NP-MRD: Showing NP-Card for 5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene (NP0077855)

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Record Information

Version

2.0

Created at

2022-04-28 23:00:23 UTC

Updated at

2022-04-28 23:00:23 UTC

NP-MRD ID

NP0077855

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene

Description

(1R)-2-(acetyloxy)-1-(5-methylthiophen-2-yl)ethyl acetate belongs to the class of organic compounds known as 2,5-disubstituted thiophenes. These are organic compounds containing a thiophene that is disubstituted at the C-2, and C5-positions. 5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene is found in Xanthopappus subacaulis. Based on a literature review very few articles have been published on (1R)-2-(acetyloxy)-1-(5-methylthiophen-2-yl)ethyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 30 30  0  0  0  0  0  0  0  0999 V2000
    4.7128   -0.0220    0.7612 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3440    0.4825    0.4849 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1310    1.0161   -0.6339 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2963    0.4048    1.3694 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0050    0.8676    1.1397 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3377    0.2085   -0.0444 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2823   -1.1808    0.2207 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8293   -2.1172   -0.6644 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7562   -3.5626   -0.3606 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3666   -1.6493   -1.6980 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1012    0.6562   -0.1483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6643    1.4763   -1.0843 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9723    1.7364   -0.9756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6423    1.1558    0.0708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0913    1.2729    0.4286 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4221    0.2702    0.8617 S   0  0  0  0  0  0  0  0  0  0  0  0
    5.4511    0.5842    0.1903 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9895    0.0519    1.8258 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8451   -1.0712    0.4089 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4050    0.6822    2.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9507    1.9709    0.9613 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8466    0.3685   -0.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2886   -4.0933   -1.1710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2846   -3.9315   -0.3183 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2259   -3.8111    0.6128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0441    1.9053   -1.9024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5428    2.3898   -1.6775 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6057    0.3466    0.1438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2112    1.4171    1.5211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4815    2.1752   -0.0724 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
  6 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 11  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  5 20  1  0
  5 21  1  0
  6 22  1  6
  9 23  1  0
  9 24  1  0
  9 25  1  0
 12 26  1  0
 13 27  1  0
 15 28  1  0
 15 29  1  0
 15 30  1  0
M  END


  Mrv1652304292201002D          

 16 16  0  0  1  0            999 V2000
    0.8545    4.3582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5690    4.7707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1821    4.2187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8465    3.4650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0261    3.5513    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.2590    2.7506    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8465    2.0361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2590    1.3216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0840    1.3216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8465    0.6071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0840    2.7506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4965    2.0361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3215    2.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7340    1.3216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7340    2.7506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1008    4.6938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  1  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
  1 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0077855

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@@H](OC(C)=O)C1=CC=C(C)S1

> <INCHI_IDENTIFIER>
InChI=1S/C11H14O4S/c1-7-4-5-11(16-7)10(15-9(3)13)6-14-8(2)12/h4-5,10H,6H2,1-3H3/t10-/m1/s1

> <INCHI_KEY>
DTHPJWPRPJTZOC-SNVBAGLBSA-N

> <FORMULA>
C11H14O4S

> <MOLECULAR_WEIGHT>
242.29

> <EXACT_MASS>
242.061280105

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
25.05654106153522

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R)-2-(acetyloxy)-1-(5-methylthiophen-2-yl)ethyl acetate

> <ALOGPS_LOGP>
2.19

> <JCHEM_LOGP>
2.016554109666667

> <ALOGPS_LOGS>
-3.10

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.709804234665119

> <JCHEM_POLAR_SURFACE_AREA>
52.6

> <JCHEM_REFRACTIVITY>
59.085600000000014

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.94e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R)-2-(acetyloxy)-1-(5-methylthiophen-2-yl)ethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       1.595   8.135   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.929   8.905   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.073   7.875   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.447   6.468   0.000  0.00  0.00           C+0
HETATM    5  S   UNK     0       1.915   6.629   0.000  0.00  0.00           S+0
HETATM    6  C   UNK     0       4.217   5.134   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       3.447   3.801   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.217   2.467   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.757   2.467   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.447   1.133   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.757   5.134   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       6.527   3.801   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       8.067   3.801   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.837   2.467   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       8.837   5.134   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.188   8.762   0.000  0.00  0.00           C+0
CONECT    1    2    5   16                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4    1                                                       
CONECT    6    4    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    6   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    1                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   32    0
END

View in JSmol

Synonyms

Value	Source
(1R)-2-(Acetyloxy)-1-(5-methylthiophen-2-yl)ethyl acetic acid	Generator

Chemical Formula

C₁₁H₁₄O₄S

Average Mass

242.2900 Da

Monoisotopic Mass

242.06128 Da

IUPAC Name

(1R)-2-(acetyloxy)-1-(5-methylthiophen-2-yl)ethyl acetate

Traditional Name

(1R)-2-(acetyloxy)-1-(5-methylthiophen-2-yl)ethyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@@H](OC(C)=O)C1=CC=C(C)S1

InChI Identifier

InChI=1S/C11H14O4S/c1-7-4-5-11(16-7)10(15-9(3)13)6-14-8(2)12/h4-5,10H,6H2,1-3H3/t10-/m1/s1

InChI Key

DTHPJWPRPJTZOC-SNVBAGLBSA-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
Xanthopappus subacaulis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2,5-disubstituted thiophenes. These are organic compounds containing a thiophene that is disubstituted at the C-2, and C5-positions.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Thiophenes

Sub Class

2,5-disubstituted thiophenes

Direct Parent

2,5-disubstituted thiophenes

Alternative Parents

Substituents

2,5-disubstituted thiophene
Dicarboxylic acid or derivatives
Heteroaromatic compound
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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	2.19	ALOGPS
logP	2.02	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Basic)	-6.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	59.09 m³·mol⁻¹	ChemAxon
Polarizability	25.06 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

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

163103892

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene (NP0077855)

MOL for NP0077855 (5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene)

3D MOL for NP0077855 (5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene)

3D SDF for NP0077855 (5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene)

3D-SDF for NP0077855 (5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene)

PDB for NP0077855 (5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene)

3D PDB for NP0077855 (5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene)

SMILES for NP0077855 (5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene)

INCHI for NP0077855 (5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene)

Structure for NP0077855 (5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene)

3D Structure for NP0077855 (5-(1,2-Diacetoxyethyl)-2-(E)-hept-5-ene-1,3-diynylthiophene)