NP-MRD: Showing NP-Card for 8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one (NP0317904)

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Record Information

Version

2.0

Created at

2022-09-11 18:04:05 UTC

Updated at

2022-09-11 18:04:05 UTC

NP-MRD ID

NP0317904

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one

Description

8-Bromo-4,7-dimethoxy-7,8-dimethyl-2H,5H,7H,8H-pyrano[3,2-c]pyran-2-one belongs to the class of organic compounds known as pyranones and derivatives. Pyranones and derivatives are compounds containing a pyran ring which bears a ketone. 8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one is found in Fusarium tricinctum. 8-Bromo-4,7-dimethoxy-7,8-dimethyl-2H,5H,7H,8H-pyrano[3,2-c]pyran-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 33 34  0  0  0  0  0  0  0  0999 V2000
    4.3525    0.8415   -0.9169 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9657    0.7458   -1.0513 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2248    0.1964   -0.0142 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8014   -0.2556    1.1362 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9974   -0.7896    2.1231 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5623   -1.2045    3.1883 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7036   -0.8637    1.9634 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0879   -0.4503    0.8889 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8283    0.0910   -0.1294 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2099    0.5927   -1.3769 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1093    0.2764   -1.4329 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8203    0.4359   -0.2412 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4160    1.8113    0.3489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1389    0.5411   -0.5287 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7868   -0.4540   -1.1731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4195   -0.5744    0.7833 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6826   -2.0009    0.4504 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2508   -0.1118    2.4566 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.6839    1.2369    0.0696 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7980   -0.1617   -1.0286 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7122    1.5691   -1.6765 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8792   -0.1974    1.2765 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4196    1.6820   -1.4462 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6978    0.1521   -2.2741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3164    2.1560    0.9339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1359    2.5155   -0.4348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6143    1.6085    1.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8464   -1.4356   -0.7182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4649   -0.5725   -2.2525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8672   -0.1222   -1.2887 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8355   -2.6092    0.9116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5751   -2.3939    0.9906 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6445   -2.2550   -0.6102 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  6
 14 15  1  0
 12 16  1  0
 16 17  1  0
 16 18  1  1
  9  3  1  0
 16  8  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  4 22  1  0
 10 23  1  0
 10 24  1  0
 13 25  1  0
 13 26  1  0
 13 27  1  0
 15 28  1  0
 15 29  1  0
 15 30  1  0
 17 31  1  0
 17 32  1  0
 17 33  1  0
M  END


  Mrv1533004241507052D          

 18 19  0  0  0  0            999 V2000
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9559   -1.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4256   -2.0127    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2380   -2.1560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8163   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416   -2.3784    0.0000 Br  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
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 12 16  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0317904

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=O)OC2=C1COC(C)(OC)C2(C)Br

> <INCHI_IDENTIFIER>
InChI=1S/C12H15BrO5/c1-11(13)10-7(6-17-12(11,2)16-4)8(15-3)5-9(14)18-10/h5H,6H2,1-4H3

> <INCHI_KEY>
VELKRHLRXGRDEF-UHFFFAOYSA-N

> <FORMULA>
C12H15BrO5

> <MOLECULAR_WEIGHT>
319.151

> <EXACT_MASS>
318.010287

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
27.357121796603213

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-bromo-4,7-dimethoxy-7,8-dimethyl-2H,5H,7H,8H-pyrano[3,2-c]pyran-2-one

> <ALOGPS_LOGP>
2.33

> <JCHEM_LOGP>
1.4565868923333334

> <ALOGPS_LOGS>
-2.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9847654395654373

> <JCHEM_POLAR_SURFACE_AREA>
53.99000000000001

> <JCHEM_REFRACTIVITY>
70.0865

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.61e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-bromo-4,7-dimethoxy-7,8-dimethyl-5H-pyrano[3,2-c]pyran-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.518  -2.043   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.528  -3.757   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.044  -4.025   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.390  -4.440   0.000  0.00  0.00           C+0
HETATM   18 Br   UNK     0       1.944  -4.440   0.000  0.00  0.00          Br+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8    3   10                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   16                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14                                                            
CONECT   16   12    8   17   18                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₂H₁₅BrO₅

Average Mass

319.1510 Da

Monoisotopic Mass

318.01029 Da

IUPAC Name

8-bromo-4,7-dimethoxy-7,8-dimethyl-2H,5H,7H,8H-pyrano[3,2-c]pyran-2-one

Traditional Name

8-bromo-4,7-dimethoxy-7,8-dimethyl-5H-pyrano[3,2-c]pyran-2-one

CAS Registry Number

Not Available

SMILES

COC1=CC(=O)OC2=C1COC(C)(OC)C2(C)Br

InChI Identifier

InChI=1S/C12H15BrO5/c1-11(13)10-7(6-17-12(11,2)16-4)8(15-3)5-9(14)18-10/h5H,6H2,1-4H3

InChI Key

VELKRHLRXGRDEF-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
Fusarium tricinctum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranones and derivatives. Pyranones and derivatives are compounds containing a pyran ring which bears a ketone.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrans

Sub Class

Pyranones and derivatives

Direct Parent

Pyranones and derivatives

Alternative Parents

Substituents

Ketal
Alkyl aryl ether
Pyranone
Heteroaromatic compound
Vinylogous ester
Lactone
Acetal
Ether
Oxacycle
Organic oxygen compound
Organobromide
Organohalogen compound
Organooxygen compound
Hydrocarbon derivative
Alkyl halide
Alkyl bromide
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	2.33	ALOGPS
logP	1.46	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	53.99 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	70.09 m³·mol⁻¹	ChemAxon
Polarizability	27.36 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one (NP0317904)

MOL for NP0317904 (8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one)

3D MOL for NP0317904 (8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one)

3D SDF for NP0317904 (8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one)

3D-SDF for NP0317904 (8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one)

PDB for NP0317904 (8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one)

3D PDB for NP0317904 (8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one)

SMILES for NP0317904 (8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one)

INCHI for NP0317904 (8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one)

Structure for NP0317904 (8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one)

3D Structure for NP0317904 (8-bromo-4,7-dimethoxy-7,8-dimethyl-5h-pyrano[3,2-c]pyran-2-one)