NP-MRD: Showing NP-Card for (e)-[(2e)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine (NP0290021)

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Record Information

Version

2.0

Created at

2022-09-09 20:29:31 UTC

Updated at

2022-09-09 20:29:31 UTC

NP-MRD ID

NP0290021

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(e)-[(2e)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine

Description

(E)-[(2E)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine belongs to the class of organic compounds known as fluorobenzenes. Fluorobenzenes are compounds containing one or more fluorine atoms attached to a benzene ring. Based on a literature review very few articles have been published on (E)-[(2E)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092222292D          

 26 26  0  0  0  0            999 V2000
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.0125    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.0125    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.3000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -3.3000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -5.7750    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 42 42  0  0  0  0  0  0  0  0999 V2000
   -5.1857   -1.9211   -0.1215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5835   -0.7269    0.1817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9526   -0.1744    0.2768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4143    0.2664    0.3646 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1866    2.0761    0.5093 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -3.7194    0.2498   -1.0003 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5800    1.1013   -1.0957 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0549    0.8916   -3.0514 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -1.3199    0.8252   -0.3858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7580    1.7464    0.6704 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6693   -0.3238   -0.4507 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5924   -0.5189    0.2187 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3662   -1.5295    0.3741 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5914   -1.0808    1.2137 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5826   -0.9005    0.2817 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9397   -0.4935    0.3757 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9307   -1.4356   -0.0972 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4341   -2.6540   -0.3714 F   0  0  0  0  0  0  0  0  0  0  0  0
    7.2129   -1.0972   -0.2223 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1263   -2.0319   -0.6345 F   0  0  0  0  0  0  0  0  0  0  0  0
    7.6787    0.1782    0.0985 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9813    0.4414   -0.0476 F   0  0  0  0  0  0  0  0  0  0  0  0
    6.7356    1.0809    0.5361 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1613    2.3519    0.8018 F   0  0  0  0  0  0  0  0  0  0  0  0
    5.4148    0.7467    0.6677 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5623    1.7512    1.0610 F   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9094   -2.7120   -0.3763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1321   -2.2270   -0.1221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0214    0.6461   -0.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7377   -0.9401    0.0259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1540    0.2401    1.2798 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8329    0.0414    1.1915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5307   -0.8110   -1.3004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4836    0.5697   -1.7424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7682    2.1619   -1.0141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3319    2.6643    0.6972 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7841    1.2114    1.6718 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3181    1.9746    0.4740 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0994   -1.0891   -1.0684 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0883    0.4263    0.7067 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1337    0.2798   -0.0275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3594   -1.2553   -0.8275 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0
  2  1  2  3
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  2  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  2  0
 25 26  1  0
 25 16  1  0
  3 29  1  0
  3 30  1  0
  3 31  1  0
  1 27  1  0
  1 28  1  0
  4 32  1  1
  6 33  1  0
  6 34  1  0
  7 35  1  6
 10 36  1  0
 10 37  1  0
 10 38  1  0
 11 39  1  0
 12 40  1  0
 15 41  1  0
 15 42  1  0
M  END


  Mrv1652309092222292D          

 26 26  0  0  0  0            999 V2000
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -7.0125    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -7.0125    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.3000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -3.3000    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -5.7750    0.0000 F   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0290021

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)C(Br)CC(Br)C(\C)=C\C=N\OCC1=C(F)C(F)=C(F)C(F)=C1F

> <INCHI_IDENTIFIER>
InChI=1S/C17H16Br2F5NO/c1-8(2)11(18)6-12(19)9(3)4-5-25-26-7-10-13(20)15(22)17(24)16(23)14(10)21/h4-5,11-12H,1,6-7H2,2-3H3/b9-4+,25-5+

> <INCHI_KEY>
AABFPTARQKBOHY-IFXFFPLBSA-N

> <FORMULA>
C17H16Br2F5NO

> <MOLECULAR_WEIGHT>
505.121

> <EXACT_MASS>
502.951881

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
38.413408082793296

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(E)-[(2E)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine

> <JCHEM_LOGP>
6.093156657

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
1.9700866802942212

> <JCHEM_POLAR_SURFACE_AREA>
21.59

> <JCHEM_REFRACTIVITY>
98.10659999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(E)-[(2E)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667 -10.780   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334 -11.550   0.000  0.00  0.00           C+0
HETATM    5 Br   UNK     0      -1.334 -13.090   0.000  0.00  0.00          Br+0
HETATM    6  C   UNK     0       0.000 -10.780   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM    8 Br   UNK     0       1.334 -13.090   0.000  0.00  0.00          Br+0
HETATM    9  C   UNK     0       2.667 -10.780   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335 -10.780   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       6.668 -11.550   0.000  0.00  0.00           N+0
HETATM   14  O   UNK     0       8.002 -10.780   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.336  -8.470   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   18  F   UNK     0       8.002  -6.160   0.000  0.00  0.00           F+0
HETATM   19  C   UNK     0      10.669  -6.160   0.000  0.00  0.00           C+0
HETATM   20  F   UNK     0      10.669  -4.620   0.000  0.00  0.00           F+0
HETATM   21  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   22  F   UNK     0      13.337  -6.160   0.000  0.00  0.00           F+0
HETATM   23  C   UNK     0      12.003  -8.470   0.000  0.00  0.00           C+0
HETATM   24  F   UNK     0      13.337  -9.240   0.000  0.00  0.00           F+0
HETATM   25  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   26  F   UNK     0      10.669 -10.780   0.000  0.00  0.00           F+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   16   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₆Br₂F₅NO

Average Mass

505.1210 Da

Monoisotopic Mass

502.95188 Da

IUPAC Name

(E)-[(2E)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine

Traditional Name

(E)-[(2E)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine

CAS Registry Number

Not Available

SMILES

CC(=C)C(Br)CC(Br)C(\C)=C\C=N\OCC1=C(F)C(F)=C(F)C(F)=C1F

InChI Identifier

InChI=1S/C17H16Br2F5NO/c1-8(2)11(18)6-12(19)9(3)4-5-25-26-7-10-13(20)15(22)17(24)16(23)14(10)21/h4-5,11-12H,1,6-7H2,2-3H3/b9-4+,25-5+

InChI Key

AABFPTARQKBOHY-IFXFFPLBSA-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 fluorobenzenes. Fluorobenzenes are compounds containing one or more fluorine atoms attached to a benzene ring.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Halobenzenes

Direct Parent

Fluorobenzenes

Alternative Parents

Substituents

Fluorobenzene
Aryl halide
Aryl fluoride
Oxime ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organofluoride
Organobromide
Organohalogen compound
Alkyl halide
Alkyl bromide
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	6.09	ChemAxon
pKa (Strongest Basic)	1.97	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	21.59 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	98.11 m³·mol⁻¹	ChemAxon
Polarizability	38.41 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

17342818

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

16215164

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (e)-[(2e)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine (NP0290021)

MOL for NP0290021 ((e)-[(2e)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine)

3D MOL for NP0290021 ((e)-[(2e)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine)

3D SDF for NP0290021 ((e)-[(2e)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine)

3D-SDF for NP0290021 ((e)-[(2e)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine)

PDB for NP0290021 ((e)-[(2e)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine)

3D PDB for NP0290021 ((e)-[(2e)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine)

SMILES for NP0290021 ((e)-[(2e)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine)

INCHI for NP0290021 ((e)-[(2e)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine)

Structure for NP0290021 ((e)-[(2e)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine)

3D Structure for NP0290021 ((e)-[(2e)-4,6-dibromo-3,7-dimethylocta-2,7-dien-1-ylidene][(2,3,4,5,6-pentafluorophenyl)methoxy]amine)