Hétérocycles mixtes

<p>3-Chloro-1,2-benzisothiazole is a nucleophilic agent with a hydrogen bond donor. It has been shown to inhibit the replication of RNA in the presence of adenosine triphosphate (ATP) and to bind to amines. 3-Chloro-1,2-benzisothiazole is used as an inhibitor for non-nucleoside reverse transcriptase inhibitors. It has been shown to have high potency and strong inhibitory activity against HIV and other retroviruses. 3-Chloro-1,2-benzisothiazole also inhibits vibrational modes associated with enzymatic reactions.</p>

<p>Please enquire for more information about 5-Fluoro-dUMP sodium including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,5-Furandicarboxylic acid dimethyl ester is a structural analog of diacids. It has been synthesized by the reaction of 5-hydroxymethylfurfural with ethyl esters and phosphotungstic acid. The isolated yield was determined by gravimetric analysis. The structure of 2,5-furandicarboxylic acid dimethyl ester is shown in the following figure:</p>

<p>Interest in renewable based polymers has led to 2,5-furandicarboxylic acid being proposed as a green, sustainable alternative to the widely used petroleum-based terephthalic acid in the synthesis of polyesters. 2,5-Furandicarboxylic acid is produced from oxidation of 5-hydroxymethylfurfural (HMF) which is obtained from the dehydration of bio-based sugars such as fructose.</p>

<p>Please enquire for more information about 4-(Cyclopropylmethyl)-1-oxa-4,9-diazaspiro[5.5]undecan-3-one hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-Bromothiazole is an anticancer agent that can be prepared by coupling of 2-bromo-1,2-dithiolane and thiourea. This chemical has been found to be effective against a number of cancers in both animal and human studies. It is also used as a reagent in the industrial preparation of pesticides and dyes. 2-Bromothiazole is highly reactive with nucleophiles such as amines, alcohols, and phenols, which makes it a powerful catalyst for cross-coupling reactions. It can be used to make other organic compounds that have not been available from commercial sources due to its high reactivity. The compound's anti-inflammatory properties may be related to its ability to inhibit prostaglandin synthesis by inhibiting cyclooxygenase activity.</p>