6-membered Rings

<p>Applications Monobenzyl Miglustat is a useful synthetic intermediate.<br></p>

<p>Applications 4-N-OCTYLOXYBENZOIC ACID (cas# 2493-84-7) is a useful research chemical.<br></p>

<p>Applications 3-Acetamidophenyl acetate<br></p>

<p>Applications Cyanomethyl Methyl(phenyl)carbamodithioate (cas# 76926-16-4) is a useful research chemical.<br></p>

<p>Applications Cyclohexylacetic acid<br></p>

<p>Applications Methyl 2-chloro-6-nitrobenzoate<br></p>

<p>Applications 3-Amino-2-hydroxybenzonitrile<br></p>

<p>Applications Wittig Reagent<br>References Yang, Z., et al.: Bioorg. Med. Chem., 17, 1071 (2009), Shearman, G., et al.: J. Mat. Chem., 19, 598 (2009),<br></p>

<p>Applications 2-benzylcyclopropane-1-carboxylic acid (cas# 103986-55-6) is a useful research chemical.<br></p>

<p>p-Toluenesulfonic acid monohydrate is a white, crystalline solid that is soluble in water. It is used as a catalyst for the synthesis of various organic compounds and pharmaceuticals. p-Toluenesulfonic acid monohydrate has been shown to have an effect on the thermal expansion of certain polymers and to be useful for preparation of medicinal preparations with high uptake. This compound can also be used as a carbon source for the production of various organic compounds.</p>

<p>3-Bromobenzenesulfonyl chloride is a molecule that can be used to inhibit the uptake of 3-bromobenzoate. The inhibition of uptake is due to the desymmetrization of the unsymmetrical, 3-bromobenzoate. This reaction leads to an increase in the concentration of 3-bromobenzoate. Inhibition studies have shown that 3-bromobenzenesulfonyl chloride has an inhibitory effect on cancer cells and apoptosis pathway. The structural studies have shown that this drug is synthetic and biphenyl can be synthesized from it. T-cell lymphomas have been shown to be inhibited by this drug and heart disease has also been inhibited.</p>

<p>1-Bromo-2-fluoro-3-nitrobenzene is a synthetic chemical that is used as an intermediate in the synthesis of various dyes. It can be obtained by the diazotization of acetyl nitrite and acetonitrile, followed by acetylation with acetic anhydride and hydrolysis with sodium hydroxide. The bromoaniline formed after this reaction is then converted to 1-bromo-2-fluoro-3-nitrobenzene by refluxing it with nitric acid. This chemical can also be synthesized from bromines and chloride in the presence of a diazo salt. It reacts with fluoride or halogens to produce fluorobenzene derivatives, which are used as intermediates for other organic compounds.</p>

<p>Please enquire for more information about alpha-Hydroxy-alpha-phenylbenzeneacetic acid (3-endo)-8-azabicyclo[3.2.1]oct-3-yl ester hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>