Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Bromo-6-iodo-4-methylaniline (BIOM) is an inorganic compound that has absorption spectroscopy properties. BIOM has a strong absorption band at 450 nm and a weak absorption band at 700 nm, which is indicative of the shift from the lower energy state to the higher energy state. This process, known as photochemical shift, is caused by the benzannulation of BIOM. The functional theory explains how this process occurs when BIOM absorbs light energy. The phenanthridinyl framework of BIOM ensures that it can be used as a ligand for transition metal complexes. This ligand also exhibits chiral properties. When BIOM absorbs light energy, it undergoes a red shift to its ground state because it is chiral and there are two possible pathways for the electron transfer. These pathways have different energies and produce different products.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-Benzylsulfamoylphenacetamide is a chemical compound with the molecular formula CHNO that contains a benzene ring, two-dimensional hydrogen bonding, an amide group, and a torsion angle. This chemical has been researched for its possible use as an antibiotic. 4-Benzylsulfamoylphenacetamide is a conformationally restricted molecule with coplanar bonds. It has been shown to have dihedral angles of 0° and 180°.</p>

<p>Versatile small molecule scaffold</p>

<p>Iodonicotinonitrile is a versatile and efficient regioselective coupling catalyst for the synthesis of substituted heteroaryl bromides. Iodonicotinonitrile converts potassium iodide to an iodonium salt with copper(I) chloride, which in turn reacts with aryl or heteroaryl bromides to give the desired products in high yields. The use of iodonicotinonitrile as a coupling agent provides advantages over other methods such as the addition of iodine to an aryl halide. The use of iodonicotinonitrile is advantageous because it can be used in both acidic and basic conditions and is also more efficient than other methods.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Bromo-5-iodobenzyl bromide is a monoclonal antibody that can be used in immunoassays. It recognizes an antigenic determinant on the surface of cells and binds to it specifically. The antibody has been used in immunosorbent assays for the detection of pesticides, which are usually present in small quantities. 2-Bromo-5-iodobenzyl bromide is a synthetic compound that is soluble in organic solvents and has reproducible yields.</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 3-[(2-methylpropyl)amino]propanoate is an activator of ion channels and a ligand for G protein-coupled receptors. It also has been shown to inhibit the activity of protein interactions, such as receptor-ligand binding. Methyl 3-[(2-methylpropyl)amino]propanoate can be used in research as a research tool, or in pharmacology for the treatment of diseases such as Alzheimer's disease and schizophrenia. Methyl 3-[(2-methylpropyl)amino]propanoate is soluble in DMSO, ethanol, and acetonitrile. It has a molecular weight of 214.27 g/mol and an empirical formula C8H18N2O3. The CAS Number is 289656-94-6.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Ethyl 3-amino-5-phenylfuran-2-carboxylate is a benzyl derivative that has been shown to have antimicrobial properties against many bacteria, including Gram-positive and Gram-negative bacteria. It is also active against fungi. Ethyl 3-amino-5-phenylfuran-2-carboxylate is synthesized by the reaction of aniline with carbon disulfide and sodium chloride in the presence of pyridine. The product then undergoes cyclization under acidic conditions to form ethyl 3-(aminocarbonyl)-5-(pyridinium)furan 2(3H)-carboxylate, which is then hydrolyzed to give ethyl 3-(aminocarbonyl)-5-(benzoyl)furan 2(3H)-carboxylate. This compound can be further modified to produce its antibacterial metabolite, benzoyl isothi</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold