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Uranium hexafluoride (UF6), also known as "Up2U," is a chemical compound consisting of uranium and fluorine. It is a colorless, odorless, and highly toxic gas at room temperature, with a molecular weight of 352.02 g/mol. UF6 is a key intermediate in the production of enriched uranium, which is used as fuel for nuclear reactors and in nuclear weapons. The compound is produced by reacting uranium tetrafluoride (UF4) with fluorine gas at high temperatures. Due to its volatility, UF6 is used in the gas diffusion process for uranium enrichment. It is also a significant contributor to the spread of nuclear weapons proliferation, as it can be converted back to metal uranium for use in nuclear devices. UF6 is subject to strict international controls and regulations to prevent its misuse.

26184-65-6

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26184-65-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26184-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,8 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26184-65:
(7*2)+(6*6)+(5*1)+(4*8)+(3*4)+(2*6)+(1*5)=116
116 % 10 = 6
So 26184-65-6 is a valid CAS Registry Number.

26184-65-6Downstream Products

26184-65-6Relevant academic research and scientific papers

Chemical synthesis and isolation of UDP-2-deoxy glucose and galactose

Miyagawa, Atsushi,Takeuchi, Shunya,Itoda, Shinji,Toyama, Sanami,Kurimoto, Kenta,Yamamura, Hatsuo,Ito, Yukishige

supporting information, p. 1790 - 1795 (2016/11/18)

2-Deoxy sugars are attractive compounds in synthetic chemistry with regard to reactivity and stereoselectivity. Moreover, their ability to inhibit enzymes and metabolism is significant in biology. In this study, uridine-5′-diphosphate (UDP)-2-deoxy glucose (11) and galactose (12) were synthesized chemically. These sugar donors for glycosyltransferases were obtained α-selectively via phosphorylation using thioglycosides, coupling reaction with uridine-5′-monophosphate (UMP)-morpholidate, and moderate deacetylation. Isolation was carried out by sequential silica-gel chromatography using two kinds of developing solvents in a refrigerator. The structures were elucidated from the NMR results. Investigation of stability showed that the synthesized UDP-2-deoxy sugars were hydrolyzed much faster in buffer (pH 4) than the natural UDP sugars.

A Simple synthesis of sugar nucleoside diphosphates by chemical coupling in water

Tanaka, Hidenori,Yoshimura, Yayoi,Jürgensen, Malene R.,Cuesta-Seijo, Jose A.,Hindsgaul, Ole

supporting information, p. 11531 - 11534 (2013/01/15)

Sugar nucleotides made easy: The new reagent ImIm , which is formed in-situ in water, is shown to activate nucleoside 5'-phosphates to their imidazolides, these can subsequently couple with sugar-1-phosphates; the whole procedure takes place in water. This truly simple method yields a crude product mixture that can be used directly as a source of donors for glycosyltransferase- mediated oligsaccharide synthesis. In the scheme, B stands for the nucleobases U, A, or G. Copyright

Optimization of UDP-N-acetylmuramic acid synthesis

Humljan, Jan,Starcevic,Car,Stefanic Anderluh,Kocjan,Jenko,Urleb

, p. 102 - 106 (2008/09/21)

UDP-N-acetylmuramic acid (UDP-MurNAc) is a substrate of MurC, an important enzyme in the intracellular pathway of bacterial peptidoglycan biosynthesis. Various approaches towards preparation of UDP-Mur/VAc have been published but these synthetic preparations were shown to include many problematic steps. An optimization study with the focus on muramyl phosphate and UMP-morpholidate coupling was performed, resulting in a synthetic procedure enabling robust and easily reproducible production on a multi-gram scale.

Multi gram synthesis of UDP-N-acetylmuramic acid

Dini,Drochon,Ferrari,Aszodi

, p. 143 - 145 (2007/10/03)

As part of an effort to discover novel antibacterial agents, a new and efficient synthesis was established in order to provide a large amount of UDP-N-acetylmuramic acid (UDP-MurNAc).

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