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2-butyl-5-propylthiophene is an organic compound belonging to the class of thiophenes, which are heterocyclic aromatic compounds containing a sulfur atom. This specific compound has a molecular formula of C10H16S and consists of a thiophene ring with a butyl group attached to the 2nd carbon and a propyl group attached to the 5th carbon. It is characterized by its unique chemical structure, which contributes to its distinct properties and potential applications in various fields, such as organic synthesis, materials science, and pharmaceuticals. The compound's structure and properties make it a valuable building block for the development of new compounds with specific functions and characteristics.

4861-62-5

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4861-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4861-62-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,6 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4861-62:
(6*4)+(5*8)+(4*6)+(3*1)+(2*6)+(1*2)=105
105 % 10 = 5
So 4861-62-5 is a valid CAS Registry Number.

4861-62-5Upstream product

4861-62-5Downstream Products

4861-62-5Relevant academic research and scientific papers

Characterization of initial reaction intermediates in heated model systems of glucose, glutathione, and aliphatic aldehydes

Wang, Tianze,Zhen, Dawei,Tan, Jia,Xie, Jianchun,Cheng, Jie,Zhao, Jian

, (2020)

To understand the effect of lipid degradation on Maillard formation of meaty flavors, initial reaction intermediates in model systems of glucose–glutathione with hexanal, (E)-2-heptenal, or (E,E)-2,4-decadienal were identified by HPLC–MS and by NMR. Besides Amadori compounds, hemiacetals and thiazolidines via addition of sulfhydryl to carbonyl or to the conjugated olefinic bond were found. Concentrations of all intermediates increased with reaction time while degradation of the intermediates with a glutathione moiety helped formation of thiazolidines with cysteinylglycine. The unsaturated aldehydes (E)-2-heptenal and (E,E)-2,4-decadienal exhibited high reactivity against glucose for glutathione, yielding higher levels of intermediate compounds than from glucose. Heating prepared intermediates reversibly released the original aldehydes, which caused various compounds formed by retro-aldol, oxidation, etc. to react with H2S and NH3. Among them, formation pathways including 3-nonen-2-one, 2-hexanoylfuran, and six dialkylthiophenes (e.g., 2-ethyl-5-(1-methylbutyl)thiophene) were proposed for the first time.

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