NP-MRD: Showing NP-Card for (3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine (NP0164360)

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Record Information

Version

2.0

Created at

2022-09-02 23:13:36 UTC

Updated at

2022-09-02 23:13:36 UTC

NP-MRD ID

NP0164360

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine

Description

BRASILENYNE belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups. (3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine was first documented in 2002 (PMID: 12487594). Based on a literature review a small amount of articles have been published on BRASILENYNE (PMID: 29255829) (PMID: 15453777).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 36  0  0  0  0  0  0  0  0999 V2000
    6.2410    1.0109   -0.2613 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0626    1.2719   -0.3597 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6742    1.6030   -0.4676 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7934    0.6994   -0.9259 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3664    1.0242   -1.0422 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4945    0.0936   -0.1862 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8042    0.5146   -0.3950 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3913    0.7493    0.8367 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9011    0.7349    0.8084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3691    1.8218   -0.1465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8090   -0.2094    1.8058 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0941   -1.4928    1.7959 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9725   -2.1782    0.8957 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6876   -2.3560   -0.3674 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5457   -1.9690   -1.1481 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6531   -1.3586   -0.5761 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5111   -2.3275    0.6350 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    7.2795    0.7994   -0.1779 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2603    2.5675   -0.1967 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2165   -0.2675   -1.1961 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0154    0.8892   -2.0923 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1993    2.0357   -0.6643 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8873    0.2061    0.8288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1121    1.7819    1.1455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2812    0.9976    1.7970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3610   -0.1917    0.4888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9135    2.7981    0.1094 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0743    1.5986   -1.2006 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4598    1.9270   -0.1279 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1091    0.1987    2.5662 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6036   -2.0528    2.6262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9476   -2.6055    1.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5229   -2.9174   -0.9021 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1674   -2.8234   -1.8188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9452   -1.2659   -1.9611 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4178   -1.3075   -1.4328 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  2  0
  3  2  1  0
  2  1  3  0
  6 16  1  0
 16 17  1  0
 16 15  1  0
 15 14  1  0
 14 13  2  0
 13 12  1  0
 12 11  2  0
 11  8  1  0
 10 27  1  0
 10 28  1  0
 10 29  1  0
  9 25  1  0
  9 26  1  0
  8 24  1  1
  6 23  1  1
  5 21  1  0
  5 22  1  0
  4 20  1  0
  3 19  1  0
  1 18  1  0
 16 36  1  6
 15 34  1  0
 15 35  1  0
 14 33  1  0
 13 32  1  0
 12 31  1  0
 11 30  1  0
M  END


  Mrv1652309032201132D          

 17 17  0  0  0  0            999 V2000
   -1.0101    4.5061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2956    4.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4189    3.6811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4189    2.8561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1333    2.4436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1333    1.6186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9086    1.3364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3211    0.6219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1335    0.7652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4157    1.5404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1778   -0.1905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5458   -0.7208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7208   -0.7208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0888   -0.1905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0544    0.6219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3581    1.3364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1722    1.9684    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
  1  2  3  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
  6 16  1  0  0  0  0
 16 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0164360

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC1OC(C\C=C\C#C)C(Cl)C\C=C/C=C\1

> <INCHI_IDENTIFIER>
InChI=1S/C15H19ClO/c1-3-5-7-12-15-14(16)11-9-6-8-10-13(4-2)17-15/h1,5-10,13-15H,4,11-12H2,2H3/b7-5+,9-6-,10-8-

> <INCHI_KEY>
SMJVVUACAPVPDN-RFVQMCDWSA-N

> <FORMULA>
C15H19ClO

> <MOLECULAR_WEIGHT>
250.77

> <EXACT_MASS>
250.1124429

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
27.943599574599336

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-chloro-9-ethyl-2-[(2E)-pent-2-en-4-yn-1-yl]-2,3,4,9-tetrahydrooxonine

> <ALOGPS_LOGP>
4.86

> <JCHEM_LOGP>
4.063198371333333

> <ALOGPS_LOGS>
-4.82

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.206263471523579

> <JCHEM_POLAR_SURFACE_AREA>
9.23

> <JCHEM_REFRACTIVITY>
76.71600000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.79e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-chloro-9-ethyl-2-[(2E)-pent-2-en-4-yn-1-yl]-2,3,4,9-tetrahydrooxonine

> <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      -1.885   8.411   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.552   7.641   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.782   6.871   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.782   5.331   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.116   4.561   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.116   3.021   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.563   2.495   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.333   1.161   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.849   1.428   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.376   2.875   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.065  -0.356   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.886  -1.346   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.346  -1.346   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.166  -0.356   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.102   1.161   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.668   2.495   0.000  0.00  0.00           C+0
HETATM   17 Cl   UNK     0      -0.321   3.674   0.000  0.00  0.00          Cl+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   16                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15    6   17                                                  
CONECT   17   16                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   34    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₉ClO

Average Mass

250.7700 Da

Monoisotopic Mass

250.11244 Da

IUPAC Name

3-chloro-9-ethyl-2-[(2E)-pent-2-en-4-yn-1-yl]-2,3,4,9-tetrahydrooxonine

Traditional Name

3-chloro-9-ethyl-2-[(2E)-pent-2-en-4-yn-1-yl]-2,3,4,9-tetrahydrooxonine

CAS Registry Number

Not Available

SMILES

CCC1OC(C\C=C\C#C)C(Cl)C\C=C/C=C\1

InChI Identifier

InChI=1S/C15H19ClO/c1-3-5-7-12-15-14(16)11-9-6-8-10-13(4-2)17-15/h1,5-10,13-15H,4,11-12H2,2H3/b7-5+,9-6-,10-8-

InChI Key

SMJVVUACAPVPDN-RFVQMCDWSA-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 dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Ethers

Direct Parent

Dialkyl ethers

Alternative Parents

Substituents

Acetylide
Oxacycle
Organoheterocyclic compound
Dialkyl ether
Hydrocarbon derivative
Organochloride
Organohalogen compound
Alkyl halide
Alkyl chloride
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	4.86	ALOGPS
logP	4.06	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	9.23 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	76.72 m³·mol⁻¹	ChemAxon
Polarizability	27.94 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

5007794

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6511503

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lim C, Ahn J, Sim J, Yun H, Hur J, An H, Jang J, Lee S, Suh YG: Total synthesis of (+)-brasilenyne via concise construction of an oxonane framework containing a 1,3-cis,cis-diene. Chem Commun (Camb). 2018 Jan 11;54(5):467-470. doi: 10.1039/c7cc08329g. [PubMed:29255829 ]
Denmark SE, Yang SM: Total synthesis of (+)-brasilenyne. Application of an intramolecular silicon-assisted cross-coupling reaction. J Am Chem Soc. 2004 Oct 6;126(39):12432-40. doi: 10.1021/ja0466863. [PubMed:15453777 ]
Denmark SE, Yang SM: Intramolecular silicon-assisted cross-coupling: total synthesis of (+)-brasilenyne. J Am Chem Soc. 2002 Dec 25;124(51):15196-7. doi: 10.1021/ja028936q. [PubMed:12487594 ]
LOTUS database [Link]

Showing NP-Card for (3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine (NP0164360)

MOL for NP0164360 ((3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine)

3D MOL for NP0164360 ((3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine)

3D SDF for NP0164360 ((3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine)

3D-SDF for NP0164360 ((3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine)

PDB for NP0164360 ((3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine)

3D PDB for NP0164360 ((3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine)

SMILES for NP0164360 ((3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine)

INCHI for NP0164360 ((3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine)

Structure for NP0164360 ((3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine)

3D Structure for NP0164360 ((3z,5z)-8-chloro-2-ethyl-9-[(2e)-pent-2-en-4-yn-1-yl]-2,7,8,9-tetrahydrooxonine)