NP-MRD: Showing NP-Card for (5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol (NP0195204)

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Record Information

Version

2.0

Created at

2022-09-04 13:01:21 UTC

Updated at

2022-09-04 13:01:21 UTC

NP-MRD ID

NP0195204

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol

Description

(5R)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. (5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol is found in Arabis hirsuta. Based on a literature review very few articles have been published on (5R)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042215012D          

 14 15  0  0  1  0            999 V2000
   -0.0000    7.1786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    6.7661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    5.9411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    5.5286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.2911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.4661    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3819    2.9812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    2.1965    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    2.1965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1830    1.5291    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470    2.9812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    5.5286    0.0000 C   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
  7 12  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  2  0  0  0  0
  3 14  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0195204

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1)[C@@H]1CN=C(S)O1

> <INCHI_IDENTIFIER>
InChI=1S/C10H11NO2S/c1-12-8-4-2-7(3-5-8)9-6-11-10(14)13-9/h2-5,9H,6H2,1H3,(H,11,14)/t9-/m0/s1

> <INCHI_KEY>
ZINZVEYXHGBFCB-VIFPVBQESA-N

> <FORMULA>
C10H11NO2S

> <MOLECULAR_WEIGHT>
209.26

> <EXACT_MASS>
209.051049772

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
25

> <JCHEM_AVERAGE_POLARIZABILITY>
21.847891467832554

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5R)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol

> <JCHEM_LOGP>
2.5677746653333338

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.681317966470004

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.558201353462313

> <JCHEM_PKA_STRONGEST_BASIC>
2.445083788404811

> <JCHEM_POLAR_SURFACE_AREA>
30.82

> <JCHEM_REFRACTIVITY>
56.680800000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(5R)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol

> <JCHEM_VEBER_RULE>
1

$$$$

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      -0.000  13.400   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.334  12.630   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.334  11.090   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  10.320   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   8.780   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334   8.010   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   6.470   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.580   5.565   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       2.104   4.100   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       0.564   4.100   0.000  0.00  0.00           C+0
HETATM   11  S   UNK     0      -0.342   2.854   0.000  0.00  0.00           S+0
HETATM   12  O   UNK     0       0.088   5.565   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.000   8.780   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.000  10.320   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   14                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   13                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    7                                                       
CONECT   13    6   14                                                       
CONECT   14   13    3                                                       
MASTER        0    0    0    0    0    0    0    0   14    0   30    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₀H₁₁NO₂S

Average Mass

209.2600 Da

Monoisotopic Mass

209.05105 Da

IUPAC Name

(5R)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol

Traditional Name

(5R)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)[C@@H]1CN=C(S)O1

InChI Identifier

InChI=1S/C10H11NO2S/c1-12-8-4-2-7(3-5-8)9-6-11-10(14)13-9/h2-5,9H,6H2,1H3,(H,11,14)/t9-/m0/s1

InChI Key

ZINZVEYXHGBFCB-VIFPVBQESA-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
Arabis hirsuta	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Phenoxy compound
Anisole
Methoxybenzene
Alkyl aryl ether
Monocyclic benzene moiety
Oxazoline
Ether
Oxacycle
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic nitrogen compound
Organosulfur compound
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organopnictogen compound
Organic oxygen compound
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	2.57	ChemAxon
pKa (Strongest Acidic)	6.56	ChemAxon
pKa (Strongest Basic)	2.45	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	30.82 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	56.68 m³·mol⁻¹	ChemAxon
Polarizability	21.85 Å³	ChemAxon
Number of Rings	2	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

163032364

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol (NP0195204)

MOL for NP0195204 ((5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol)

3D MOL for NP0195204 ((5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol)

3D SDF for NP0195204 ((5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol)

3D-SDF for NP0195204 ((5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol)

PDB for NP0195204 ((5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol)

3D PDB for NP0195204 ((5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol)

SMILES for NP0195204 ((5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol)

INCHI for NP0195204 ((5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol)

Structure for NP0195204 ((5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol)

3D Structure for NP0195204 ((5r)-5-(4-methoxyphenyl)-4,5-dihydro-1,3-oxazole-2-thiol)