Building Blocks

Versatile small molecule scaffold

Versatile small molecule scaffold

5-Bromo-2,3-dihydroxybenzaldehyde is a chemical compound that is used as a reaction component. It has been used in the synthesis of high quality research chemicals and speciality chemicals. This chemical has also been used as a useful scaffold for complex compounds and as a reagent for the synthesis of fine chemicals. 5-Bromo-2,3-dihydroxybenzaldehyde is soluble in water and can be stored at room temperature.

<p>2,6-Dimethylbenzoic acid is a colorless solid that has a molecular weight of 162.2 g/mol and an empirical formula of C7H8O2. It has a melting point of about 82 degrees Celsius and a boiling point of about 315 degrees Celsius. 2,6-Dimethylbenzoic acid is soluble in water at 100 degrees Celsius. It has been shown to act as a potent antagonist for the muscarinic acetylcholine receptors. This compound also has basic properties due to its hydrogen bonding interactions with proteins and other molecules. 2,6-Dimethylbenzoic acid has been shown to be efficient in supramolecular chemistry because it is electron deficient and contains thermodynamic functional groups such as carboxylic acids and alcohols.</p>

<p>1,6-Dimethoxynaphthalene is a chiral molecule that can be used as a chemical intermediate in the synthesis of pharmaceuticals. 1,6-Dimethoxynaphthalene has been shown to react with dopamine to form β-unsaturated ketones. This reaction is catalyzed by thionyl chloride. The product of this reaction can be reacted with a chloride, naphthalene or sulfinyl chloride to form five-membered diprotonated products. 1,6-Dimethoxynaphthalene also reacts with hydrosulfite to form sulfinyl functional groups, which can then be used as additives in other chemical reactions.</p>

<p>3,4-Dimethoxybenzylamine is an amine that is used in the synthesis of pharmaceuticals. It can be polymerized by heating with aqueous formaldehyde and hydrochloric acid to form a resin. 3,4-Dimethoxybenzylamine inhibits serotonin receptors, exhibiting inhibitory properties at concentrations of 10-5 M. 3,4-Dimethoxybenzylamine also has pharmacokinetic properties that are similar to vitamin B1. This compound has been shown to inhibit homogeneous catalysts and is used for coatings for ganglion cells.</p>

<p>Versatile small molecule scaffold</p>

<p>1-Amino-3-phenyl-2-propanone Hydrochloride is a versatile building block that can be used as a reagent and speciality chemical. It can also be used as an intermediate in the synthesis of other compounds and pharmaceuticals. 1-Amino-3-phenyl-2-propanone Hydrochloride is soluble in water, ethanol, ether, chloroform, benzene, and acetone. This product has a CAS No. 41173-00-6 and can be shipped to Canada.</p>

<p>2,3-Dihydroxy-3-phenylpropanoic acid is a monocarboxylic acid and a benzenes. It has been shown to have antimicrobial properties against bacteria such as Staphylococcus aureus, Proteus vulgaris, and Klebsiella pneumoniae. The monocarboxylic acid inhibits bacterial growth by binding to the beta subunit of the enzyme DNA gyrase, which is necessary for DNA replication. 2,3-Dihydroxy-3-phenylpropanoic acid also binds to the beta subunit of the enzyme RNA polymerase and prevents mRNA synthesis, thus inhibiting protein synthesis in bacteria. !-- --&gt; !-- --&gt; !-- --&gt; !-- --&gt; !-- --&gt; !-- --&gt; !-- --&gt;</p>

<p>4-(Hydroxymethyl)-2-methylthiazole (4HMT) is a scaffold that can be used as a building block for complex compounds. 4HMT has been shown to be an excellent reagent for the synthesis of heterocycles and other useful compounds. It is also useful in research, where it is often used as a reaction component. The high quality of 4HMT ensures that it is an excellent choice for use as a fine chemical or speciality chemical.</p>

<p>Versatile small molecule scaffold</p>

<p>3-(Bromomethyl)isoxazole is a linker that can be used in the synthesis of other biologically active compounds. It has been shown to have an inhibitory effect on agriculturally-important bacteria, including those producing lipopolysaccharides. 3-(Bromomethyl)isoxazole has also been shown to have antibacterial activity and hydrogen bond interactions. 3-(Bromomethyl)isoxazole forms a boronic ester which is an important functional group in organic chemistry. This linker can also be used as a coagulant in water purification systems.</p>

<p>Intermediate in organic synthesis</p>

Versatile small molecule scaffold

<p>6-Methylpyridine-2-carboxylic acid is a human metabolite that can be found in the serum matrix. It is part of a ternary complex formation with picolinic acid and fatty acid, which may result in an intramolecular hydrogen transfer from the methyl group to the oxygen atom of the carboxylic acid group. 6-Methylpyridine-2-carboxylic acid has been shown to react with hydroxyl groups to form n-oxides and redox potentials. These reactions are catalyzed by detergents.</p>

Methyl 4-acetylbenzoate is a synthetic compound that can be used for the synthesis of imatinib and other pharmaceuticals. It is an effective method for the synthesis of butyric acid with high enantiomeric purity. The cross-coupling reaction was first reported by Suzuki in 1979, which has been widely applied to organic synthesis because it is efficient and produces simple byproducts. This reaction has also been used in the synthesis of model compounds and natural products, as well as in environmental pollution studies.

2-Mercapto-5-benzimidazole sulfonic acid sodium salt dihydrate is a molecule that can be used in devices. It has been shown to reversibly change the morphology of a monolayer and to generate asymmetric structures. 2-Mercapto-5-benzimidazole sulfonic acid sodium salt dihydrate can be used to generate fluorescent emulsions, which are systems where the magnetic particles are suspended in an oil droplet and illuminated by light of an appropriate wavelength. The molecules that make up 2-Mercapto-5-benzimidazole sulfonic acid sodium salt dihydrate have been shown to function as acceptors for molecular orbitals, which are wave functions that describe electron distribution around the atomic nucleus. These properties make it a promising candidate for use in microscopy techniques, such as scanning tunneling microscopy (STM) or atomic force microscopy (AFM).

<p>3-Methoxyacetophenone is a bacterial metabolite that is produced by the metabolism of caproic acid. 3-Methoxyacetophenone has been shown to possess antibacterial activity against gram-positive bacteria and to inhibit protein synthesis in these bacteria. The compound class of 3-methoxyacetophenone includes methyl ketones, which are a type of organic compounds containing a carbonyl group (C=O). This compound can be found in bacterial strains such as Pseudomonas aeruginosa and Streptococcus pneumoniae. These bacteria produce 3-methoxyacetophenone during growth on l-tartaric acid or hydrogen tartrate as the sole carbon sources. The organism’s DNA sequences have been determined by deuterium isotope sequencing and l-tartaric acid as the sole carbon source.</p>

2-Methyl-1,3-propanediol is a glycol ether that is used in sample preparation for chemical analysis. It is an antimicrobial agent that has been shown to be active against bacteria such as Escherichia coli and Staphylococcus aureus. 2-Methyl-1,3-propanediol has also been shown to have the ability to inhibit the growth of epidermal cells. This chemical has been shown to be effective in treating skin lesions caused by dermatophytes, fungi and bacterial infections. 2-Methyl-1,3-propanediol inhibits the synthesis of glycol esters, fatty acids and epidermal growth factor through competition with hydroxyl groups on cell membranes. It also chelates metal ions such as Cu2+, Zn2+, Cd2+ and Pb2+.

<p>4-Methoxybenzenediazonium tetrafluoroborate (MBD) is a synthetic molecule that can be prepared by the reaction of sodium hydrogen with UV irradiation. MBD has been shown to have a pharmacokinetic profile similar to methyl cinnamate and is used in the treatment of hyperpigmentation, such as melasma and post-inflammatory hyperpigmentation. MBD interacts with the amino acid tyrosine at its 4-hydroxyl group, cleaving the C-O bond and forming an intramolecular hydrogen bond with the oxygen atom. This results in the formation of diazonium salt which reacts with tyrosinase and inhibits its activity.</p>