Building Blocks

Versatile small molecule scaffold

Silver trifluoromethanesulfonate (AgOTf) is a precursor in the synthesis of alpha-bromo-m-tolunitrile. It is a colorless, odorless solid that can be prepared by the reaction of silver ions with bromine and toluene in an aqueous medium. The profile of AgOTf has been studied by titration method and it has been shown to have an oxadiazole group. This molecule also has anticancer activity against cancer cells. Alpha-Bromo-m-tolunitrile is currently being investigated for its potential use as a drug candidate for the treatment of cancer, with particular interest in the inhibition of angiogenesis and metastasis.

Please enquire for more information about tert-Butyl azetidine-3-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Benzamide adenine dinucleotide triethylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

8-Bromoisoquinoline is a bifunctional alkylating agent that is used to synthesize esters and amides. It is commonly used for the synthesis of amino acids, peptides, and other biologically active molecules. 8-Bromoisoquinoline has been shown to have a synergistic effect with hydroxyalkyl carbamates, which may be due to its ability to form an ionic bond with the carboxylic acid in these compounds. This chemical can also react with nitro groups and serve as a chlorinating agent, as well as react with anions such as phosphate and acetate. 8-Bromoisoquinoline can be synthesized by reacting ethyl bromoacetate with tetrahydroisoquinolinium chloride in hydrochloric acid or isopropyl alcohol.

2-Bromo-1,3,5-triisopropylbenzene is an ethylene acetal that is prepared by the catalyzed reaction of aryl chlorides and anhydrous zinc bromide in the presence of triethylamine. The selectivities of this method are high because it can produce mainly a single isomer. The stereoselectivity is also high because the reaction proceeds with the formation of only one stereoisomer. The mechanism for this reaction involves a nucleophilic substitution of the halogenated aryl chloride with the trialkylborane, which generates two different products. This product has been used in the synthesis of biphenyls and nitro compounds.

4-Cyanobenzoic acid (4CB) is a benzene derivative that inhibits the activity of tyrosinase, an enzyme involved in the production of melanin. It is synthesized by reacting 2,4-dichlorobenzoic acid with sodium hydroxide and acetone. 4CB has been shown to have a potent inhibitory effect on the enzyme, with an isolated yield of up to 83%. The compound also shows strong hydrogen bonding interactions with water molecules and coordinates in a geometry where one of its oxygen atoms is double bonded to two nitrogen atoms. This structural analysis suggests that 4 CB may bind to tyrosinase through adsorption mechanism.

4-Chloropyrimidine HCl is a covalent molecule that contains 4-chloropyridine and hydrogen chloride. It exists as two tautomers, the enol form and the keto form. The protonation of the proton on nitrogen will determine which tautomer it will exist in. When there is no proton present, the molecule will exist in its enol form. Resonance is also an important factor with this molecule because it can have a variety of resonance forms. Resonance spectrometry has been used to identify 4-chloropyrimidine HCl because it produces a specific resonance pattern when exposed to magnetic fields. 4-Chloropyridinium trifluoroacetate is another name for this compound that is formed when the chlorine atom bonds with trifluoroacetic acid. This chemical does not have any interactions with azide but can react with tetrazole to produce a stable compound, which can be easily

Clonidine hydrochloride is a drug used in the treatment of hypertension and other cardiac diseases. It belongs to the class of drugs called centrally acting alpha-2 adrenergic agonists. Clonidine hydrochloride is also used for its antihypertensive effects in patients with neurogenic orthostatic hypotension, diabetic neuropathy, and glomerular filtration rate. The long-term efficacy and safety profile of clonidine hydrochloride has been established in clinical trials that have shown it to be effective in reducing symptoms of chronic pain and opioid withdrawal, as well as improving quality of life. Clonidine hydrochloride may be administered orally or transdermally. Clonidine binds to both alpha-1 and alpha-2 adrenergic receptors, which are responsible for vasoconstriction, inhibition of renin secretion from the kidneys, decreased sympathetic nerve activity, and increased parasympathetic nerve activity. This drug also has a protective effect on bone cancer cells

Inhibitor of SIRT1 deacetylase

4-Chloro-2-nitrotoluene is a chemical compound that is a nitro derivative of toluene. It is a white crystalline solid with the formula CHClNO. 4-Chloro-2-nitrotoluene has been shown to have constant boiling point, vibrational frequency and zirconium content at constant pressure. The thermodynamic properties of this compound are also constant, with values for free energy and entropy being -28.5 and 115.5 respectively. The molecule can be described by the functional theory, which states that it contains one nitro group and one monocarboxylic acid group in its molecular structure. 4-Chloro-2-nitrotoluene can be optimised using computational methods such as databases or molecular modeling software where it can be introduced into other molecules to form new compounds.BR>BR> 4-Chloro-2-nitrotoluene (CH

Cyclopropanesulfonyl chloride (CPSC) is a bicyclic heterocycle that has been shown to have potent inhibitory activity against the human pathogens hepatitis B virus, dengue virus, and influenza A virus. CPSC inhibits the NS3 protease of these viruses by forming hydrogen bonding interactions with the nucleophilic nitrogen atom of the enzyme and also by competing with a chloride ion for binding to the chlorine atom on the enzyme. It also inhibits HIV-1 infection in cell culture experiments. CPSC has been found to be effective in preventing inflammation caused by cytokines, such as interleukin-1β, tumor necrosis factor-α, and prostaglandin E2. The inhibition of inflammatory cytokines may be due to its ability to bind glucocorticoid receptors.

Cyanomethylenetributylphosphorane (CMTP) is an agent used for the diagnosis of body formation. It is a chemical compound that can be used to produce images of tissue and organs by detecting apoptosis, or programmed cell death. CMTP binds to the glucose-dependent insulinotropic polypeptide receptor (GIPR), stimulating the release of insulin in the pancreas. CMTP also has therapeutic potential for metabolic disorders, as it has been shown to reduce triglycerides and increase HDL cholesterol levels in human serum. CMTP is synthesized from trifluoroacetic acid, which is then reacted with a cyclic peptide containing an amino acid derivative and 1-methyl-2-pyrrolidinone. This reaction produces a molecule with one free amino group at one end and two free carboxylic acid groups at the other end. The molecule can be reacted with epidermal growth factor (EGF) or insulin to

Please enquire for more information about Docosane including the price, delivery time and more detailed product information at the technical inquiry form on this page

Versatile small molecule scaffold

Versatile small molecule scaffold