NP-MRD: Showing NP-Card for (2r)-1,1,3,3-tetrabromononan-2-ol (NP0198795)

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Record Information

Version

2.0

Created at

2022-09-04 17:18:26 UTC

Updated at

2022-09-04 17:18:26 UTC

NP-MRD ID

NP0198795

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-1,1,3,3-tetrabromononan-2-ol

Description

(2R)-1,1,3,3-tetrabromononan-2-ol belongs to the class of organic compounds known as bromohydrins. These are alcohols substituted by a bromine atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups. Based on a literature review very few articles have been published on (2R)-1,1,3,3-tetrabromononan-2-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 30 29  0  0  0  0  0  0  0  0999 V2000
   -4.6865   -1.1283    0.0356 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4453   -0.8575   -0.7525 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3485   -0.2698    0.0941 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1551   -0.0387   -0.7933 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0160    0.5604   -0.0135 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1268    0.7329   -1.0289 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3757    1.3196   -0.4283 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9808    3.0661    0.3195 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.6377    1.6010   -1.8595 Br  0  0  0  0  0  0  0  0  0  0  0  0
    2.9989    0.4230    0.6002 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.1537    1.0931    1.0685 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4438   -0.9147    0.0734 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7558   -0.7027   -1.3007 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.2512   -1.9182    1.5274 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -4.4220   -1.2446    1.1233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3859   -0.2762   -0.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1889   -2.0149   -0.3762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6835   -0.1363   -1.5658 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1150   -1.8086   -1.2350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6976    0.7484    0.4205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1290   -0.8615    0.9797 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7719   -0.9751   -1.2476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3779    0.6690   -1.5998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2504    1.5015    0.4721 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3841   -0.1625    0.7666 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7458    1.4979   -1.7648 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2952   -0.1873   -1.5836 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3376    0.2756    1.4866 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5568    1.5057    0.2554 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5976   -1.4973   -0.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  7 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
  1 15  1  0
  1 16  1  0
  1 17  1  0
  2 18  1  0
  2 19  1  0
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  6 26  1  0
  6 27  1  0
 10 28  1  1
 11 29  1  0
 12 30  1  0
M  END

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       1.540  10.669   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.770   9.336   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.540   8.002   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.770   6.668   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.540   5.335   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.770   4.001   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.540   2.667   0.000  0.00  0.00           C+0
HETATM    8 Br   UNK     0       0.206   1.897   0.000  0.00  0.00          Br+0
HETATM    9 Br   UNK     0       2.874   3.437   0.000  0.00  0.00          Br+0
HETATM   10  C   UNK     0       2.310   1.334   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.850   1.334   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM   13 Br   UNK     0       2.310  -1.334   0.000  0.00  0.00          Br+0
HETATM   14 Br   UNK     0       0.000   0.000   0.000  0.00  0.00          Br+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    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   26    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₉H₁₆Br₄O

Average Mass

459.8420 Da

Monoisotopic Mass

455.79347 Da

IUPAC Name

(2R)-1,1,3,3-tetrabromononan-2-ol

Traditional Name

(2R)-1,1,3,3-tetrabromononan-2-ol

CAS Registry Number

Not Available

SMILES

CCCCCCC(Br)(Br)[C@H](O)C(Br)Br

InChI Identifier

InChI=1S/C9H16Br4O/c1-2-3-4-5-6-9(12,13)7(14)8(10)11/h7-8,14H,2-6H2,1H3/t7-/m1/s1

InChI Key

WHZNJMBMGAIYNJ-SSDOTTSWSA-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 bromohydrins. These are alcohols substituted by a bromine atom at a saturated carbon atom otherwise bearing only hydrogen or hydrocarbyl groups.

Kingdom

Organic compounds

Super Class

Organohalogen compounds

Class

Halohydrins

Sub Class

Bromohydrins

Direct Parent

Bromohydrins

Alternative Parents

Substituents

Secondary alcohol
Bromohydrin
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organobromide
Alkyl halide
Alkyl bromide
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	4.15	ChemAxon
pKa (Strongest Acidic)	12.54	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	75.89 m³·mol⁻¹	ChemAxon
Polarizability	31.29 Å³	ChemAxon
Number of Rings	0	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

162894470

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r)-1,1,3,3-tetrabromononan-2-ol (NP0198795)

MOL for NP0198795 ((2r)-1,1,3,3-tetrabromononan-2-ol)

3D MOL for NP0198795 ((2r)-1,1,3,3-tetrabromononan-2-ol)

3D SDF for NP0198795 ((2r)-1,1,3,3-tetrabromononan-2-ol)

3D-SDF for NP0198795 ((2r)-1,1,3,3-tetrabromononan-2-ol)

PDB for NP0198795 ((2r)-1,1,3,3-tetrabromononan-2-ol)

3D PDB for NP0198795 ((2r)-1,1,3,3-tetrabromononan-2-ol)

SMILES for NP0198795 ((2r)-1,1,3,3-tetrabromononan-2-ol)

INCHI for NP0198795 ((2r)-1,1,3,3-tetrabromononan-2-ol)

Structure for NP0198795 ((2r)-1,1,3,3-tetrabromononan-2-ol)

3D Structure for NP0198795 ((2r)-1,1,3,3-tetrabromononan-2-ol)