5-Ethyl-2-thiouracil, 98%

Name: 5-Ethyl-2-thiouracil, 98% | 34171-37-4
Brand: J&K Chemical
SKU: JK521370_1_G
Price: 132.0 USD
Availability: OutOfStock

Cat. No JK521370_1_G

Vendor: J&K Chemical

Product Information

Product Name

5-Ethyl-2-thiouracil, 98%

Brand Name

J&K

Product Number

521370

CAS

34171-37-4

Molecular Formula

C6H8N2OS

Molecular Weight

156.21

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

3002042

IUPAC Name

5-ethyl-2-sulfanylidene-1H-pyrimidin-4-one

InChI Key

JYBWJPAOAQCXAX-UHFFFAOYSA-N

SMILES

CCC1=CNC(=S)NC1=O

References

Table 4.1. Free enthalpies of adsorption of ions and organic molecules at metal electrodes

Publication Name: Landolt-Börnstein - Group IV Physical Chemistry

Publication Date: 2007

DOI: 10.1007/978-3-540-45316-1_20

Non‐nucleoside HIV Reverse Transcriptase Inhibitors, Part 6[1]: Synthesis and Anti‐HIV Activity of Novel 2‐[(Arylcarbonylmethyl)thio]‐6‐arylthio DABO Analogues

Publication Name: Archiv der Pharmazie

Publication Date: 2005-10

DOI: 10.1002/ardp.200400961

Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii

Publication Name: Biochemical Pharmacology

Publication Date: 1994-08-17

DOI: 10.1016/0006-2952(94)90057-4

4.11.2 Data

Publication Name: Physical Data II. Theoretical Investigations

Publication Date: 1990

DOI: 10.1007/10407393_58

The Mode of Action and Clinical Uses of the Thiouracil Group of Drugs

Publication Name: Ergebnisse der Inneren Medizin und Kinderheilkunde

Publication Date: 1949

DOI: 10.1007/978-3-642-94558-8_2

5-Ethyl-2-thiouracil, 98%

Product Information

General Information

References

Table 4.1. Free enthalpies of adsorption of ions and organic molecules at metal electrodes

Non‐nucleoside HIV Reverse Transcriptase Inhibitors, Part 6[1]: Synthesis and Anti‐HIV Activity of Novel 2‐[(Arylcarbonylmethyl)thio]‐6‐arylthio DABO Analogues

Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii

4.11.2 Data

The Mode of Action and Clinical Uses of the Thiouracil Group of Drugs