NP-MRD: Showing NP-Card for butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate (NP0249954)

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Record Information

Version

2.0

Created at

2022-09-07 12:39:41 UTC

Updated at

2022-09-07 12:39:41 UTC

NP-MRD ID

NP0249954

Secondary Accession Numbers

None

Natural Product Identification

Common Name

butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate

Description

Butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate belongs to the class of organic compounds known as gamma-keto acids and derivatives. These are organic compounds containing an aldehyde substituted with a keto group on the C4 carbon atom. Butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 39  0  0  0  0  0  0  0  0999 V2000
   -4.4892    1.7154    0.4614 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3477    0.9427   -0.8396 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9227   -0.4402   -0.7239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2229   -1.2450    0.3590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8469   -1.3438    0.0249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0016   -2.0405    0.8640 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4972   -2.5606    1.8994 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5694   -2.1587    0.5367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2713   -1.3809   -0.7051 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1640   -1.5285   -1.0142 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5553   -2.5659   -1.5935 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1118   -0.4806   -0.6494 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8499    0.7166   -0.0136 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0312    1.4193    0.1428 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9885    0.6036   -0.4170 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4579    0.8749   -0.5205 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8672    2.0076    0.3508 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1457   -0.3024   -0.1574 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4195   -0.4768   -0.8601 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8316    2.7212    0.2133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5177    1.7212    0.9727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2679    1.2414    1.1097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2662    0.8470   -1.0890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8836    1.4531   -1.6561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0142   -0.4004   -0.5507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7525   -0.9452   -1.7061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2940   -0.6959    1.3136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7073   -2.2204    0.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0070   -1.6922    1.3681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2533   -3.2254    0.4107 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4989   -0.3087   -0.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9330   -1.6656   -1.5400 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8899    1.0773    0.3208 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1518    2.3908    0.6041 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7700    1.0955   -1.5629 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1979    2.9059   -0.2484 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8001    1.6983    0.9084 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1312    2.3579    1.0719 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8503   -0.1121    0.4838 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  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 19  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 19 12  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  0
  2 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  8 29  1  0
  8 30  1  0
  9 31  1  0
  9 32  1  0
 13 33  1  0
 14 34  1  0
 16 35  1  6
 17 36  1  0
 17 37  1  0
 17 38  1  0
 18 39  1  0
M  END


  Mrv1533004161521512D          

 19 19  0  0  0  0            999 V2000
    2.7964   -3.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5108   -4.3205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2253   -3.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9398   -4.3205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6542   -3.9080    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3687   -4.3205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3687   -5.1455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0832   -3.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7976   -4.3205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5121   -3.9080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5121   -3.0830    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2266   -4.3205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9803   -3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5323   -4.5980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1198   -5.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3128   -5.1410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3528   -4.5118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6883   -3.7581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8377   -5.1792    0.0000 O   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  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 12 16  2  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0249954

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCOC(=O)CCC(=O)C1=CC=C(O1)C(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C14H20O5/c1-3-4-9-18-14(17)8-5-11(16)13-7-6-12(19-13)10(2)15/h6-7,10,15H,3-5,8-9H2,1-2H3

> <INCHI_KEY>
MUODHDJZQZKAKK-UHFFFAOYSA-N

> <FORMULA>
C14H20O5

> <MOLECULAR_WEIGHT>
268.309

> <EXACT_MASS>
268.131073744

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
29.450978509339723

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate

> <ALOGPS_LOGP>
2.00

> <JCHEM_LOGP>
1.4550221773333325

> <ALOGPS_LOGS>
-3.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.711361545835793

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.797716613231685

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0948580180610867

> <JCHEM_POLAR_SURFACE_AREA>
76.74000000000001

> <JCHEM_REFRACTIVITY>
69.4999

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.89e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       5.220  -7.295   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.554  -8.065   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.887  -7.295   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.221  -8.065   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      10.555  -7.295   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      11.888  -8.065   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      11.888  -9.605   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      13.222  -7.295   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.556  -8.065   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      15.889  -7.295   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      15.889  -5.755   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      17.223  -8.065   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      18.630  -7.439   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      19.660  -8.583   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      18.890  -9.917   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      17.384  -9.597   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      21.192  -8.422   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      21.818  -7.015   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      22.097  -9.668   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   16                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15   12                                                       
CONECT   17   14   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   38    0
END

View in JSmol

Synonyms

Value	Source
Butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoic acid	Generator

Chemical Formula

C₁₄H₂₀O₅

Average Mass

268.3090 Da

Monoisotopic Mass

268.13107 Da

IUPAC Name

butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate

Traditional Name

butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate

CAS Registry Number

Not Available

SMILES

CCCCOC(=O)CCC(=O)C1=CC=C(O1)C(C)O

InChI Identifier

InChI=1S/C14H20O5/c1-3-4-9-18-14(17)8-5-11(16)13-7-6-12(19-13)10(2)15/h6-7,10,15H,3-5,8-9H2,1-2H3

InChI Key

MUODHDJZQZKAKK-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as gamma-keto acids and derivatives. These are organic compounds containing an aldehyde substituted with a keto group on the C4 carbon atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Keto acids and derivatives

Sub Class

Gamma-keto acids and derivatives

Direct Parent

Gamma-keto acids and derivatives

Alternative Parents

Substituents

Gamma-keto acid
Aryl ketone
Aryl alkyl ketone
Fatty acid ester
Fatty acyl
Furan
Heteroaromatic compound
Carboxylic acid ester
Ketone
Secondary alcohol
Monocarboxylic acid or derivatives
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Carbonyl group
Organooxygen compound
Organic oxide
Alcohol
Organic oxygen compound
Aromatic alcohol
Hydrocarbon derivative
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	ALOGPS
logP	1.46	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	11.8	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	76.74 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	69.5 m³·mol⁻¹	ChemAxon
Polarizability	29.45 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate (NP0249954)

MOL for NP0249954 (butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate)

3D MOL for NP0249954 (butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate)

3D SDF for NP0249954 (butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate)

3D-SDF for NP0249954 (butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate)

PDB for NP0249954 (butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate)

3D PDB for NP0249954 (butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate)

SMILES for NP0249954 (butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate)

INCHI for NP0249954 (butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate)

Structure for NP0249954 (butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate)

3D Structure for NP0249954 (butyl 4-[5-(1-hydroxyethyl)furan-2-yl]-4-oxobutanoate)