Aminoácidos (AA)

Applications Isotope labelled 2-Bromo-4-methoxy-6-methylpyrimidine is a chemical reagent used in the preparation and synthesis of novel thiadiazoles and their derivatives for their growth stimulant activity.
References Knyazyan, A. et al.: J. Hetero. Chem., 50, 1281 (2013);

Applications 4-[N-Ethyl-(4-methoxyphenyl)methylamino]-2-butynyl-1-ol (cas# 181647-06-3) is a compound useful in organic synthesis.

Applications 2-Methyl-4-oxo-4-phenylbutyric Acid is a chemical reagent used in the synthesis of various pharmaceutically active compounds. Used in the synthesis of Minozac, a suppressor of brain proinflammatory cytokine up-regulation.
References Hu, W. et al.: Bioog. Med. Chem. Lett., 17, 414 (2007); Qabaja, G. ET AL.: J. ORG. CHEM., 80, 133 (2015);

Applications N-Methylisoamylamine is a reagent used in the synthesis of hepatitis C polymerase inhibitors.
References Cheng, C. et al: Bioorg.

Applications 1-(chloroacetyl)-4-methylpiperazine (cas# 40340-73-6) is a useful research chemical.

Applications Ethyl 2-chloro-2-(2-(4-methoxyphenyl)hydrazono)acetate (cas# 27143-07-3) is a useful research chemical.

Applications 2-Methyl-6-nitroaniline (cas# 570-24-1) is a compound useful in organic synthesis. Dyes and metabolites, Environmental Testing
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

Applications Tetrahydro-5-methyl-2-furanmethanol, is shown to be one of the volatile components in grapes, milk, and etc.
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 Mentasti, T., et al.: Milchwissenchaft, 52, 253 (1997);

Applications o-Coumaric Acid 4-O-β-D-Glucuronide is a metabolite of either Coumarin (C755380) or o-Hydroxy-cinnamic Acid (614-60-8).

Applications tert-Butoxycarbonyl-D-valine is used in the preparation of selective CCR1 antagonists in the treatment of rheumatoid arthritis. Also used in the preparation of antileishmanial agents.
References Gardner, D. et al.: Bioorg. Med. Chem. Lett., 23, 3833 (2013); Casanova, E. et al.: ChemMedChem., 8, 1161 (2013);