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9-hydroxybimol cyclic ester is a chemical compound derived from bimol, which is a synthetic analog of the natural product bimane. This cyclic ester is characterized by the presence of a hydroxyl group at the 9-position and a cyclic ester functional group. It is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique chemical properties and reactivity. The compound's structure allows for the formation of stable complexes and its ability to participate in various chemical reactions, making it a subject of interest for researchers exploring new synthetic pathways and applications.

797-29-5

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797-29-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 797-29-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,9 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 797-29:
(5*7)+(4*9)+(3*7)+(2*2)+(1*9)=105
105 % 10 = 5
So 797-29-5 is a valid CAS Registry Number.

797-29-5Downstream Products

797-29-5Relevant academic research and scientific papers

New and efficient method for the preparation of medium-sized lactones from the corresponding ω-hydroxycarboxylic acids

Mukaiyama, Teruaki,Izumi, Jun,Shiina, Isamu

, p. 187 - 188 (1997)

Medium-sized lactones are prepared in good yields on treating monomeric cyclic silyl siloxycarboxylates, prepared in situ from ω-hydroxycarboxylic acids and 1,2-bisdimethylsilylbenzene using RhCl(PPh3)3 catalyst, with an active catalyst of dimethylsilylbis(trifluoromethanesulfonate).

A facile synthesis of lipid stabilized gold nanoparticles: A step towards biodegradable biosensors

Abraham, Sinoj,Narine, Suresh S.

body text, p. 7027 - 7032 (2012/05/20)

A new class of polylactone was successfully synthesized and utilized for the encapsulation and stabilization of gold nanoparticles. Core/shell nanoparticle architecture, in which a layer of this polymer surrounds the nanoparticle core have been investigated both as a means to improve the stability and surface chemistry and as a way of accessing unique physical properties that are not possible from one nano-material alone. Given the fact that only few systems has so far been developed for the encapsulation of nanoparticles, our success in using a new biodegradable biopolymer with inbuilt functionality reveals the robustness of this work. The biodegradability of this polylactone was evaluated using scanning electron microscopy (SEM). The morphology and stability of these gold-polymer hybrids were evaluated by using the transmission electron microscopy (TEM) and UV-VIS spectroscopy.

Scandium trifluoromethanesulfonate as an extremely active Lewis acid catalyst in acylation of alcohols with acid anhydrides and mixed anhydrides

Ishihara, Kazuaki,Kubota, Manabu,Kurihara, Hideki,Yamamoto, Hisashi

, p. 4560 - 4567 (2007/10/03)

Scandium trifluoromethanesulfonate (triflate), which is commercially available, is a practical and useful Lewis acid catalyst for acylation of alcohols with acid anhydrides or the esterification of alcohols by carboxylic acids in the presence of p-nitrobenzoic anhydrides. The remarkably high catalytic activity of scandium triflate can be used for assisting the acylation by acid anhydrides of not only primary alcohols but also sterically-hindered secondary or tertiary alcohols. The method presented is especially effective for selective macrolactonization of ω-hydroxy carboxylic acids.

A New Synthetic Method of Macrocyclic Lactones from ω-Iodoalkylacrylates

Abe, Motoji,Hayashikoshi, Takaoki,Kurata, Takeo

, p. 1789 - 1792 (2007/10/02)

When the photostimulated cyclization reaction of ω-iodoalkylacrylates was performed in the presence of metal hydride complexes such as sodium cyanoborohydride (NaBH3CN), sodium borohydride (NaBH4) and potassium borohydride (KBH4), the corresponding macrocyclic lactones were produced.The use of NaBH3CN led to the highest yield of lactones.

Facile Synthesis of Lactones from Silyl ω-Siloxycarboxylates Using p-Trifluoromethylbenzoic Anhydride and a Catalytic Amount of Active Lewis Acid

Mukaiyama, Teruaki,Izumi, Jun,Miyashita, Mitsutomo,Shiina, Isamu

, p. 907 - 910 (2007/10/02)

The lactonization of silyl ω-siloxycarboxylates is successfully carried out under mild conditions in good to high yields by using p-trifluoromethylbenzoic anhydride and a catalytic amount of active acidic species generated in situ from TiCl4 and AgClO4.

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