Building Blocks

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-Benzylcyclobutanone is a chiral, cyclic, sulfoxide that is synthesized via the asymmetric synthesis of 3-benzoylcyclobutanone and benzaldehyde. It can be used in the preparation of oxazolidinones, which are synthetic drugs with anti-inflammatory, analgesic and antipyretic properties. The optical purity of 3-benzylcyclobutanone has been shown to be greater than 99% by chiral GC analysis. This compound has also been synthesized using a preparative yield of 92%.</p>

<p>3-Ethylmorpholine hydrochloride is a tryptic that is used to detect fingerprints, viruses, and tissue. It reacts with amines to form a product that can be detected by chromatography. 3-Ethylmorpholine hydrochloride has been shown to react with the transition state of the enzyme trypsin and inhibit its activity. 3-Ethylmorpholine hydrochloride is also reactive towards benzene, which may be due to its ability to form sulphone or primary amine intermediates. This would allow 3-Ethylmorpholine hydrochloride to undergo reactions with other solvents in the environment, such as cellular proteins in host cells.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>3-(4-Methoxy-phenyl)-1H-indazole is a kinase inhibitor that inhibits the activity of terminal kinases. It has been shown to inhibit the activity of indazole derivatives and may be useful in treating diseases associated with these kinases, such as cancer. 3-(4-Methoxy-phenyl)-1H-indazole is a potent inhibitor of human caspase 9, which plays an important role in apoptosis by activating downstream proteases. It also inhibits the activation of protein kinase B, which is involved in cellular signaling pathways and cell cycle regulation.</p>

<p>2-Amino-1-(4-methoxyphenyl)ethanol is a lactam that is minimally reactive with biological systems. It has been shown to inhibit the binding of the linker molecule to calcitriol, which is a vital component of vitamin D synthesis. This compound can also be used in intra-articular injections for the treatment of arthritis and other inflammatory disorders. 2-Amino-1-(4-methoxyphenyl)ethanol has been synthesized from an endogenous amino acid precursor and conjugated with a fluorophore, enabling it to be tracked in vivo by fluorescence imaging. It has been demonstrated that 2-Amino-1-(4-methoxyphenyl)ethanol can be used as a traceless bioactive molecule in molecular modelling and simulations.</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>1-Isocyanato-3-(propan-2-yl)benzene is a chiral molecule that has been synthesized and characterized by spectroscopic techniques. It is a colorless liquid with a boiling point of 137°C and an elution time of 12 minutes in high-performance liquid chromatography (HPLC). The compound exhibits strong absorption bands at 220 nm, 276 nm, and 332 nm in the UV region. NMR spectroscopy shows that the compound has a phenyl group nature. The compound also displays dichroism characteristics with correlation to the amylose content.</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-Chloropyridine-2,6-dicarbonitrile (4CP) is a ruthenium(II) complex that has been used in solar cells because of its high efficiency. It has been shown to be an efficient acceptor for singlet excitation and has a long fluorescence lifetime. 4CP is also able to generate electron transfer from the excited state to the ground state, leading to increased efficiencies in solar cells. 4CP is a pyridine compound that can be synthesized by reacting benzene with pyridine in the presence of activated charcoal at 400 °C.</p>

<p>3-(1-Ethoxyvinyl)-4-methylpyridine is a dipolar molecule that has been synthesised. It has been shown to undergo hydrolysis and decarboxylative reactions. The systematic study of the pyridine derivatives revealed the formation of isomeric 3-ethoxycarbonyl-4-methylpyridines, which were synthesized by reacting phenylhydrazine with esters of pyridine or pyrazole. The carbon atom in the pyridine ring can be either an ester or a hydroxyl group, which gives rise to different structural isomers. These compounds have been shown to have antihistaminic effects, which may be due to their ability to inhibit histamine release from mast cells.</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>

<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>

<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>

<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>1,4-Dichloro-2-butyne is a colorless liquid with a sweet odor. It is used as an intermediate in organic synthesis. 1,4-Dichloro-2-butyne can be prepared by the reaction of ethylene diamine and benzyl chloride in the presence of xylenes to form the corresponding ethyl diazoacetate. The ethyl diazoacetate is then reacted with chlorosulfonic acid to produce 1,4-dichlorobutane. This compound can be converted into other compounds such as amides, ethers, and esters using ethyl diazoacetate.</p>

<p>2,3-Diaminobenzoic acid is a benzimidazole derivative that is used in the treatment of microbial infections. It has been shown to inhibit the growth of bacteria by binding to their ribosomes and inhibiting protein synthesis. The reaction solution of 2,3-diaminobenzoic acid has fluorescence properties that can be used to detect contaminating substances. The conjugates formed with p-hydroxyphenylacetic acid are more soluble than those formed with hydroxybenzoic acid. 2,3-Diaminobenzoic acid is not very toxic and does not cause any detectable changes in enzyme activities or other biochemical parameters in short term exposure. It can be easily decomposed by sodium chloride into chlorine gas and hydrochloric acid, which are both highly reactive with water.</p>

<p>Please enquire for more information about 4,4'-Dithio-2,2'-bipyridine including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

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