Amino Acids (AA)

<p>Please enquire for more information about ethyl 5-methyl-3-(phenylamino)-2,4-thiazolecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 3-(4-Benzyloxy-3-methoxyphenyl)-4-methyl-1,2,4-triazoline-5-thione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Please enquire for more information about 4-phenyl-5-(4-(benzyloxy)phenyl)-1,2,4-triazole-3-thiol including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 3-(tert-Butyl)-2-methylindeno[3,2-c]pyrazol-4-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Please enquire for more information about 2-((4-Ethoxyphenyl)amino)-4-methyl-1,3-thiazole-5-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2,4-dimethoxy-1-(2-(1-methyl(2-pyridyl))vinyl)benzene, iodide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 1-(4-Nitrilophenyl)-3-(4-methylbenzoyl)thiourea including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

2-Chloro-N-(4-methoxyphenyl)acetamide is an antibacterial agent that binds to the bacterial ribosome and prevents protein synthesis. 2-Chloro-N-(4-methoxyphenyl)acetamide has been shown to be active against both Gram positive and negative bacteria, including methicillin resistant Staphylococcus aureus (MRSA), Enterococcus faecalis, Pseudomonas aeruginosa, and Klebsiella pneumoniae. The mechanism of action for 2-chloro-N-(4-methoxyphenyl)acetamide is not well understood, but it may involve binding to the ribosomal RNA in the bacterial cell. This binding blocks the formation of an antibiotic-ribosome complex that is required for translation of mRNA into protein.

<p>Please enquire for more information about ethyl 3-((2-fluorophenyl)amino)-5-methyl-2,4-thiazolecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about ethyl 3-((4-fluorophenyl)amino)-5-methyl-2,4-thiazolecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 1-(2-Aminobenzoyl)-4-phenylsemicarbazide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 4-Benzyloxy-3-methoxybenzoyl hydrazide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about N-(2-Methoxy-5-methylphenyl)-2-chloropropanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about Methyl 5-(((4-methylphenyl)sulfonyl)methyl)furan-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 5-Methyl-3-(4-phenylpiperazinyl)cyclohex-2-en-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Please enquire for more information about 2-((4-(Trifluoromethoxy)phenyl)amino)-4-methyl-1,3-thiazole-5-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,5-Dimethyl-1-phenylpyrrole is a colorless liquid that has been shown to undergo condensation reactions with chloride or nitro groups. 2,5-Dimethyl-1-phenylpyrrole can be synthesized by the reaction of phenylacetaldehyde and formaldehyde in the presence of an acid catalyst. This molecule also reacts with amines and provides a chromatographic technique for separating enantiomers. The functional groups present in this compound are electrophilic and nucleophilic, which are thermodynamically favorable. 2,5-Dimethyl-1-phenylpyrrole has been shown to react with ammonia gas at elevated temperatures, forming a molecule with nitro group. It has also been shown that 2,5-Dimethyl-1-phenylpyrrole can be used as an organic reagent for the synthesis of other molecules containing nitro group at room temperature.</p>

Please enquire for more information about 1-(2-Methyl(8-quinolyloxy))-2-nitro-4-(trifluoromethyl)benzene including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Please enquire for more information about Ethyl 3-(3-pyridylamino)-5-methyl-2,4-thiazolecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Please enquire for more information about N-(4-Fluoro-2-methylphenyl)-2-chloropropanamide including the price, delivery time and more detailed product information at the technical inquiry form on this page