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| Product | Description | |
|---|---|---|
| Flumazenil Related Compound A | Flumazenil Related Compound A is an impurity of Flumazenil. Synonyms: 8-Fluoro-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid; Flumazenil acid; 4H-Imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid, 8-fluoro-5,6-dihydro-5-methyl-6-oxo-; O-Desethylflumazenil; 3-Desethyl-FMZ; Ro 15-3890. Grades: > 95%. CAS No. 84378-44-9. Molecular formula: C13H10FN3O3. Mole weight: 275.24. |  |
| Flumazenil Related Compound B | Flumazenil Related Compound B is an impurity of Flumazenil. Synonyms: 4H-Imidazo[1,5-a][1,4]benzodiazepine-3-carboxylicacid, 5,6-dihydro-8-hydroxy-5-methyl-6-oxo-, ethyl ester; Ethyl 8-hydroxy-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate; Defluoro 8-Hydroxy Flumazenil (Impurity) ; 5,6-Dihydro-. Grades: > 95%. CAS No. 131666-45-0. Molecular formula: C15H15N3O4. Mole weight: 301.30. | |
| N,N-Dimethylformamide diethyl acetal | Flumazenil Related Compound C is used as a reagent in the design of EGF-R tyrosine kinase inhibitors. lt was used in quantification of cocaine and its primary metabolite, benzoyl ecgonine from urine matrix by gas chromatography. Uses: N,n-dimethylformamide diethyl acetal is used as a reagent in the design of egf-r tyrosine kinase inhibitors. also used in the synthesis of aminopyridine derivatives. Synonyms: 1,1-diethoxy-N,N-dimethylmethanamine. Grades: > 95 %. CAS No. 1188-33-6. Molecular formula: C7H17NO2. Mole weight: 147.22. | |
| Perfluoro-1-iodohexane | Bretazenil (Ro16-6028) is an imidazopyrrolobenzodiazepine anxiolytic drug that is derived from the benzodiazepine family and was invented in 1988. It is most closely related in structure to the benzodiazepine antagonist flumazenil, although its effects are somewhat different. It is classed as a high-potency benzodiazepine due to its high-affinity binding to benzodiazepine binding sites where it acts as a partial agonist. Its profile as a partial agonist and preclinical trial data suggests that it may have a reduced adverse effect profile. In particular, bretazenil has been proposed to cause a less strong development of tolerance and withdrawal syndrome. Bretazenil differs from traditional 1,4-benzodiazepines by being a partial agonist and because it binds to α1, α2, α3, α4, α5, and α6 subunit-containing GABAA receptor benzodiazepine receptor complexes. 1,4-benzodiazepines bind only to α1, α2, α3 and α5 GABAA benzodiazepine receptor complexes. Group: Heterocyclic organic compound. Alternative Names: Tridecafluoro-1-iodohexane;PERFLUORO-N-HEXYL IODIDE; 1-Iodotridecafluorohexane; Perfluorohexyl iodide;1-iodo-tridecafluoro-hexane. CAS No. 355-43-1. Molecular formula: C6F13I. Mole weight: 445.95. Appearance: Liquid. Purity: 98. Density: 2.063. Catalog: ACM355431. |  |
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