NP-MRD: Showing NP-Card for 3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate (NP0294800)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 03:30:29 UTC

Updated at

2022-09-10 03:30:29 UTC

NP-MRD ID

NP0294800

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate

Description

AC1L7RIK belongs to the class of organic compounds known as cinnamic acid esters. These are compound containing an ester derivative of cinnamic acid. 3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate is found in Cinnamomum triplinerve. AC1L7RIK is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 32 32  0  0  0  0  0  0  0  0999 V2000
    6.2278   -0.8234   -0.3496 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5547   -0.4713   -0.7745 S   0  0  0  0  0  6  0  0  0  0  0  0
    3.8354   -1.6510   -1.3432 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4919    0.6318   -1.8197 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6278    0.0767    0.6259 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9058    1.1833    0.5840 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1376    1.6181    1.7768 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7747    1.6611    1.3954 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0919    0.5561    0.9402 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6833   -0.5401    0.8532 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2905    0.6662    0.5689 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9429   -0.3851    0.1351 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3419   -0.3897   -0.2678 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1166    0.7553   -0.2221 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4562    0.7140   -0.6166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0086   -0.4615   -1.0507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2545   -1.6155   -1.1044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9354   -1.5510   -0.7104 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8746   -0.4913   -1.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5600   -0.3440    0.5872 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4124   -1.9335   -0.2875 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6515   -0.5046    1.5355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8745    1.7763   -0.3263 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4905    2.6018    2.1282 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2229    0.8477    2.5551 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7780    1.6205    0.6526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3995   -1.3301    0.0697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7191    1.7011    0.1136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0853    1.5991   -0.5899 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0486   -0.5053   -1.3597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7109   -2.5535   -1.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3293   -2.4582   -0.7488 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  2  0
  2  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 13  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  5 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
 11 26  1  0
 12 27  1  0
 14 28  1  0
 15 29  1  0
 16 30  1  0
 17 31  1  0
 18 32  1  0
M  END


  Mrv1533004161505362D          

 18 18  0  0  0  0            999 V2000
   -2.8579    6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    6.1875    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559    5.4730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7309    6.9020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  2  0  0  0  0
  5  2  1  4  0  0  0
  5  6  2  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  2  0  0  0  0
 11  9  1  4  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  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0294800

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CS(=O)(=O)C=CCOC(=O)C=CC1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C13H14O4S/c1-18(15,16)11-5-10-17-13(14)9-8-12-6-3-2-4-7-12/h2-9,11H,10H2,1H3

> <INCHI_KEY>
XKWYWPLJJOFUCZ-UHFFFAOYSA-N

> <FORMULA>
C13H14O4S

> <MOLECULAR_WEIGHT>
266.31

> <EXACT_MASS>
266.061280105

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
27.17754664512382

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate

> <ALOGPS_LOGP>
2.15

> <JCHEM_LOGP>
1.571130685

> <ALOGPS_LOGS>
-4.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.818253723576805

> <JCHEM_POLAR_SURFACE_AREA>
60.440000000000005

> <JCHEM_REFRACTIVITY>
71.08550000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.92e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate

> <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      -5.335  12.320   0.000  0.00  0.00           C+0
HETATM    2  S   UNK     0      -4.001  11.550   0.000  0.00  0.00           S+0
HETATM    3  O   UNK     0      -4.771  10.216   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -3.231  12.884   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -2.667  10.780   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.667   9.240   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -1.334   6.930   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.334   6.930   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   13                                                       
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₁₄O₄S

Average Mass

266.3100 Da

Monoisotopic Mass

266.06128 Da

IUPAC Name

3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate

Traditional Name

3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate

CAS Registry Number

Not Available

SMILES

CS(=O)(=O)C=CCOC(=O)C=CC1=CC=CC=C1

InChI Identifier

InChI=1S/C13H14O4S/c1-18(15,16)11-5-10-17-13(14)9-8-12-6-3-2-4-7-12/h2-9,11H,10H2,1H3

InChI Key

XKWYWPLJJOFUCZ-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

Species Name	Source	Reference
Cinnamomum triplinerve	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cinnamic acid esters. These are compound containing an ester derivative of cinnamic acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Cinnamic acid esters

Direct Parent

Cinnamic acid esters

Alternative Parents

Substituents

Cinnamic acid ester
Styrene
Fatty acid ester
Monocyclic benzene moiety
Benzenoid
Fatty acyl
Enoate ester
Sulfonyl
Sulfone
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organosulfur compound
Organooxygen compound
Organic oxygen compound
Carbonyl group
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	2.15	ALOGPS
logP	1.57	ChemAxon
logS	-4.1	ALOGPS
pKa (Strongest Basic)	-6.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	60.44 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	71.09 m³·mol⁻¹	ChemAxon
Polarizability	27.18 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

340125

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate (NP0294800)

MOL for NP0294800 (3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate)

3D MOL for NP0294800 (3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate)

3D SDF for NP0294800 (3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate)

3D-SDF for NP0294800 (3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate)

PDB for NP0294800 (3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate)

3D PDB for NP0294800 (3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate)

SMILES for NP0294800 (3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate)

INCHI for NP0294800 (3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate)

Structure for NP0294800 (3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate)

3D Structure for NP0294800 (3-methanesulfonylprop-2-en-1-yl 3-phenylprop-2-enoate)