Benzenes

<p>M04150 - p-Nitrophenyl N-acetyl-beta-D-cellobiopyranoside</p>

<p>3-Hydroxy-4-methylbenzaldehyde is a chemical that is synthesized from 3-hydroxy-4-methylphenol and dimethylformamide. It has been shown to interact with aluminium, which may be due to its ability to form a 1:1 complex with the metal. 3-Hydroxy-4-methylbenzaldehyde also exhibits electrochemical methods and isomers with other aldehydes. This chemical can be used in gas chromatography/mass spectrometry (GCMS) as an internal standard for fatty acid analysis.</p>

<p>4-(Trifluoromethylthio)benzaldehyde is a magnetic, stereogenic, mononuclear compound with a thermodynamic stability that has been improved by advances in the field of thermodynamics. The compound can also be synthesized using an asymmetric synthesis and is tetrasubstituted with antiferromagnetic coupling. 4-(Trifluoromethylthio)benzaldehyde has many functions, including being able to control the oxidation-reduction potentials of lanthanide ions and ferromagnetic materials. It also has a calorimetry effect on the adsorption of water vapor onto hydrophobic surfaces.</p>

<p>3,4-Dihydroxybenzylamine hydrobromide is a chemical that reacts with hydrogen peroxide to produce light. It is used as a nutrient for the chemiluminescent reaction in a nutrient solution to detect dopamine, chlorogenic acids, and trifluoroacetic acid. 3,4-Dihydroxybenzylamine hydrobromide can also be used as an analytical method for the measurement of cortisol concentration in plasma and saliva samples. This chemical analogically reacts with monoamine neurotransmitters such as dopamine and gamma-aminobutyric acid (GABA) to form fluorescent probes. 3,4-Dihydroxybenzylamine hydrobromide is not toxic or mutagenic and has been shown to be safe for use in humans.</p>

<p>3,5-Dichloro-2-methoxybenzoic acid (3,5-DMB) is a diphenyl ether with a pharmacokinetic half-life of about 3 hours. It has two isomers: the cis and trans forms. The cis isomer is more active than the trans form. The cis isomer has been shown to be effective in treatments for amine oxidase inhibitors and short-chain fatty acids. It also has growth regulator properties that are used in treatments for psoriasis and acne. 3,5-DMB inhibits bacterial growth by binding to the enzyme dioxygenase, which catalyzes the conversion of 4-hydroxybenzoic acid into 4-hydroxyphenylpyruvic acid; this prevents the production of catecholamines and subsequent cell proliferation. This drug binds to apical membranes in the intestine by attaching to sulfhydryl groups on proteins involved in transport processes, preventing uptake</p>

<p>2,4,6-Trimethylbenzoic acid is a molecule that belongs to the class of carboxylates. It has been shown to exhibit anticarcinogenic properties in patients with cervical cancer. 2,4,6-Trimethylbenzoic acid inhibits the growth of cervical cancer cells by blocking the activation of ferrocenecarboxylic acid (FCCA). This compound also blocks the activity of hydrogen bond and nitrogen atoms that are essential for cell division and development. 2,4,6-Trimethylbenzoic acid is used as an intermediate in the production of ferrocene derivatives. It can be used for acylation reactions with aromatic or aliphatic amines under acidic conditions.</p>

<p>3,5-Dihydroxy-4-methylbenzoic acid methyl ester is a fine chemical that is used as a versatile building block in the synthesis of pharmaceuticals, agrochemicals and other chemicals. It can be used as an intermediate in the synthesis of organic compounds and research chemicals. This compound is also used as a reaction component in organic syntheses and is often found in speciality chemicals. 3,5-Dihydroxy-4-methylbenzoic acid methyl ester is soluble in most solvents and has high purity. It is a complex compound that can be used as a useful building block or reagent for many different reactions.</p>

<p>Please enquire for more information about 2-(Diphenylamino)benzoic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Hydroxy-2-iodobenzaldehyde is a heterocyclic compound that is synthesized from an acetoacetic ester. It is a photochemical precursor to many organic compounds, such as phenanthrene. The synthesis of 3-hydroxy-2-iodobenzaldehyde can be achieved by reacting acetoacetic acid with iodine and sodium nitrite in the presence of a base. This reaction yields 2-iodobenzoic acid in addition to the desired product. 3-Hydroxy-2-iodobenzaldehyde has been studied for its use in the preparation of natural products and research advances.</p>

<p>4-Cyanobenzaldehyde is an acid that inhibits tyrosinase, an enzyme involved in the production of melanin. It has been shown to have a strong inhibitory effect on the activity of this enzyme in a variety of biological studies. 4-Cyanobenzaldehyde is chemically stable and does not react with hydrochloric acid or water at room temperature, making it suitable for use in experiments involving these substances. This chemical also has antiinflammatory properties and can be used as a substitute for phenols in some chemical reactions. 4-Cyanobenzaldehyde is soluble in methanol and reacts with diphenolase, an enzyme involved in the synthesis of lignin, to produce benzophenone and benzoic acid. This reaction may be important for the formation of lignin during wood decomposition.</p>