ChemFOnt: Showing chemical card for 4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid (CFc000155552)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:41:01 UTC

Chemfont ID

CFc000155552

Molecule Identification

Common Name

4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid

Definition

4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid belongs to the class of organic compounds known as bi- and oligothiophenes. These are organic compounds containing two or more linked thiophene rings. Thiophene is a five-member aromatic ring with one sulfur and four carbon atoms. Based on a literature review a significant number of articles have been published on 4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
4-{[2,2'-bithiophene]-5-yl}but-3-ynoate	Generator

Chemical Formula

C₁₂H₈O₂S₂

Average Molecular Weight

248.31

Monoisotopic Molecular Weight

247.996571846

IUPAC Name

4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid

Traditional Name

4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid

CAS Registry Number

Not Available

SMILES

OC(=O)CC#CC1=CC=C(S1)C1=CC=CS1

InChI Identifier

InChI=1S/C12H8O2S2/c13-12(14)5-1-3-9-6-7-11(16-9)10-4-2-8-15-10/h2,4,6-8H,5H2,(H,13,14)

InChI Key

HDRBZACSXVGROU-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bi- and oligothiophenes. These are organic compounds containing two or more linked thiophene rings. Thiophene is a five-member aromatic ring with one sulfur and four carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Bi- and oligothiophenes

Sub Class

Not Available

Direct Parent

Bi- and oligothiophenes

Alternative Parents

Substituents

Bithiophene
2,5-disubstituted thiophene
Heteroaromatic compound
Thiophene
Monocarboxylic acid or derivatives
Carboxylic acid
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

Functional Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.026 g/L	ALOGPS
logP	3.42	ALOGPS
logP	3.42	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	4.13	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	61.7 m³·mol⁻¹	ChemAxon
Polarizability	25.69 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

HMDB0175144

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

98862949

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

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for 4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid (CFc000155552)

MOL for CFc000155552 (4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid)

3D MOL for CFc000155552 (4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid)

3D SDF for CFc000155552 (4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid)

3D-SDF for CFc000155552 (4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid)

PDB for CFc000155552 (4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid)

3D PDB for CFc000155552 (4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid)

SMILES for CFc000155552 (4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid)

INCHI for CFc000155552 (4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid)

Structure for CFc000155552 (4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid)

3D Structure for CFc000155552 (4-{[2,2'-bithiophene]-5-yl}but-3-ynoic acid)