Composés aliphatiques et dérivés

S18750 - 2-Trimethylsiloxy-1,3-butadiene

M03998 - Salubrinal

Please enquire for more information about 3-(4-Methoxyphenyl)adamantane-1-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Bromo-1-butene is a colorless liquid with a boiling point of 102°C. It is soluble in ethanol, acetone, and chloroform. 4-Bromo-1-butene undergoes an acid-catalyzed phase transition to the solid form at temperatures below its melting point. 4-Bromobutene can be synthesized by reacting ethyl bromide with 1-butene in the presence of a catalyst such as copper or silver oxide. The kinetic energy of the reaction is determined by measuring the rate of evolution of hydrogen bromide gas from the reaction mixture. The β-unsaturated ketone reacts with dimethyl fumarate in the presence of sodium hydroxide to produce 4-bromobutene and 2,2'-difluoroethanol. This product has been shown to have IR spectra similar to those for other products containing a hydroxyl group such as phenol and

2-Heptanethiol is an enantiopure chiral compound that is used in food chemistry as a kinetic reagent for the determination of aldehydes. It has been shown to be effective in the analysis of capsicum annuum and its microflora. 2-Heptanethiol has also been used for the preparation of thioacetic acid and hplc analysis. This compound is magnetic and can be used for chromatographic separations. The reaction products with 2-heptanethiol are magnetic, which makes it possible to study their reactions by magnetic resonance spectroscopy.

BR1119 - Allyl bromide

Extender in polyurethane synthesis

1-Adamantanecarboxylic acid methyl ester is a specialized chemical compound, classified as an ester derivative from the adamantane structure. It is sourced through the esterification of 1-adamantanecarboxylic acid, often involving methanol as a reagent under catalyzed conditions. The compound's mode of action is primarily as an intermediate in organic synthesis, where it enables the introduction of adamantyl groups into target molecules, influencing molecular structure with its bulky, rigid framework.This ester derivative finds extensive application in the realm of synthetic organic chemistry. It serves as a crucial intermediate in the development of complex organic materials and pharmaceuticals, where the adamantane moiety is required to confer specific steric and electronic properties. The incorporation of adamantane from 1-adamantanecarboxylic acid methyl ester can enhance the thermal stability, lipophilicity, and rigidity of the resultant compounds, making it invaluable for researchers focused on material sciences and drug development. Its versatile reactivity and robust structure make it a sought-after compound for advancing chemical research and innovation.