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666-14-8

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666-14-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 666-14-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,6 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 666-14:
(5*6)+(4*6)+(3*6)+(2*1)+(1*4)=78
78 % 10 = 8
So 666-14-8 is a valid CAS Registry Number.

666-14-8Downstream Products

666-14-8Relevant articles and documents

Characterizing Cation Chemistry for Anion Exchange Membranes - A Product Study of Benzylimidazolium Salt Decompositions in the Base

Pellerite, Mark J.,Kaplun, Marina M.,Webb, Robert J.

, p. 15486 - 15497 (2019)

Imidazolium functionality has played a prominent role in research on anion exchange membranes for use in alkaline electrochemical devices. Base stability and degradation of these materials has been much studied, but in many instances, product pathways have not been thoroughly delineated. We report an NMR study of base-induced decomposition products from three benzylimidazolium salts bearing varying extents of methyl substitution on the imidazolium ring. The major products are consistent with a hydrolytic ring fragmentation pathway as the principal mode of decomposition. We observe several new products not previously reported in the literature on imidazolium salt degradation, including benzilic acid rearrangement products formally derived from intermediate 1,2-dicarbonyl compounds or their equivalents. However, the overall reactions are complex, the yields of observed products do not account for all consumed starting materials, and mechanistic ambiguities remain.

Room temperature, near-quantitative conversion of glucose into formic acid

Wang, Can,Chen, Xi,Qi, Man,Wu, Jianeng,G?zaydin, G?kalp,Yan, Ning,Zhong, Heng,Jin, Fangming

, p. 6089 - 6096 (2019/11/20)

Herein, a facile and efficient method was developed to selectively transform glucose into formic acid at room temperature. After parameter optimization, formic acid was obtained in an unprecedented 91.3% yield with a reaction time of 8 h in lithium hydroxide aqueous solution with hydrogen peroxide as the oxidant. The synergistic effects of the base and the oxidant promoted the glucose conversion at room temperature and enhanced the selectivity towards FA. Besides, the employed mild conditions have suppressed FA decomposition that often occurred under harsh conditions, which further improved the FA selectivity. A series of model compound tests were conducted to probe the possible intermediates based on which a plausible reaction pathway was proposed. In addition, the process is applicable to various carbohydrates such as cellobiose, starch, xylan, etc. This work opens up a simple, mild but effective method to produce FA from renewable biomass resources, which would remarkably alleviate the energy consumption, capital costs, handling risks, etc.

Synthesis of α-amino and α-hydroxy acids under volcanic conditions: implications for the origin of life

Huber, Claudia,Eisenreich, Wolfgang,W?chtersh?user, Günter

scheme or table, p. 1069 - 1071 (2010/04/05)

Facile synthesis of α-hydroxy and α-amino acids is observed at temperatures from 145 to 280 °C with catalytic Ni2+, with cyano ligands as source for C and N, and with CO as a reductant and as a source for C. Implications for the problem of the origin of life are discussed.

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