NP-MRD: Showing NP-Card for [(3e)-3-(chloromethylidene)-6-hydroxy-2h-1-benzoxepin-7-yl]methyl hexadecanoate (NP0314274)

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Record Information

Version

2.0

Created at

2022-09-11 12:17:25 UTC

Updated at

2022-09-11 12:17:25 UTC

NP-MRD ID

NP0314274

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(3e)-3-(chloromethylidene)-6-hydroxy-2h-1-benzoxepin-7-yl]methyl hexadecanoate

Description

{(E)-3-(Chloromethylene)-2,3-dihydrobenzo[b]oxepin-7-yl}methylPalmitate belongs to the class of organic compounds known as benzoxepines. These are organic compounds containing a benzene ring fused to an oxepine ring (an unsaturated seven-membered heterocycle with one oxygen atom replacing a carbon atom). Based on a literature review very few articles have been published on {(E)-3-(Chloromethylene)-2,3-dihydrobenzo[b]oxepin-7-yl}methylPalmitate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112214172D          

 33 34  0  0  0  0            999 V2000
   -9.5008  -10.7686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7863  -10.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0719  -10.7686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3574  -10.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6429  -10.7686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9285  -10.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2140  -10.7686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4995  -10.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7851  -10.7686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0706  -10.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3561  -10.7686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4336  -12.1080    0.0000 O   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
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  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
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 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
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 30 31  1  0  0  0  0
 29 32  1  0  0  0  0
 32 33  1  0  0  0  0
 23 33  1  0  0  0  0
M  END

     RDKit          3D

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    5.5529    0.8179   -0.3322 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5827   -0.5235   -0.0381 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7969   -1.1727    0.2078 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9751   -0.4809    0.1598 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9228    0.8633   -0.1360 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7420    1.5294   -0.3830 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.2785    0.6761   -0.3136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6896   -2.2583    0.4353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1203   -0.9206    1.5112 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.7314   -1.3374    1.5753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3809   -2.1041   -0.8239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7799   -0.4292   -1.3653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4761   -0.8641   -1.4592 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3358   -1.4375    0.1931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1768    1.4147   -0.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
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   12.7045   -0.6181    1.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0487   -1.8368    0.5796 H   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0
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  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
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M  END


  Mrv1652309112214172D          

 33 34  0  0  0  0            999 V2000
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   -8.0719  -10.7686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3574  -10.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6429  -10.7686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9285  -10.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2140  -10.7686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4995  -10.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7851  -10.7686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2127  -10.3561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  5  6  1  0  0  0  0
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M  END
> <DATABASE_ID>
NP0314274

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCC(=O)OCC1=CC=C2OC\C(=C\Cl)C=CC2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C28H41ClO4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-27(30)33-22-24-17-19-26-25(28(24)31)18-16-23(20-29)21-32-26/h16-20,31H,2-15,21-22H2,1H3/b23-20+

> <INCHI_KEY>
ZOPPMWXXWVZRMD-BSYVCWPDSA-N

> <FORMULA>
C28H41ClO4

> <MOLECULAR_WEIGHT>
477.08

> <EXACT_MASS>
476.2693375

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
57.72044586387318

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(3E)-3-(chloromethylidene)-6-hydroxy-2,3-dihydro-1-benzoxepin-7-yl]methyl hexadecanoate

> <JCHEM_LOGP>
8.727995815666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.995013678788894

> <JCHEM_PKA_STRONGEST_BASIC>
-4.885250662050331

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
137.5113

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(3E)-3-(chloromethylidene)-6-hydroxy-2H-1-benzoxepin-7-yl]methyl hexadecanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0     -17.735 -20.101   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -16.401 -19.331   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -15.068 -20.101   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -13.734 -19.331   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -12.400 -20.101   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -11.066 -19.331   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -9.733 -20.101   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -8.399 -19.331   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -7.065 -20.101   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.732 -19.331   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.398 -20.101   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.064 -19.331   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.731 -20.101   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.397 -19.331   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.937 -20.101   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.270 -19.331   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.270 -17.791   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       3.604 -20.101   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.938 -19.331   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.271 -20.101   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.271 -21.641   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.605 -22.411   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.939 -21.641   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.939 -20.101   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.605 -19.331   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.605 -17.791   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      10.143 -19.141   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      11.644 -19.484   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.312 -20.871   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.852 -20.871   0.000  0.00  0.00           C+0
HETATM   31 Cl   UNK     0      14.622 -19.538   0.000  0.00  0.00          Cl+0
HETATM   32  C   UNK     0      11.644 -22.259   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      10.143 -22.602   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   33                                                  
CONECT   24   23   25   27                                                  
CONECT   25   24   20   26                                                  
CONECT   26   25                                                            
CONECT   27   24   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   32                                                  
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   29   33                                                       
CONECT   33   32   23                                                       
MASTER        0    0    0    0    0    0    0    0   33    0   68    0
END

View in JSmol

Synonyms

Value	Source
{(e)-3-(chloromethylene)-2,3-dihydrobenzo[b]oxepin-7-yl}methylpalmitic acid	Generator

Chemical Formula

C₂₈H₄₁ClO₄

Average Mass

477.0800 Da

Monoisotopic Mass

476.26934 Da

IUPAC Name

[(3E)-3-(chloromethylidene)-6-hydroxy-2,3-dihydro-1-benzoxepin-7-yl]methyl hexadecanoate

Traditional Name

[(3E)-3-(chloromethylidene)-6-hydroxy-2H-1-benzoxepin-7-yl]methyl hexadecanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCC(=O)OCC1=CC=C2OC\C(=C\Cl)C=CC2=C1O

InChI Identifier

InChI=1S/C28H41ClO4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-27(30)33-22-24-17-19-26-25(28(24)31)18-16-23(20-29)21-32-26/h16-20,31H,2-15,21-22H2,1H3/b23-20+

InChI Key

ZOPPMWXXWVZRMD-BSYVCWPDSA-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 benzoxepines. These are organic compounds containing a benzene ring fused to an oxepine ring (an unsaturated seven-membered heterocycle with one oxygen atom replacing a carbon atom).

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzoxepines

Sub Class

Not Available

Direct Parent

Benzoxepines

Alternative Parents

Substituents

Benzoxepine
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Fatty acid ester
Fatty acyl
Benzenoid
Carboxylic acid ester
Carboxylic acid derivative
Ether
Oxacycle
Monocarboxylic acid or derivatives
Vinyl chloride
Vinyl halide
Chloroalkene
Haloalkene
Carbonyl group
Organohalogen compound
Organochloride
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
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	8.73	ChemAxon
pKa (Strongest Acidic)	9	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	137.51 m³·mol⁻¹	ChemAxon
Polarizability	57.72 Å³	ChemAxon
Number of Rings	2	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

78434626

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139583552

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(3e)-3-(chloromethylidene)-6-hydroxy-2h-1-benzoxepin-7-yl]methyl hexadecanoate (NP0314274)

MOL for NP0314274 ([(3e)-3-(chloromethylidene)-6-hydroxy-2h-1-benzoxepin-7-yl]methyl hexadecanoate)

3D MOL for NP0314274 ([(3e)-3-(chloromethylidene)-6-hydroxy-2h-1-benzoxepin-7-yl]methyl hexadecanoate)

3D SDF for NP0314274 ([(3e)-3-(chloromethylidene)-6-hydroxy-2h-1-benzoxepin-7-yl]methyl hexadecanoate)

3D-SDF for NP0314274 ([(3e)-3-(chloromethylidene)-6-hydroxy-2h-1-benzoxepin-7-yl]methyl hexadecanoate)

PDB for NP0314274 ([(3e)-3-(chloromethylidene)-6-hydroxy-2h-1-benzoxepin-7-yl]methyl hexadecanoate)

3D PDB for NP0314274 ([(3e)-3-(chloromethylidene)-6-hydroxy-2h-1-benzoxepin-7-yl]methyl hexadecanoate)

SMILES for NP0314274 ([(3e)-3-(chloromethylidene)-6-hydroxy-2h-1-benzoxepin-7-yl]methyl hexadecanoate)

INCHI for NP0314274 ([(3e)-3-(chloromethylidene)-6-hydroxy-2h-1-benzoxepin-7-yl]methyl hexadecanoate)

Structure for NP0314274 ([(3e)-3-(chloromethylidene)-6-hydroxy-2h-1-benzoxepin-7-yl]methyl hexadecanoate)

3D Structure for NP0314274 ([(3e)-3-(chloromethylidene)-6-hydroxy-2h-1-benzoxepin-7-yl]methyl hexadecanoate)