86738-35-4 Usage
Thiadiazole derivative
A compound based on the 1,3,4-thiadiazole ring structure This refers to the core structure of the molecule, which is a five-membered ring containing sulfur and nitrogen atoms.
Methylsulfonyl group
A CH3-SO2 functional group attached to the 2-position of the molecule This is a specific functional group that contributes to the compound's chemical properties and reactivity.
Phenyl group
A C6H5 functional group attached to the 5-position of the molecule This is another functional group that influences the compound's properties and reactivity.
Potential use as a pesticide
Ability to control or kill pests in agricultural settings This indicates one of the possible applications of the compound in controlling pests.
Antifungal agent
Capable of inhibiting the growth of fungi This suggests another potential application of the compound in preventing fungal growth.
Photoelectric material
A material used in organic electronic devices to convert light into electricity This highlights the compound's potential use in the field of organic electronics.
Investigated for anti-cancer properties
The compound has been studied for its potential to inhibit or prevent cancer growth This points to another area of research for the compound's potential applications.
Further research needed
More studies are required to fully understand the biological and practical applications of the compound This emphasizes that the current knowledge about the compound is limited, and additional research is necessary to explore its full potential.
Check Digit Verification of cas no
The CAS Registry Mumber 86738-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,3 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 86738-35:
(7*8)+(6*6)+(5*7)+(4*3)+(3*8)+(2*3)+(1*5)=174
174 % 10 = 4
So 86738-35-4 is a valid CAS Registry Number.
86738-35-4Relevant academic research and scientific papers
Tunable Heteroaromatic Sulfones Enhance in-Cell Cysteine Profiling
Motiwala, Hashim F.,Kuo, Yu-Hsuan,Stinger, Brittany L.,Palfey, Bruce A.,Martin, Brent R.
supporting information, p. 1801 - 1810 (2020/02/04)
Heteroaromatic sulfones react with cysteine via nucleophilic aromatic substitution, providing a mechanistically selective and irreversible scaffold for cysteine conjugation. Here we evaluate a library of heteroaromatic sulfides with different oxidation st
Thiadiazole sulfone compound as well as preparation method and application thereof
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Paragraph 0061; 0071; 0072, (2018/10/19)
The invention relates to the field of agricultural fungicides and discloses a thiadiazole sulfone compound as well as a preparation method and application thereof. The compound has a structure expressed by a formula (I) which is as shown in the descriptio
Synthesis and anticonvulsant activity of 5-aryl-1,3,4-thiadiazole derivatives
Foroumadi,Tabatabai,Gitinezhad,Zarrindast,Shafiee
, p. 31 - 33 (2007/10/03)
5-Aryl-1,3,4-thiadiazole derivatives were synthesized and tested for anticonvulsant activity using the pentylenetetrazole-induced lethal convulsion test. The results showed that 2-amino derivatives have anticonvulsant activity (LD50 > 500 mg kg-1) and this effect was not mediated through benzodiazepine receptors. The fluoro electron-withdrawing substituent on the phenyl ring did not potentiate the activity of the compounds.
Synthesis of 5-(Substituted Phenyl) 4-Acetyl-2-methylthio-Δ2-1,3,4-thiadiazolines and their Oxidation with Potassium Permanganate
Kubota, Seiju,Toyooka, Kouhei,Ikeda, Junichi,Yamamoto, Naoya,Shibuya, Masayuki
, p. 967 - 971 (2007/10/02)
The reaction of aldehyde methylthio(thiocarbonyl)hydrazones (2) with acetic anhydride or acetyl chloride gave 5-(substituted phenyl) 4-acetyl-2-methylthio-Δ2-1,3,4-thiadiazolines (3).Oxidation of compounds (3) with potassium permanganate in ace
