Building Blocks

<p>Cyclopentane-1,2-dicarboxylic acid is an organic compound with the molecular formula C5H8O4. The molecule consists of a cyclopentane ring and two carboxylic acid groups. Cyclopentane-1,2-dicarboxylic acid can be synthesized by an intramolecular cyclization reaction between a 1-bromocyclopentane and a chalcone. This reagent can also be used to synthesize other compounds such as phenoxyethanol, an enolate, and organozinc compounds.</p>

<p>(E)-3-Cyclohexylacrylic acid is an antibacterial agent that inhibits the growth of bacteria by binding to the 50S ribosomal subunit. It binds to bacterial 16S ribosomal RNA and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. (E)-3-Cyclohexylacrylic acid has been shown to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Clostridium perfringens, although is not active against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex. This compound also has anticancer activity, which may be due to its ability to inhibit topoisomerase II activity in cells.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>7H,8H-Imidazo[1,5-a]pyrazin-8-one is a potent and selective inhibitor of the bromodomain family. Bromodomains are protein domains found in many proteins that have been implicated in regulating gene expression, DNA repair, and protein degradation. Inhibiting this domain leads to decreased proliferation of tumor cells. 7H,8H-Imidazo[1,5-a]pyrazin-8-one has also shown potential as an anti-neurodegenerative agent by inhibiting the enzyme acetylcholinesterase. This compound is active against cancerous cell lines and is crystalline with a polymorphic form that can be used for medicine production.</p>

<p>8-Chloroimidazo[1,5-a]pyrazine is a potent insulin-like growth factor-I receptor (IGF-IR) inhibitor with potential therapeutic use for type II diabetes. It was found to inhibit IGF-I induced activation of the IR and downstream signaling pathways in a dose dependent manner. 8-Chloroimidazo[1,5-a]pyrazine inhibited IGF-I induced mitogenesis in human colon cancer cells and showed antiangiogenic activity in nude mice bearing xenografts of human colon cancer cells.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>2-Chlorocyclohex-1-ene-1-carboxylic acid is a synthetic compound that has been used as a reactant for the production of phthalic anhydride. The reaction mechanism begins with the formation of isocyanide, which reacts with benzoic acid to form an intermediate benzoyl isocyanide. This intermediate reacts with the acetic acid to produce 2-chlorocyclohexanecarboxylic acid, which in turn undergoes hydrolysis to give phthalic anhydride.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>5-Methyl-1H-indazol-4-amine is a tyrosine kinase inhibitor that has been shown to be potent in inhibiting the activity of various types of tyrosine kinases. It has good oral pharmacokinetics and is not metabolized by the liver. 5-Methyl-1H-indazol-4-amine binds to the ATP site on the enzyme and prevents phosphorylation, which inhibits cell proliferation and growth. This agent also inhibits DNA synthesis, protein synthesis, and phosphoinositide turnover in cells. 5-Methyl-1H-indazol-4-amine is an orally active inhibitor of tyrosine kinases with good oral pharmacokinetics and does not require metabolic activation by the liver. This agent may be used for the treatment of cancer or other diseases associated with uncontrolled cell growth.</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

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>4-(tert-Butyl)-2-chloropyridine is a ligand that has been used in the synthesis of a number of boronic acids and quinoline derivatives. It is also useful in cross-coupling reactions, which are nucleophilic substitution reactions involving two partners, such as an organometallic reagent and an organic halide or pseudohalide. The linker can be any group that connects the two partners together for these reactions. 4-(tert-Butyl)-2-chloropyridine is stable under acidic conditions, making it an excellent choice for coupling with amines to produce amides.</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>8-Bromooct-1-yne has a chiral carbon and is therefore optically active. It has a boiling point of about 44 degrees Celsius, and it is soluble in ether and chloroform but not in water. The compound is stable at temperatures up to 130 degrees Celsius, and it is soluble in benzene and acetone but not in acetone. 8-Bromooct-1-yne has an optical rotation of +10.5 degrees. The molecule can be monosubstituted with a hydrogen atom or halogen atom, which changes the optical properties of the molecule. 8-Bromooct-1-yne has dichroism when viewed under polarized light, which means that the molecule absorbs light differently when it is rotated by 90° compared to when it is rotated by 0°. The compound's fluorescence emission maxima are at 488 nm and 514 nm. 8-Bromooct-1-yne's con</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-(2-Phenylethoxy)acetic acid is an oleylethanolamide that has been shown to have antibacterial activity. It has been shown to activate lysosomal hydrolases and inhibit the growth of bacterial cells. 2-(2-Phenylethoxy)acetic acid also inhibits the synthesis of inflammatory molecules, such as leukotrienes, prostaglandins, and cytokines. This drug is a potent inhibitor of phospholipase A2 and can be used for the treatment of inflammatory diseases.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<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

<p>Versatile small molecule scaffold</p>

<p>5,8-Dibromoquinoline is a synthetic trisubstituted quinoline derivative that has been shown to form frameworks with nitrogen atoms. It has been synthesized from 2-hydroxyphenylacetic acid, which upon dehydration gives the corresponding n-oxide. 5,8-Dibromoquinoline forms an acidic solution in water and an alkaline solution in ethanol. 5,8-Dibromoquinoline can be hydrolysed by both acidic and alkaline conditions to produce 2,4-dichlorobenzene and 2-bromophenol. The reaction is stereoselective with the formation of only one product.</p>

<p>Please enquire for more information about Trimethyl(trifluoromethyl)silane including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>Imazapyr is a herbicide that inhibits the activity of acetolactate synthase, an enzyme essential for plant growth. Imazapyr binds to the active site of acetolactate synthase and forms a stable complex with the enzyme, thereby inhibiting its activity. Imazapyr has been shown to have a low toxicity in mammals and is not absorbed through skin or lungs. This herbicide is also toxic to plants and fish, as it inhibits their growth by disrupting photosynthesis. Imazapyr does not bind to DNA, thus it does not induce mutations in bacterial chromosomes.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>1H-Indazol-4-ol is a synthetic chemical with the molecular formula CHNO. It is the chloride, nitro, diammonium, enamine, divalent, methyl ester, acrylonitrile, polyethylene terephthalate and anion form of 1H-indazole. 1H-Indazol-4-ol is used in the synthesis of aminonaphthalenes and triazoles. The polymerization reaction for the production of cellulose acetate is also catalyzed by 1H-indazole. This chemical has been shown to have anion properties in solvents such as water and alcohols.</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>N-(Methylcarbamoyl)acetamido N-methylcarbamate (NMCA) is a novel anti-cancer compound that selectively binds to the CB2 receptor. NMCA has been shown to inhibit the growth of cancer cells in vitro and in vivo, as well as reduce the size of bowel tumors. It also has a beneficial effect on cardiac function. The mechanism of action is not completely understood, but it may be due to binding to the CB2 receptor and blocking the activation of other receptors such as TNF-α. NMCA can be formulated into biocompatible polymers that are suitable for drug delivery. Furthermore, this compound can be used for treating inflammatory bowel disease and renal cell cancer.</p>

<p>2-Methylcyclopropanecarboxamide is a compound that has been shown to have anticoagulant properties. It binds to the active site of coagulation factor Xa and inhibits its activity, thereby preventing blood clots from forming. 2-Methylcyclopropanecarboxamide has also been shown to be an immunosuppressant, demonstrating a decrease in antibody response and reduced intestinal inflammation in mice. This drug has potential use as an anti-inflammatory agent or for the treatment of autoimmune diseases.</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>3-bromo-1-methyl-1H-indole is a chemical compound with the molecular formula C8H7BrN. It can be prepared by reacting 1,3-dimethylindole with bromine in the presence of potassium carbonate and palladium chloride. 3-Bromo-1-methyl-1H-indole has been used to synthesize tetramers of 1,3,5,7,9,11,13,15-(2)naphthacenecarboxylic acid. This compound has also been used as a lithiation reagent for substituted anilines and benzamides. The substituents on the indole ring allow for cyclic reactivity and functional groups that are reactive towards hydrolysis or lithiation. 3bromo 1methyl 1H indole is an example of a heterocyclic compound because it contains two rings. The first ring consists of five carbons</p>

<p>2-(4-Chloro-3-nitrobenzenesulfonamido)acetic acid is a fluorinated monosaccharide that is synthesized from 2,4-dichloro-3 nitrobenzenesulfonic acid and acetic anhydride. It has been used in the synthesis of oligosaccharides, complex carbohydrates, and glycosylations. This chemical has been shown to be effective as a methylating agent for sugars and carbohydrates. It is also used in click chemistry modifications and has CAS number 81473-65-6.</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>[(Pent-4-en-1-yloxy)methyl]benzene is an ester that is used in the synthesis of other compounds. It is produced by the catalytic cleavage of sulfoxides and interacts with a variety of ligands. [(Pent-4-en-1-yloxy)methyl]benzene can be used as a precursor to allylic esters, which are important in organic synthesis because they are often more reactive than their parent olefin. It has been shown to undergo allylic oxidation and allylic esters, which are important reactions in organic chemistry. Allylic oxidation involves the addition of oxygen to an unsaturated carbon atom, while allylic esters involve the addition of an alcohol to an unsaturated carbon atom. This functionalization process is useful for making molecules that contain two different types of functional groups.</p>

<p>Versatile small molecule scaffold</p>

<p>Methyl 4-amino-5-methylthiophene-3-carboxylate (AMTC) is a synthetic inhibitor of the enzyme acetyl-coa carboxylase. AMTC is used as a research tool to study the role of acetyl-coa carboxylase in plants and animals. In Arabidopsis, AMTC inhibits the synthesis of fatty acids, leading to reduced seed oil content. It also inhibits transcarboxylase in wheat, which causes an accumulation of acetate. AMTC is synthesized by reacting methyl 4-nitrobenzoate with thieno[2,3,-c]pyrazole in the presence of palladium(II) chloride and potassium carbonate. The product undergoes hydrogenation to give AMTC.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Quinazolone is an organic compound that can be classified as a hydrocarbon, aliphatic hydrocarbon, or a radical. It has been used in the production of benzyl, growth regulators and biocides. Quinazolone is also used for plant growth and is effective against some fungi such as Penicillium notatum.</p>

<p>Versatile small molecule scaffold</p>

<p>Cycloheptyl isothiocyanate is a 1-4c alkyl, azaheterocycle, isothiocyanate that has been shown to be stereoselective. It binds to the sulfur atom of thiols and sulfonylureas, preventing the formation of the reactive intermediate that leads to their hydrolysis. This property can be used for the synthesis of ensembles and aralkyls. Cycloheptyl isothiocyanate also binds to alkenyl groups, which may be useful in synthesizing cycloalkyls or haloalkyls.</p>

<p>3-Amino-4-iodo-1H-pyrazole is a heterocyclic organic compound consisting of an imidazole ring with a pyrazole ring fused at the 2 and 5 positions. It is an analog of pyridazine. The crystal structure of 3-amino-4-iodo-1H-pyrazole has been determined to be orthorhombic, with space group Pnam2. The compound has a number of reactions, including nucleophilic addition, hydroxylation, and nitration. This heterocyclic compound is reactive and can serve as a monofunctional reagent in multiple reactions. 3-Amino-4-iodo-1H-pyrazole is used in the synthesis of other related compounds like 6-(3′,5′ -diamino)imidazo[2,1]benzothiazoles.</p>