Building Blocks

Plant hormone; auxin; inducer of root development; used in plant rooting

Versatile small molecule scaffold

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Tert-Butoxycarbonyl-L-leucine (tBOC-LL) is a tetrapeptide that is used as a drug substance in the synthesis of buserelin, a synthetic peptide hormone. It has been shown to have high reactivity in organic solvents and can be used in cationic polymerization reactions. tBOC-LL has been used to synthesize helical structures with high purity and yield. As it is not an amino acid, tBOC-LL does not occur naturally and must be synthesized.
Tert-Butoxycarbonyl-L-leucine (tBOC-LL) is available from Sigma Aldrich Chemie GmbH & Co KG as:

3-{[(Benzylsulfanyl)methanethioyl]sulfanyl}propanoic acid are essential mediators for reversible addition-fragmentation chain transfer (RAFT) polymerization, common type of controlled radical polymerization.

5-Amino-2-nitrobenzoic acid is an organic compound that belongs to the class of versatile building block. It is a white solid that has been used as a research chemical, reagent, and specialty chemical for the synthesis of complex compounds and pharmaceuticals. 5-Amino-2-nitrobenzoic acid is also known as 2-amino-5-chlorobenzoic acid (ACBA). It is soluble in water, but insoluble in ethanol. The CAS number for this chemical is 13280-60-9.

Versatile small molecule scaffold

Versatile small molecule scaffold

4-Acetoxyindole is a chromophore that belongs to the pyrrole family of compounds. It has been shown to react with an ionic liquid under acidic conditions to form a protonated intermediate, which can be deprotonated by a nucleophile. This reaction yields an acetate anion and a fluorescing product. 4-Acetoxyindole also reacts with deuterium gas, yielding an acetate, a deuterium atom, and fluorescing product. The reaction is reversible and the yield of the product depends on the concentration of the reactants. 4-Acetoxyindole has strong carbonyl groups that make it reactive towards other functional groups. These reactions are useful for synthesizing heterocycles such as indoles and isoquinolines.

3-Amino-adamantane-1-carboxylic hydrochloride is a versatile building block that can be used as a research chemical, reagent, speciality chemical, and useful scaffold in the synthesis of various complex compounds. It is a high quality intermediate and reaction component that can be used in the synthesis of fine chemicals. 3-Amino-adamantane-1-carboxylic hydrochloride has a variety of uses due to its versatility and can be used in the production of pharmaceuticals, agrochemicals, dyes, plastics, perfumes, pesticides, herbicides, explosives, and more.

Ruthenium complexes of 4-tert-butoxyphenylacetic acid are catalysts that have been shown to be effective in the asymmetric synthesis of alcohols and terpyridines.
This complex has been shown to be a ligand for ruthenium metal, which is often used as a catalyst in organic reactions. The use of this catalyst has led to advances in the field of organic chemistry, specifically the synthesis of new oligomers.

1-(Bromomethyl)adamantane is a synthetic chemical that is used in the preparation of other chemicals. The active site of 1-(bromomethyl)adamantane can be found on its bromine atom, which has been shown to react with copper. The regioselectivity is determined by the 1-position on adamantane, and the thermodynamic constants are affected by the carbon-halogen bond, which is present in 1-(bromomethyl)adamantane. This compound has been shown to have chromatographic properties that make it useful for separating compounds that are similar in structure. It can also be used as a reagent to synthesize other chemicals or prepare them for use in experiments.

2,6-Dimethoxy-4-propylphenol is an organic solvent that is used in the synthesis of pharmaceuticals and agricultural chemicals. It is also a precursor for lignin, a natural polymer found in plants. 2,6-Dimethoxy-4-propylphenol can be converted to 2,6-dimethoxyphenol by hydrolysis with water vapor or an acid catalyst. The skeleton of 2,6-dimethoxy-4-propylphenol is a carbon chain with ether linkages that are susceptible to hydrolysis reactions. These reactions produce monomers and fatty acids.

2,4,6-Trihydroxybenzophenone is a phenolic compound that has been shown to have significant inhibitory activities against the growth of bacteria in vitro. It can be used as a preservative for oils and fats. This product also inhibits the benzoate degradation pathway in E. coli and inhibits the synthesis of phenylpropanoids by inhibiting the activity of phenylalanine ammonia-lyase (PAL). 2,4,6-Trihydroxybenzophenone also has an inhibitory effect on cell proliferation and induces apoptosis in human leukemia cells. 2,4,6-Trihydroxybenzophenone belongs to the group of compounds called hypericins (hyperforin) that are produced by Hypericum perforatum plants. The biosynthesis of this molecule is thought to involve two consecutive hydroxylations at positions 4 and 6 on the aromatic ring.

7-Azaindole is a reactive chemical that has been shown to be effective in the treatment of skin cancer, as well as hepatic steatosis. The compound can promote the transfer of hydrogen atoms and form a dimer with protonated nitrogen. 7-Azaindole reacts rapidly with nucleophiles such as amines, alcohols, and thiols to form covalent bonds. The reaction mechanism is characterized by an initial protonation step followed by nucleophilic attack or hydrogen transfer from the nucleophile to 7-azaindole. Kinetic studies have demonstrated that the rate of this reaction depends on the concentration of both reactants.

4-Methoxybenzamide is a small molecule that has been shown to have anticancer activity in vitro and in vivo. It is a hydroxylated benzamide with an intramolecular hydrogen bond, which allows it to selectively bind to DNA at the C4' position of cytosine. The compound's anticancer effects are due to its ability to inhibit the transcription of genes involved in cancer cell proliferation and its ability to induce apoptosis via caspase activation. 4-Methoxybenzamide has been shown to be synergistic when used with other chemotherapeutics, such as cisplatin, doxorubicin or 5-fluorouracil. This drug also inhibits the uptake of these drugs by cancer cells, limiting their therapeutic effects on healthy tissues.

3-Ethoxy-4-hydroxybenzaldehyde is an active analogue of p-hydroxybenzoic acid that can be used in the synthesis of vanillin. 3-Ethoxy-4-hydroxybenzaldehyde is extracted from a reaction solution using solid phase microextraction, and can then be analyzed by gas chromatography/mass spectrometry to determine the concentration of vanillin. This compound has been shown to have a solubility in water, but not in organic solvents. 3-Ethoxy-4-hydroxybenzaldehyde has been found to inhibit cytochrome P450 activity and polyvinyl chloride production. This chemical compound has also been found to be toxic when inhaled or ingested, with no known toxicity studies for skin contact or eye contact.

6-Bromo-2-oxindole is a crystalline compound with a molecular formula of C10H6BrO. It has been shown to have a high efficiency in the production of butyric acid and other organic acids. 6-Bromo-2-oxindole is also used in electron microscopy studies as an electron acceptor, and can be used for producing polymers with crystalline structures and dihedral angles. The compound has been shown to inhibit the growth of breast cancer cells by preventing the synthesis of mda-mb-231 breast cancer cells. It also has been shown to inhibit the production of isoindigo and morphology.

3-Amino-2-hydroxybenzonitrile is a chemical that can be used as a building block in the synthesis of other compounds. It is also a versatile intermediate for organic synthesis and can be used for the production of pharmaceuticals, agrochemicals, and many other materials. 3-Amino-2-hydroxybenzonitrile is a white solid with a melting point of 203 degrees Celsius. It has high purity, low impurities, and a high quality.

Isatin is a natural compound that can be found in the bark of the Cinchona tree. It has inhibitory properties against the enzyme polymerase chain reaction (PCR) and has been shown to have antimicrobial activity. Isatin also has an effect on 5-HT concentrations, which may be due to its ability to inhibit platelet aggregation and induce vasoconstriction. Isatin has been shown to have anticancer effects in vitro, and also inhibits cellular transformation by reducing DNA synthesis.

2-Pyridinepropanol is a tetranuclear compound that contains two nitrogen atoms and two silver ions. It has been shown to be an inhibitor of arthropoda development in the laboratory. 2-Pyridinepropanol also has potent inhibitory activity against the growth of bacteria, including Staphylococcus aureus and Pseudomonas aeruginosa. This compound was synthesized from 2-benzoylbenzoic acid, which is a product of the plant metabolism. The structure of this molecule was determined by X-ray crystallography and electrochemical studies.
2-Pyridinepropanol binds to the bacterial enzyme hydrogenase, which catalyzes the production of hydrogen gas, thereby inhibiting its activity (hydrogenase is an enzyme that catalyses the reduction of protons to hydrogen gas).