POLY(THIOPHENE-2,5-DIYL), BR TERMINATED

Product Information

Molecular Formula:
C4H4S
Molecular Weight:
84.13960
Description
Thiophene appears as a colorless liquid with an unpleasant odor. Insoluble in water and slightly denser than water. Flash point 30 °F. Vapors heavier than air. Irritates the skin, eyes, and mucous membranes. Used to make pharmaceuticals and dyes.
Synonyms
Thiophene, polymers
IUPAC Name
thiophene
Canonical SMILES
C1=CSC=C1
InChI
InChI=1S/C4H4S/c1-2-4-5-3-1/h1-4H
InChI Key
YTPLMLYBLZKORZ-UHFFFAOYSA-N
Boiling Point
84.0°C at 760 MM HG
Melting Point
>350°C
Flash Point
Not applicable
Purity
95%
Density
1.066 g/cm3
Solubility
less than 1 mg/mL at 75 °F
Appearance
Powder
Application
Conducting polymer.
Refractive Index
1.52684 at 25 °C
LogP
log Kow = 1.81
Vapor Pressure
20 mmHg at 32 °F
Decomposition
WHEN HEATED TO DECOMPOSITION IT EMITS HIGHLY TOXIC FUMES OF SULFUR OXIDES.
Odor
SLIGHT AROMATIC ODOR RESEMBLING BENZENE

Computed Properties

XLogP3
1.8
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
0
Exact Mass
84.00337130 g/mol
Monoisotopic Mass
84.00337130 g/mol
Topological Polar Surface Area
28.2Ų
Heavy Atom Count
5
Formal Charge
0
Complexity
22.8
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
WO-2015138305-A1 Thermoplastic polymer compositions 2015-02-10
US-2017360067-A1 Alcoholic beverage substitutes 2014-12-09
US-2016075702-A1 New pyridopyrimidines derivatives compounds 2014-09-12
US-2016046653-A1 Silylation of aromatic heterocycles by earth abundant transition-metal-free catalysts 2014-08-06
US-2016020336-A1 Low band gap polymer compound, synthesis of thereof, and organic photovoltaic cell containing the same 2014-07-21
US-9206196-B1 Derivatives of benzoxazino quinoline, benzoxazino isoquinoline and processes for their preparation 2014-07-11
US-2016009744-A1 Heteroaryl compounds useful as inhibitors of sumo activating enzyme 2014-07-01
US-2015376271-A1 Dual pdgf/vegf antagonists 2014-06-28
WO-2015200905-A2 Dual pdgf/vegf antagonists 2014-06-28
WO-2015200425-A1 Topical dosage regimen 2014-06-27

Literatures

PMID Publication Date Title Journal
35977382 2022-09-08 GPCR Agonist-to-Antagonist Conversion: Enabling the Design of Nucleoside Functional Switches for the A2A Adenosine Receptor Journal of medicinal chemistry
35034442 2022-02-10 Discovery of Gut-Restricted Small-Molecule Inhibitors of Intestinal Sodium-Dependent Phosphate Transport Protein 2b (NaPi2b) for the Treatment of Hyperphosphatemia Journal of medicinal chemistry
34910929 2022-01-25 Inhibition of cytochrome P450 enzymes and uridine 5'-diphospho-glucuronosyltransferases by vicagrel in human liver microsomes: A prediction of potential drug-drug interactions Chemico-biological interactions
34351741 2021-08-26 Discovery, Synthesis, and Evaluation of Highly Selective Vascular Endothelial Growth Factor Receptor 3 (VEGFR3) Inhibitor for the Potential Treatment of Metastatic Triple-Negative Breast Cancer Journal of medicinal chemistry
33400020 2021-08-01 SEW2871 attenuates ANIT-induced hepatotoxicity by protecting liver barrier function via sphingosine 1-phosphate receptor-1-mediated AMPK signaling pathway Cell biology and toxicology
33567378 2021-03-15 Identification of novel potent HIV-1 inhibitors by exploiting the tolerant regions of the NNRTIs binding pocket European journal of medicinal chemistry
32265417 2021-02-01 Renal Function Improvement Following ANG-3777 Treatment in Patients at High Risk for Delayed Graft Function After Kidney Transplantation Transplantation
33075310 2020-12-01 A specific inhibitor of polo-like kinase 1, GSK461364A, suppresses proliferation of Raji Burkitt's lymphoma cells through mediating cell cycle arrest, DNA damage, and apoptosis Chemico-biological interactions
33143469 2020-12-01 Scaffold hopping and optimisation of 3',4'-dihydroxyphenyl- containing thienopyrimidinones: synthesis of quinazolinone derivatives as novel allosteric inhibitors of HIV-1 reverse transcriptase-associated ribonuclease H Journal of enzyme inhibition and medicinal chemistry
33210414 2020-12-01 Erdosteine salvages cardiac necrosis: Novel effect through modulation of MAPK and Nrf-2/HO-1 pathway Journal of biochemical and molecular toxicology
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Related Products

Online Inquiry
  • Verification code
USA
  • International:
  • US & Canada (Toll free):
  • Email:
  • Fax:
UK
  • Email:
Copyright © 2024 BOC Sciences. All rights reserved.
Inquiry Basket