NP-MRD: Showing NP-Card for 8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene (NP0182409)

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Record Information

Version

2.0

Created at

2022-09-03 21:05:32 UTC

Updated at

2022-09-03 21:05:32 UTC

NP-MRD ID

NP0182409

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene

Description

8-Bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]Undeca-1,4-diene belongs to the class of organic compounds known as organochlorides. Organochlorides are compounds containing a chemical bond between a carbon atom and a chlorine atom. 8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene is found in Laurencia translucida. Based on a literature review very few articles have been published on 8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]Undeca-1,4-diene.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
   -0.4396    2.7742   -0.7892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9011    1.3628   -0.7761 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9759    1.1089   -1.5181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5537   -0.2809   -1.5930 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3899   -0.9145   -0.2209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4149   -1.8206    0.2964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3177   -0.6291    0.5105 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1880   -1.2494    1.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2827    0.2769   -0.0331 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5423   -0.5331   -1.0445 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7899   -1.0656   -0.3970 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7078    0.1167   -0.1516 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.9572   -0.3900    0.5375 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2008    0.7536   -1.7390 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    1.9807    1.1589    0.6668 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0215    1.4179    2.3000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.6162    0.7095    1.0880 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4150    2.8647   -1.4794 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1256    3.1469    0.1940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2172    3.4769   -1.1524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4718    1.8802   -2.0917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6479   -0.1497   -1.7047 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1131   -0.8682   -2.3888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0093   -2.8477    0.4966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9513   -1.4441    1.1946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2076   -1.9798   -0.4804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1156   -1.7724    2.1658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0605   -0.4174    2.5855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3018   -1.9101    1.9492 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8078    0.0861   -1.9060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0327   -1.4443   -1.3738 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6071   -1.6083    0.5301 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3083   -1.6881   -1.1742 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7078    0.4484    0.5990 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6906   -0.7637    1.5471 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3711   -1.1890   -0.1114 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0277    2.1047    0.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7796   -0.1950    1.7432 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1865    1.4737    1.7363 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  5  1  0
  5  7  2  0
  7  8  1  0
  9  7  1  1
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  1  6
 12 15  1  0
 15 16  1  0
 15 17  1  0
  9  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
 17  9  1  0
  6 24  1  0
  6 25  1  0
  6 26  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
 10 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 13 34  1  0
 13 35  1  0
 13 36  1  0
 15 37  1  6
 17 38  1  0
 17 39  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
M  END


  Mrv1652309032223052D          

 17 18  0  0  0  0            999 V2000
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8215    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8215   -0.1178    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895   -1.0164    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  2  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
 12 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  9 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0182409

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1=C(C)C2(CCC(C)(Cl)C(Br)C2)C(C)=CC1

> <INCHI_IDENTIFIER>
InChI=1S/C15H22BrCl/c1-10-5-6-11(2)15(12(10)3)8-7-14(4,17)13(16)9-15/h6,13H,5,7-9H2,1-4H3

> <INCHI_KEY>
YHOUJXQBZHXTHW-UHFFFAOYSA-N

> <FORMULA>
C15H22BrCl

> <MOLECULAR_WEIGHT>
317.7

> <EXACT_MASS>
316.059341

> <JCHEM_ACCEPTOR_COUNT>
0

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
31.431789177559097

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene

> <JCHEM_LOGP>
4.844332309333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_POLAR_SURFACE_AREA>
0.0

> <JCHEM_REFRACTIVITY>
80.46439999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene

> <JCHEM_VEBER_RULE>
1

$$$$

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       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.206   3.437   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.954   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.133   1.760   0.000  0.00  0.00           C+0
HETATM   14 Cl   UNK     0       7.133  -0.220   0.000  0.00  0.00          Cl+0
HETATM   15  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   16 Br   UNK     0       5.954  -1.897   0.000  0.00  0.00          Br+0
HETATM   17  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7    2   10   17                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    9                                                       
MASTER        0    0    0    0    0    0    0    0   17    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂BrCl

Average Mass

317.7000 Da

Monoisotopic Mass

316.05934 Da

IUPAC Name

8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene

Traditional Name

8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene

CAS Registry Number

Not Available

SMILES

CC1=C(C)C2(CCC(C)(Cl)C(Br)C2)C(C)=CC1

InChI Identifier

InChI=1S/C15H22BrCl/c1-10-5-6-11(2)15(12(10)3)8-7-14(4,17)13(16)9-15/h6,13H,5,7-9H2,1-4H3

InChI Key

YHOUJXQBZHXTHW-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
Laurencia translucida	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as organochlorides. Organochlorides are compounds containing a chemical bond between a carbon atom and a chlorine atom.

Kingdom

Organic compounds

Super Class

Organohalogen compounds

Class

Organochlorides

Sub Class

Not Available

Direct Parent

Organochlorides

Alternative Parents

Substituents

Hydrocarbon derivative
Organochloride
Organobromide
Alkyl halide
Alkyl chloride
Alkyl bromide
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	4.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	0	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	0 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	80.46 m³·mol⁻¹	ChemAxon
Polarizability	31.43 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

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

163115725

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-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene (NP0182409)

MOL for NP0182409 (8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene)

3D MOL for NP0182409 (8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene)

3D SDF for NP0182409 (8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene)

3D-SDF for NP0182409 (8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene)

PDB for NP0182409 (8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene)

3D PDB for NP0182409 (8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene)

SMILES for NP0182409 (8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene)

INCHI for NP0182409 (8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene)

Structure for NP0182409 (8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene)

3D Structure for NP0182409 (8-bromo-9-chloro-1,2,5,9-tetramethylspiro[5.5]undeca-1,4-diene)