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6-hydroxy-1-methyl-2-(methylsulfanyl)pyrimidin-4(1H)-one is a heterocyclic organic compound characterized by a pyrimidin-4(1H)-one core structure, which features a six-membered aromatic ring with two nitrogen atoms at positions 1 and 3. 6-hydroxy-1-methyl-2-(methylsulfanyl)pyrimidin-4(1H)-one is further modified by the presence of a hydroxyl group at the 6-position, a methyl group at the 1-position, and a methylsulfanyl (methylthio) group at the 2-position. The combination of these functional groups gives the molecule unique chemical properties and potential applications in various fields, such as pharmaceuticals or agrochemicals, where it may serve as a building block for more complex molecules or as a precursor in chemical synthesis.

6945-56-8

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6945-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6945-56-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6945-56:
(6*6)+(5*9)+(4*4)+(3*5)+(2*5)+(1*6)=128
128 % 10 = 8
So 6945-56-8 is a valid CAS Registry Number.

6945-56-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-hydroxy-1-methyl-2-methylsulfanylpyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 6-hydroxy-1-methyl-2-(methylsulfanyl)pyrimidin-4(1h)-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6945-56-8 SDS

6945-56-8Relevant academic research and scientific papers

APOPTOSIS INHIBITORS

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Paragraph 0531, (2018/02/27)

The invention provides compounds that are inhibitors or covalent modifiers of succinate dehydrogenase subunit B (SDHB) and/or inhibitors of apoptosis, and pharmaceutically acceptable salts, hydrides and stereoisomers thereof. The compounds are employed in pharmaceutical compositions, and methods of making and use, including treating a person in need thereof with an effective amount of the compound or composition.

Convenient synthesis of toxoflavin that targets β-catenin/TCF4 signaling activities

Mao, Yongjun,Tian, Wang,Huang, Ziwei,An, Jing

, p. 594 - 597 (2014/06/10)

A rapid and improved route for synthesis of toxoflavin, an antibiotic and antitumor agent, is described. The method uses easily obtained materials and simple and practical reactions, including chlorination, condensation, and diazotization to produce toxoflavin in five steps with 14.2% yield and 98.6% purity (HPLC). This synthetic toxoflavin effectively inhibited β-catenin/Tcf4 driven TOP-luciferase activity with an IC50 of less than 0.5 μM and induced colon cancer cell death in a dose-dependent manner with an IC50 of 0.29 μM.

Pesticidally active O-alkyl-O-[1,6-Dihydro-1-substituted-6-oxo-pyrimid in-4-yl]-(thiono) (thiol) phosphoric (phosphonic) acid esters and ester-amides

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, (2008/06/13)

O-alkyl-O-[1,6-dihydro-1-substituted-6-oxo-pyrimidin-4-yl]-(thiono) (thiol) phosphoric (phosphonic) acid esters and ester-amides of the formula STR1 in which R represents alkyl, R1 represents alkyl, alkoxy, alkylthio, monoalkylamino or phenyl, R2 represents hydrogen, alkyl, alkoxy, alkylthio or dialkylamino, R3 represents alkyl or alkenyl, R4 represents hydrogen, alkyl or halogen, and X represents oxygen or sulphur, Which possess insecticidal, acaricidal and nematicidal properties.

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