NP-MRD: Showing NP-Card for 2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol (NP0183241)

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Record Information

Version

2.0

Created at

2022-09-03 22:06:45 UTC

Updated at

2022-09-03 22:06:45 UTC

NP-MRD ID

NP0183241

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol

Description

Epoxy-linalool oxide belongs to the class of organic compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ). 2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol is found in Nelumbo nucifera. 2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol was first documented in 2009 (PMID: 19662581). Based on a literature review a small amount of articles have been published on epoxy-linalool oxide (PMID: 31414500).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 29 30  0  0  0  0  0  0  0  0999 V2000
   -4.0232    0.3517   -0.5617 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7104   -0.2515   -0.2183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6338   -1.0732    1.0302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6861   -0.0470   -1.0050 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3220   -0.6137   -0.7421 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6156    0.5645   -0.6139 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0426    0.1082   -0.3435 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0568   -0.6749    0.9424 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4063   -0.7963   -1.3672 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9455    1.2512   -0.3857 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6403    2.1152    0.8159 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8735    1.8784    0.3202 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3393    0.7075   -0.1664 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5853   -0.4137   -1.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8972    1.2177   -1.2567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5803    0.7026    0.3259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1976   -0.5047    1.8765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6453   -1.3905    1.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0547   -2.0121    0.8516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7748    0.5529   -1.9017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0030   -1.3197   -1.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3217   -1.1301    0.2354 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3320    1.2071    0.2446 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5909    1.2106   -1.5098 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9150   -1.7694    0.7526 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1886   -0.3783    1.5832 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0053   -0.5847    1.4961 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0686   -1.6944   -1.1299 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4150    2.7867   -0.0460 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  6
  7 10  1  0
 10 13  1  6
 13 12  1  0
 12 11  1  0
 12 10  1  0
 11 10  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  3 17  1  0
  3 18  1  0
  3 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
  8 27  1  0
  9 28  1  0
 12 29  1  6
M  END

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -6.160   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -6.160   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.874  -2.310   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.206  -2.310   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.000   0.000   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11   12   13                                             
CONECT   11   10   12                                                       
CONECT   12   11   10   13                                                  
CONECT   13   12   10                                                       
MASTER        0    0    0    0    0    0    0    0   13    0   28    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₀H₁₆O₃

Average Mass

184.2350 Da

Monoisotopic Mass

184.10994 Da

IUPAC Name

2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol

Traditional Name

2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol

CAS Registry Number

Not Available

SMILES

CC(C)=CCCC(C)(O)C12OC1O2

InChI Identifier

InChI=1S/C10H16O3/c1-7(2)5-4-6-9(3,11)10-8(12-10)13-10/h5,8,11H,4,6H2,1-3H3

InChI Key

ZVGWOCIJIRIBKL-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

Species Name	Source	Reference
Nelumbo nucifera	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tertiary alcohols. Tertiary alcohols are compounds in which a hydroxy group, -OH, is attached to a saturated carbon atom R3COH (R not H ).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Tertiary alcohols

Alternative Parents

Substituents

Tertiary alcohol
1,3-dioxetane
Oxacycle
Organoheterocyclic compound
Oxirane
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	2.37	ChemAxon
pKa (Strongest Acidic)	12.96	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	45.29 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	48.78 m³·mol⁻¹	ChemAxon
Polarizability	19.88 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	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

132277303

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Zhang X, Liu J, Wang Y, Chingin K, Hua R, Zhu L, Rahman MM, Frankevich V, Chen H: Floral volatiles identification and molecular differentiation of Osmanthus fragrans by neutral desorption extractive atmospheric pressure chemical ionization mass spectrometry. Rapid Commun Mass Spectrom. 2019 Dec 30;33(24):1861-1869. doi: 10.1002/rcm.8554. [PubMed:31414500 ]
Sforcin JM, Amaral JT, Fernandes A Jr, Sousa JP, Bastos JK: Lemongrass effects on IL-1beta and IL-6 production by macrophages. Nat Prod Res. 2009;23(12):1151-9. doi: 10.1080/14786410902800681. [PubMed:19662581 ]
LOTUS database [Link]

Showing NP-Card for 2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol (NP0183241)

MOL for NP0183241 (2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol)

3D MOL for NP0183241 (2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol)

3D SDF for NP0183241 (2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol)

3D-SDF for NP0183241 (2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol)

PDB for NP0183241 (2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol)

3D PDB for NP0183241 (2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol)

SMILES for NP0183241 (2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol)

INCHI for NP0183241 (2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol)

Structure for NP0183241 (2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol)

3D Structure for NP0183241 (2-{2,4-dioxabicyclo[1.1.0]butan-1-yl}-6-methylhept-5-en-2-ol)