NP-MRD: Showing NP-Card for (5r)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one (NP0289445)

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Record Information

Version

2.0

Created at

2022-09-09 19:38:26 UTC

Updated at

2022-09-09 19:38:26 UTC

NP-MRD ID

NP0289445

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5r)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one

Description

(5R)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxy-2,5-dihydrofuran-2-one belongs to the class of organic compounds known as o-bromophenols. These are bromophenols carrying a iodine at the C2 position of the benzene ring. Based on a literature review very few articles have been published on (5R)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxy-2,5-dihydrofuran-2-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092221382D          

 26 28  0  0  1  0            999 V2000
    3.0128   -2.7393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5279   -2.0718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7029   -2.0718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4480   -1.2872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6633   -1.0323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0502   -1.5843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7344   -1.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3475   -1.8814    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -0.9059   -0.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6905   -0.2675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2928    0.0296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4643    0.8366    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.4918   -0.2253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1154   -0.8023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5634   -0.1892    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6674   -0.1892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4744   -0.3607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0264    0.2524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8334    0.0808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3854    0.6939    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    5.0883   -0.7038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8953   -0.8753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5363   -1.3169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7912   -2.1015    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.7293   -1.1454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7828   -1.2872    0.0000 O   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
  3  4  2  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  0  0  0  0
  7  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  5 13  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 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
 17 25  1  0  0  0  0
 14 26  1  0  0  0  0
  2 26  1  0  0  0  0
M  END

     RDKit          3D

 36 38  0  0  0  0  0  0  0  0999 V2000
    0.7645   -0.0394    4.4500 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3691   -0.1956    3.2512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0039   -0.1913    2.7746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0129   -0.3794    1.4669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2603   -0.4370    0.6761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4933   -0.2095    1.2437 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6753   -0.2863    0.5005 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3705    0.0317    1.3034 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -4.6296   -0.5966   -0.8379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8121   -0.6741   -1.5855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3982   -0.8240   -1.4040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3472   -1.2534   -3.2607 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -2.2103   -0.7480   -0.6613 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3682   -0.5079    1.0158 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5916   -1.6641    0.2709 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7012    0.7372    0.1890 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1002    0.7636   -0.2569 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1141    1.3524    0.5058 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4111    1.3496    0.0405 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7784    2.1596    1.0998 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.7325    0.7818   -1.1558 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0387    0.8053   -1.5743 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7219    0.1983   -1.9096 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1986   -0.5959   -3.5924 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.4151    0.1900   -1.4620 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1612   -0.4008    2.1602 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8942   -0.0524    3.4119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5553    0.0338    2.2814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7149   -0.5061   -1.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2786   -0.9467   -1.1460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1209   -2.3533    0.4171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0487    0.9293   -0.5833 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5943    1.6104    0.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8411    1.8005    1.4568 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2792    0.3888   -2.4533 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6450   -0.2704   -2.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21 19  2  0
 19 20  1  0
 19 18  1  0
 18 17  2  0
 17 16  1  0
 16 14  1  0
 14 15  1  6
 14 26  1  0
 26  2  1  0
  2  1  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 11 13  2  0
 17 25  1  0
 25 23  2  0
 23 24  1  0
 23 21  1  0
  4 14  1  0
 13  5  1  0
 22 35  1  0
 18 34  1  0
 16 32  1  0
 16 33  1  0
 15 31  1  0
  3 27  1  0
  6 28  1  0
 10 29  1  0
 13 30  1  0
 25 36  1  0
M  END


  Mrv1652309092221382D          

 26 28  0  0  1  0            999 V2000
    3.0128   -2.7393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5279   -2.0718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7029   -2.0718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4480   -1.2872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6633   -1.0323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0502   -1.5843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7344   -1.3294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3475   -1.8814    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -0.9059   -0.5224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6905   -0.2675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2928    0.0296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4643    0.8366    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.4918   -0.2253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1154   -0.8023    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5634   -0.1892    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6674   -0.1892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4744   -0.3607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0264    0.2524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8334    0.0808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3854    0.6939    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    5.0883   -0.7038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8953   -0.8753    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5363   -1.3169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7912   -2.1015    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.7293   -1.1454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7828   -1.2872    0.0000 O   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
  3  4  2  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  0  0  0  0
  7  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  5 13  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 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
 17 25  1  0  0  0  0
 14 26  1  0  0  0  0
  2 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0289445

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=C(Br)C=C(C[C@@]2(O)OC(=O)C=C2C2=CC(Br)=C(O)C(Br)=C2)C=C1Br

> <INCHI_IDENTIFIER>
InChI=1S/C17H10Br4O5/c18-10-1-7(2-11(19)15(10)23)6-17(25)9(5-14(22)26-17)8-3-12(20)16(24)13(21)4-8/h1-5,23-25H,6H2/t17-/m1/s1

> <INCHI_KEY>
FOTKCGFQUISHNJ-QGZVFWFLSA-N

> <FORMULA>
C17H10Br4O5

> <MOLECULAR_WEIGHT>
613.878

> <EXACT_MASS>
609.726175

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
43.82704899202924

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5R)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxy-2,5-dihydrofuran-2-one

> <JCHEM_LOGP>
6.174909909

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
6.933796511533768

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.284885603478095

> <JCHEM_PKA_STRONGEST_BASIC>
-4.508998370672537

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
110.6929

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(5R)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

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  O   UNK     0       5.624  -5.113   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.719  -3.867   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.179  -3.867   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.703  -2.403   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.238  -1.927   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.094  -2.957   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.371  -2.482   0.000  0.00  0.00           C+0
HETATM    8 Br   UNK     0      -2.515  -3.512   0.000  0.00  0.00          Br+0
HETATM    9  C   UNK     0      -1.691  -0.975   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -3.156  -0.499   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -0.547   0.055   0.000  0.00  0.00           C+0
HETATM   12 Br   UNK     0      -0.867   1.562   0.000  0.00  0.00          Br+0
HETATM   13  C   UNK     0       0.918  -0.421   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.949  -1.498   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.918  -0.353   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.979  -0.353   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.486  -0.673   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.516   0.471   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.022   0.151   0.000  0.00  0.00           C+0
HETATM   20 Br   UNK     0      10.053   1.295   0.000  0.00  0.00          Br+0
HETATM   21  C   UNK     0       9.498  -1.314   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      11.005  -1.634   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       8.468  -2.458   0.000  0.00  0.00           C+0
HETATM   24 Br   UNK     0       8.944  -3.923   0.000  0.00  0.00          Br+0
HETATM   25  C   UNK     0       6.961  -2.138   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.195  -2.403   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   26                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   14                                                  
CONECT    5    4    6   13                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11    5                                                       
CONECT   14    4   15   16   26                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   17                                                       
CONECT   26   14    2                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₀Br₄O₅

Average Mass

613.8780 Da

Monoisotopic Mass

609.72618 Da

IUPAC Name

(5R)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxy-2,5-dihydrofuran-2-one

Traditional Name

(5R)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one

CAS Registry Number

Not Available

SMILES

OC1=C(Br)C=C(C[C@@]2(O)OC(=O)C=C2C2=CC(Br)=C(O)C(Br)=C2)C=C1Br

InChI Identifier

InChI=1S/C17H10Br4O5/c18-10-1-7(2-11(19)15(10)23)6-17(25)9(5-14(22)26-17)8-3-12(20)16(24)13(21)4-8/h1-5,23-25H,6H2/t17-/m1/s1

InChI Key

FOTKCGFQUISHNJ-QGZVFWFLSA-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 o-bromophenols. These are bromophenols carrying a iodine at the C2 position of the benzene ring.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

2-bromophenol
Bromobenzene
Halobenzene
Aryl bromide
Aryl halide
Monocyclic benzene moiety
2-furanone
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Dihydrofuran
Carboxylic acid ester
Hemiacetal
Lactone
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Monocarboxylic acid or derivatives
Organic oxygen compound
Organobromide
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organohalogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	6.17	ChemAxon
pKa (Strongest Acidic)	6.28	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	110.69 m³·mol⁻¹	ChemAxon
Polarizability	43.83 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

163048130

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5r)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one (NP0289445)

MOL for NP0289445 ((5r)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one)

3D MOL for NP0289445 ((5r)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one)

3D SDF for NP0289445 ((5r)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one)

3D-SDF for NP0289445 ((5r)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one)

PDB for NP0289445 ((5r)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one)

3D PDB for NP0289445 ((5r)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one)

SMILES for NP0289445 ((5r)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one)

INCHI for NP0289445 ((5r)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one)

Structure for NP0289445 ((5r)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one)

3D Structure for NP0289445 ((5r)-4-(3,5-dibromo-4-hydroxyphenyl)-5-[(3,5-dibromo-4-hydroxyphenyl)methyl]-5-hydroxyfuran-2-one)