  
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7    9                                                       
CONECT    9    8    5   10   11                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11                                                            
MASTER        0    0    0    0    0    0    0    0   12    0   26    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₀H₁₆O₂

Average Mass

168.2360 Da

Monoisotopic Mass

168.11503 Da

IUPAC Name

[(1R,5R,7R)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol

Traditional Name

[(1R,5R,7R)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol

CAS Registry Number

Not Available

SMILES

CC1=CC[C@@H]2C[C@H]1O[C@@]2(C)CO

InChI Identifier

InChI=1S/C10H16O2/c1-7-3-4-8-5-9(7)12-10(8,2)6-11/h3,8-9,11H,4-6H2,1-2H3/t8-,9-,10+/m1/s1

InChI Key

CTNONMWSJRMRCY-BBBLOLIVSA-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 oxolanes. These are organic compounds containing an oxolane (tetrahydrofuran) ring, which is a saturated aliphatic five-member ring containing one oxygen and five carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxolanes

Sub Class

Not Available

Direct Parent

Oxolanes

Alternative Parents

Substituents

Oxolane
Oxacycle
Ether
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
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	1.45	ALOGPS
logP	1.06	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Acidic)	14.37	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	29.46 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	48.01 m³·mol⁻¹	ChemAxon
Polarizability	18.92 Å³	ChemAxon
Number of Rings	2	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

C00000146

Chemspider ID

61405058

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

90476648

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(1r,5r,7r)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol (NP0161556)

MOL for NP0161556 ([(1r,5r,7r)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol)

3D MOL for NP0161556 ([(1r,5r,7r)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol)

3D SDF for NP0161556 ([(1r,5r,7r)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol)

3D-SDF for NP0161556 ([(1r,5r,7r)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol)

PDB for NP0161556 ([(1r,5r,7r)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol)

3D PDB for NP0161556 ([(1r,5r,7r)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol)

SMILES for NP0161556 ([(1r,5r,7r)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol)

INCHI for NP0161556 ([(1r,5r,7r)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol)

Structure for NP0161556 ([(1r,5r,7r)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol)

3D Structure for NP0161556 ([(1r,5r,7r)-4,7-dimethyl-6-oxabicyclo[3.2.1]oct-3-en-7-yl]methanol)