NP-MRD: Showing NP-Card for 4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane (NP0057327)

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Record Information

Version

2.0

Created at

2022-04-28 02:47:50 UTC

Updated at

2022-04-28 02:47:50 UTC

NP-MRD ID

NP0057327

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane

Description

(2S)-2-[(2S,3R,5R)-3,6-dibromo-2,5-dichloro-6-methylheptan-2-yl]oxirane belongs to the class of organic compounds known as epoxides. Epoxides are compounds containing a cyclic ether with three ring atoms(one oxygen and two carbon atoms). 4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane is found in Plocamium cartilagineum. Based on a literature review very few articles have been published on (2S)-2-[(2S,3R,5R)-3,6-dibromo-2,5-dichloro-6-methylheptan-2-yl]oxirane.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 31 31  0  0  0  0  0  0  0  0999 V2000
    2.4114    1.6910   -0.4305 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7035    0.3545    0.1829 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4593   -0.5543   -0.7471 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8256    0.6324    1.7555 Br  0  0  0  0  0  0  0  0  0  0  0  0
    1.4196   -0.3150    0.7026 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8695   -1.8569    1.3933 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.4240   -0.3838   -0.3991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8845   -0.9988   -0.1136 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7671   -2.8382    0.4605 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -1.8093   -0.2652    0.7945 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0725   -1.1496    0.8947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2143   -0.0740    2.4437 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   -2.3118    1.0514    0.2546 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1011    1.0023   -1.0480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8576    1.5701   -0.9326 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5026    2.1637   -0.0154 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2208    1.5510   -1.5275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2712    2.3858   -0.3489 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4114   -0.9405   -0.2895 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8780   -1.3988   -1.1242 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8051    0.0316   -1.6428 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0813    0.3784    1.5152 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2600    0.6540   -0.7687 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8953   -0.9401   -1.2603 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4267   -1.0492   -1.1092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8524   -2.0648    1.4745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9086   -0.5682    1.3225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3627   -1.4825   -0.1251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7266    1.7466    1.0111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1345    0.0614   -1.6177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0089    1.6058   -1.1158 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  1
  2  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  1
 10 13  1  0
 13 14  1  0
 14 15  1  0
 15 13  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  3 19  1  0
  3 20  1  0
  3 21  1  0
  5 22  1  1
  7 23  1  0
  7 24  1  0
  8 25  1  6
 11 26  1  0
 11 27  1  0
 11 28  1  0
 13 29  1  1
 14 30  1  0
 14 31  1  0
M  END


  Mrv1652304282204472D          

 15 15  0  0  1  0            999 V2000
   -0.4763    2.9513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2382    2.5388    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2382    1.7138    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5868    1.7138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2382    0.8888    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6507    0.1743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1743    0.1743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0632    1.7138    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    0.9526    2.9513    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -0.4763    3.7763    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1908    4.1888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9053    4.6013    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -0.7783    4.9033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6033    3.4743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2382    4.1888    0.0000 Cl  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  6  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  5  7  1  0  0  0  0
  3  8  1  6  0  0  0
  2  9  1  1  0  0  0
  1 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 11 14  1  0  0  0  0
 10 15  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0057327

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(Br)[C@H](Cl)C[C@@H](Br)[C@@](C)(Cl)[C@@H]1CO1

> <INCHI_IDENTIFIER>
InChI=1S/C10H16Br2Cl2O/c1-9(2,12)7(13)4-6(11)10(3,14)8-5-15-8/h6-8H,4-5H2,1-3H3/t6-,7-,8+,10-/m1/s1

> <INCHI_KEY>
HGUFNQRFLLYYNW-BDNRQGISSA-N

> <FORMULA>
C10H16Br2Cl2O

> <MOLECULAR_WEIGHT>
382.95

> <EXACT_MASS>
379.894497

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
29.15794887702176

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-[(2S,3R,5R)-3,6-dibromo-2,5-dichloro-6-methylheptan-2-yl]oxirane

> <ALOGPS_LOGP>
5.13

> <JCHEM_LOGP>
4.258730773333333

> <ALOGPS_LOGS>
-6.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.191762841469813

> <JCHEM_POLAR_SURFACE_AREA>
12.53

> <JCHEM_REFRACTIVITY>
71.6251

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.62e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(2S,3R,5R)-3,6-dibromo-2,5-dichloro-6-methylheptan-2-yl]oxirane

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -0.889   5.509   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.445   4.739   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.445   3.199   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.095   3.199   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.445   1.659   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.215   0.325   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.325   0.325   0.000  0.00  0.00           O+0
HETATM    8 Cl   UNK     0       1.985   3.199   0.000  0.00  0.00          Cl+0
HETATM    9 Br   UNK     0       1.778   5.509   0.000  0.00  0.00          Br+0
HETATM   10  C   UNK     0      -0.889   7.049   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.223   7.819   0.000  0.00  0.00           C+0
HETATM   12 Br   UNK     0      -3.556   8.589   0.000  0.00  0.00          Br+0
HETATM   13  C   UNK     0      -1.453   9.153   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.993   6.485   0.000  0.00  0.00           C+0
HETATM   15 Cl   UNK     0       0.445   7.819   0.000  0.00  0.00          Cl+0
CONECT    1    2   10                                                       
CONECT    2    1    3    9                                                  
CONECT    3    2    4    5    8                                             
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5    7                                                       
CONECT    7    6    5                                                       
CONECT    8    3                                                            
CONECT    9    2                                                            
CONECT   10    1   11   15                                                  
CONECT   11   10   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11                                                            
CONECT   15   10                                                            
MASTER        0    0    0    0    0    0    0    0   15    0   30    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₀H₁₆Br₂Cl₂O

Average Mass

382.9500 Da

Monoisotopic Mass

379.89450 Da

IUPAC Name

(2S)-2-[(2S,3R,5R)-3,6-dibromo-2,5-dichloro-6-methylheptan-2-yl]oxirane

Traditional Name

(2S)-2-[(2S,3R,5R)-3,6-dibromo-2,5-dichloro-6-methylheptan-2-yl]oxirane

CAS Registry Number

Not Available

SMILES

CC(C)(Br)[C@H](Cl)C[C@@H](Br)[C@@](C)(Cl)[C@@H]1CO1

InChI Identifier

InChI=1S/C10H16Br2Cl2O/c1-9(2,12)7(13)4-6(11)10(3,14)8-5-15-8/h6-8H,4-5H2,1-3H3/t6-,7-,8+,10-/m1/s1

InChI Key

HGUFNQRFLLYYNW-BDNRQGISSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Plocamium cartilagineum	-	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as epoxides. Epoxides are compounds containing a cyclic ether with three ring atoms(one oxygen and two carbon atoms).

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Epoxides

Sub Class

Not Available

Direct Parent

Epoxides

Alternative Parents

Substituents

Oxacycle
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organochloride
Organobromide
Organohalogen compound
Alkyl halide
Alkyl chloride
Alkyl bromide
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic 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	5.13	ALOGPS
logP	4.26	ChemAxon
logS	-6.2	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	12.53 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	71.63 m³·mol⁻¹	ChemAxon
Polarizability	29.16 Å³	ChemAxon
Number of Rings	1	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

163042008

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane (NP0057327)

MOL for NP0057327 (4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane)

3D MOL for NP0057327 (4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane)

3D SDF for NP0057327 (4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane)

3D-SDF for NP0057327 (4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane)

PDB for NP0057327 (4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane)

3D PDB for NP0057327 (4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane)

SMILES for NP0057327 (4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane)

INCHI for NP0057327 (4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane)

Structure for NP0057327 (4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane)

3D Structure for NP0057327 (4,7-Dibromo-3,6-dichloro-3,7-dimethyl-1,2-epoxyoctane)