Building Blocks

Versatile small molecule scaffold

<p>7-Benzyl-2,6-dichloro-7H-purine is a reagent that is used in the synthesis of adenine and other purines. It can be synthesized by coupling 3-methylxanthine with aminoacids and organometallic reagents. This chemical can also be used to selectively synthesize 6-benzyladenine, which is an important precursor to pharmaceuticals. The 7-benzyl group on this chemical has been shown to act as a positional group in the catalytic hydrogenation of amines. This selective hydrogenation process has been found to be regioselective for cycloalkyl amines.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

2,4-Dichloro-6-methylpyrimidine-5-carbonitrile is an efficient and inexpensive reagent for the synthesis of 2,6-dichloro-4-(trifluoromethyl)pyrimidine. It is a chlorinating agent that can be used in place of chlorine gas, which is expensive. The methylation reaction proceeds efficiently with n-butyl alcohol as the methylating agent, giving a high yield of product. The synthesis method has been shown to be effective for the preparation of this chemical.

Versatile small molecule scaffold

4-Phenyl-5-(pyridin-2-yl)-4H-1,2,4-triazole-3-thiol is a ligand that can be used to form supramolecular architectures. The compound has a coordination geometry of square pyramidal and exhibits anion recognition properties.

<p>1-Ethynyl-4-(methylsulfanyl)benzene (EMSB) is a novel organometallic compound that has been shown to be an inhibitor of cyclooxygenases. EMSB inhibits cox-1 and cox-2, which are enzymes involved in the inflammatory response. Inhibiting these enzymes may lead to the reduction of inflammation, which is implicated in many diseases such as cancer, arthritis, and cardiovascular disease. EMSB has also been shown to have antiinflammatory activity in a gravimetric analysis of human neutrophils. This molecule has been shown to inhibit the production of prostaglandins by inhibiting the enzyme cyclooxygenase and x-ray diffraction data show that this molecule binds with high affinity to cox-1 and cox-2.</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

2-(1,3-Benzothiazol-2-yl)-1-phenylethan-1-one is a selective cyclocondensation agent that can be used in the recycling of organic substances. It has been shown to efficiently catalyze intramolecular and intermolecular cyclocondensation reactions, as well as cleavage and disulfide formation. 2-(1,3-Benzothiazol-2-yl)-1-phenylethan-1-one has an intramolecular cyclocondensation activity with a variety of substrates, including benzene and ethylbenzene. This compound also has an intermolecular cyclocondensation activity with phenols, amines, and carboxylic acids. 2-(1,3-Benzothiazol-2-yl)-1-phenylethan-1-one is selectively active against secondary alcohols.

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Ethyl 2-chloro-2-(methylsulfanyl)acetate is a synthetic antiinflammatory agent that has been shown to be effective in the treatment of inflammation. Ethyl 2-chloro-2-(methylsulfanyl)acetate is chemically related to butyric acid and ibuprofen, which are both natural antiinflammatory agents. It inhibits the production of prostaglandins, which may be responsible for the antiinflammatory effects. The synthesis of ethyl 2-chloro-2-(methylsulfanyl)acetate begins with an acid chloride and a benzene ring. The condensation reaction forms an ester, which is then subjected to Friedel-Crafts reactions. This process produces phthalic anhydride and nitrated products.

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

2-[(Methylcarbamoyl)amino]acetic acid is a chemical compound that belongs to the group of amides. It is an intermediate in the synthesis of carbamic acid. The equilibrium constant for this reaction can be determined by the following scheme: In this scheme, the carboxylic acid protonates to form a carbamic acid anion, which reacts with ammonia to produce ammonium carbamate. This ammonium carbamate then undergoes hydrolysis to form 2-[(methylcarbamoyl)amino]acetic acid. 2-[(Methylcarbamoyl)amino]acetic acid has also been shown to have kinetic isotope effects, as it was found that hydrogen atoms from deuterium substituted at C3 and C4 positions have different reactivity than those from protium.

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

<p>Methyl 1,2-thiazole-4-carboxylate is a benzyl derivative that has been shown to have the ability to repair DNA. This compound is a pharmacological agent that has been shown to have anti-inflammatory and anti-tumour properties. Methyl 1,2-thiazole-4-carboxylate is also an inhibitor of alkyltransferase and inactivates purines and guanines. It is metabolized by the enzyme methyltransferase which modifies it to methyl 2,3-thiazole carboxylate. The stereochemistry of this molecule can be determined by focusing on the methyl group on carbon number 2 or 3.</p>

<p>Versatile small molecule scaffold</p>

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>4-Bromo-N-(dimethyloxido-λ4-sulfanylidene)benzenamine is a pandemic influenza drug that has been shown to have antiviral activity against the H1N1 virus. Covid-19, the active ingredient in 4-Bromo-N-(dimethyloxido-λ4-sulfanylidene)benzenamine, is a nucleoside analog that inhibits viral replication by blocking the interaction between viral RNA polymerase and host cell ribosomes. Covid-19 has been shown to be effective against laboratory strains of H1N1 and H3N2 influenza A viruses and is currently undergoing clinical trials. Covid-19 also has antiviral activity against other respiratory viruses such as SARS coronavirus and human metapneumovirus.</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>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<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>

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>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>

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.

Versatile small molecule scaffold

<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>

Versatile small molecule scaffold

<p>Versatile small molecule scaffold</p>

Versatile small molecule scaffold

Versatile small molecule scaffold

Versatile small molecule scaffold

<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>

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

Versatile small molecule scaffold

Versatile small molecule scaffold

<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>

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>

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.

Versatile small molecule scaffold

Versatile small molecule scaffold

<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>