NP-MRD: Showing NP-Card for 1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate (NP0176490)

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Record Information

Version

2.0

Created at

2022-09-03 14:09:40 UTC

Updated at

2022-09-03 14:09:41 UTC

NP-MRD ID

NP0176490

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate

Description

1,3-Ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate belongs to the class of organic compounds known as phenoxy compounds. These are aromatic compounds contaning a phenoxy group. 1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate is found in Cynodon dactylon. Based on a literature review very few articles have been published on 1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032216092D          

 40 42  0  0  0  0            999 V2000
    0.0000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 Si  0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 O   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 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
    1.2978   -1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1228   -1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5353   -1.1064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3603   -1.1064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7728   -1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5978   -1.8209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0103   -2.5353    0.0000 Si  0  0  0  0  0  0  0  0  0  0  0  0
    5.4228   -3.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7248   -2.1228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2959   -2.9478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4289   -4.4667    0.0000 Si  0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -4.4667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5814   -2.5353    0.0000 Si  0  0  0  0  0  0  0  0  0  0  0  0
   -3.9939   -3.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9314   -1.1064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1064   -1.1064    0.0000 C   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
  2  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 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
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 13 19  1  0  0  0  0
 19 20  2  0  0  0  0
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  9 21  1  0  0  0  0
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 21 29  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  1  0  0  0  0
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 31 32  1  0  0  0  0
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 35 37  1  0  0  0  0
 35 38  1  0  0  0  0
 33 39  1  0  0  0  0
 39 40  2  0  0  0  0
 30 40  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309032216092D          

 40 42  0  0  0  0            999 V2000
    0.0000    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2959   -2.9478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3603   -2.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5353   -2.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.4042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.2292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.6417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.6417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.4667    0.0000 Si  0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -4.4667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -4.4667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -5.2917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1311   -1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6939   -1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1064   -2.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9314   -2.5353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3439   -1.8209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1689   -1.8209    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5814   -2.5353    0.0000 Si  0  0  0  0  0  0  0  0  0  0  0  0
   -3.9939   -3.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2959   -2.1228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8669   -2.9478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9314   -1.1064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1064   -1.1064    0.0000 C   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
  2  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 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
 15 17  1  0  0  0  0
 15 18  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  2  0  0  0  0
 10 20  1  0  0  0  0
  9 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 21 29  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 35 38  1  0  0  0  0
 33 39  1  0  0  0  0
 39 40  2  0  0  0  0
 30 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0176490

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[Si](C)(C)OC(=O)C1C(C(C1C1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C)C1=CC=C(O[Si](C)(C)C)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C30H48O6Si4/c1-37(2,3)33-23-17-13-21(14-18-23)25-27(29(31)35-39(7,8)9)26(28(25)30(32)36-40(10,11)12)22-15-19-24(20-16-22)34-38(4,5)6/h13-20,25-28H,1-12H3

> <INCHI_KEY>
LKRSQFNXURZKDX-UHFFFAOYSA-N

> <FORMULA>
C30H48O6Si4

> <MOLECULAR_WEIGHT>
617.048

> <EXACT_MASS>
616.252795406

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
66.49121689661773

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate

> <JCHEM_LOGP>
8.729399999999998

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.383403385182238

> <JCHEM_POLAR_SURFACE_AREA>
71.06

> <JCHEM_REFRACTIVITY>
149.20999999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000   3.080   0.000  0.00  0.00           C+0
HETATM    2 Si   UNK     0       0.000   1.540   0.000  0.00  0.00          Si+0
HETATM    3  C   UNK     0       1.540   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.540   1.540   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667  -0.000   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       2.423  -3.399   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.963  -3.399   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.733  -2.065   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.273  -2.065   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.043  -3.399   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.583  -3.399   0.000  0.00  0.00           O+0
HETATM   15 Si   UNK     0       9.353  -4.733   0.000  0.00  0.00          Si+0
HETATM   16  C   UNK     0      10.123  -6.066   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.686  -3.963   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.019  -5.503   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.273  -4.733   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.733  -4.733   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.334  -4.488   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334  -6.028   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.000  -6.798   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       2.667  -6.798   0.000  0.00  0.00           O+0
HETATM   25 Si   UNK     0       2.667  -8.338   0.000  0.00  0.00          Si+0
HETATM   26  C   UNK     0       1.127  -8.338   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.207  -8.338   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.667  -9.878   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.245  -3.399   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.295  -3.399   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.065  -4.733   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -3.605  -4.733   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -4.375  -3.399   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -5.915  -3.399   0.000  0.00  0.00           O+0
HETATM   35 Si   UNK     0      -6.685  -4.733   0.000  0.00  0.00          Si+0
HETATM   36  C   UNK     0      -7.455  -6.066   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -8.019  -3.963   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -5.352  -5.503   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -3.605  -2.065   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -2.065  -2.065   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   29                                                  
CONECT    9    8   10   21                                                  
CONECT   10    9   11   20                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17   18                                             
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   15                                                            
CONECT   19   13   20                                                       
CONECT   20   19   10                                                       
CONECT   21    9   22   29                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25                                                            
CONECT   29   21    8   30                                                  
CONECT   30   29   31   40                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   39                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37   38                                             
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   35                                                            
CONECT   39   33   40                                                       
CONECT   40   39   30                                                       
MASTER        0    0    0    0    0    0    0    0   40    0   84    0
END

View in JSmol

Synonyms

Value	Source
1,3-Ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylic acid	Generator

Chemical Formula

C₃₀H₄₈O₆Si₄

Average Mass

617.0480 Da

Monoisotopic Mass

616.25280 Da

IUPAC Name

1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate

Traditional Name

1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate

CAS Registry Number

Not Available

SMILES

C[Si](C)(C)OC(=O)C1C(C(C1C1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C)C1=CC=C(O[Si](C)(C)C)C=C1

InChI Identifier

InChI=1S/C30H48O6Si4/c1-37(2,3)33-23-17-13-21(14-18-23)25-27(29(31)35-39(7,8)9)26(28(25)30(32)36-40(10,11)12)22-15-19-24(20-16-22)34-38(4,5)6/h13-20,25-28H,1-12H3

InChI Key

LKRSQFNXURZKDX-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
Cynodon dactylon	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenoxy compounds. These are aromatic compounds contaning a phenoxy group.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Phenoxy compounds

Direct Parent

Phenoxy compounds

Alternative Parents

Substituents

Phenoxy compound
Trimethylsilyl ester
Dicarboxylic acid or derivatives
Trialkylheterosilane
Carboxylic acid salt
Organoheterosilane
Organic metalloid salt
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Organic salt
Organosilicon compound
Organooxygen compound
Organic oxygen compound
Carbonyl group
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	8.73	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	71.06 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	149.21 m³·mol⁻¹	ChemAxon
Polarizability	66.49 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	Yes	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

13989541

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate (NP0176490)

MOL for NP0176490 (1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate)

3D MOL for NP0176490 (1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate)

3D SDF for NP0176490 (1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate)

3D-SDF for NP0176490 (1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate)

PDB for NP0176490 (1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate)

3D PDB for NP0176490 (1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate)

SMILES for NP0176490 (1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate)

INCHI for NP0176490 (1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate)

Structure for NP0176490 (1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate)

3D Structure for NP0176490 (1,3-ditrimethylsilyl 2,4-bis({4-[(trimethylsilyl)oxy]phenyl})cyclobutane-1,3-dicarboxylate)