Building Blocks

Applications 1-Phenyl-1,2,3,4-tetrahydroisoquinoline is a Solifenacin (S676700) intermediate. 1-Phenyl-1,2,3,4-tetrahydroisoquinoline had been detected in parkinsonian human brain. 1-Phenyl-1,2,3,4-tetrahydroisoquinoline maybe a candidate for endogenous MPTP-like neurotoxin since it is a structural analogue of MPTP which produces parkinsonism in humans.
References Kajita, M. et al.: J. Chrom. B Biomed. Appl., 669, 345 (1995);

Applications 1-Bromo-3-methylbutane, is used as an extraction solvent to determine various polycyclic aromatic hydrocarbons in water samples though dispersive liquid-liquid microextraction along with GC-MS (gas chromatography- mass spectrometry).
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Rezaee, M., et al.: J. Chromat. A., 1116, 1 (2006)

Applications Methyl 4-Chloropicolinate (cas# 24484-93-3) is a compound useful in organic synthesis.

Applications Pramoxine impurity. Phenol derivatives induced tumor cell apoptosis.
References Li, B., et al.: J. Biochem., 138, 679 (2005), Peltason, L., et al.: J. Med. Chem., 50, 5571 (2007),

Applications A chemical additive to control bacterial contamination in ethanol fermentation.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Vaisanen, O., et al.: J. Ind. Microbio., 4, 419 (1989), Costerton, J., et al.: J. Bacteriol., 176, 2137 (1994), Pirttijarvi, T., et al.: J. Appl. Bacteriol., 81, 445 (1996),

Impurity Solifenacin EP impurity A
Applications Solifenacin (S676700) intermediate.
References Andersson, K., et al.: Drugs, 35, 477 (1988), Wallis, R., et al.: Life Sci., 64, 395 (1999), Mitsuya, M., et al.: J. Med. Chem., 43, 5017 (2000), Ohtake, A., et al.: Eur. J. Pharmacol., 492, 243 (2004),

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.

2'-Methoxyacetophenone is a member of the class of halogenated phenols that exhibits anti-inflammatory activities. It inhibits protease activity in vitro and has been shown to have anti-inflammatory effects in vivo. 2'-Methoxyacetophenone is a ruthenium complex with hydrochloride salt that has been shown to be an efficient catalyst for acylation reactions. This compound also inhibits the transfer of the nerve impulse from the trigeminal nerve to the brain, which may be due to its ability to inhibit lipid peroxidation and protein autoxidation. 2'-Methoxyacetophenone has also been shown to have antimicrobial activity against gram-negative bacterial species, such as Proteus vulgaris, Escherichia coli, Pseudomonas aeruginosa, and Salmonella enterica.

Methyl 4-aminobenzoate is a chemical compound that is used as a fluorescence probe in the study of DNA replication. It can be used to detect the presence of viral RNA in cell culture, and has been shown to inhibit the replication of bacterial RNA. Methyl 4-aminobenzoate binds to guanine residues in DNA and forms an alkyl bond with them. This prevents the binding of other amino acids, which are essential for DNA replication. Methyl 4-aminobenzoate has also been shown to have pharmacokinetic properties that make it useful for intravenous administration and oral administration.