Archives for Chemistry Experiments of 5959-52-4

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 5959-52-4. Safety of 3-Amino-2-naphthoic acid.

Chemistry, like all the natural sciences, Safety of 3-Amino-2-naphthoic acid, begins with the direct observation of nature¡ª in this case, of matter.5959-52-4, Name is 3-Amino-2-naphthoic acid, SMILES is NC1=CC2=C(C=CC=C2)C=C1C(O)=O, belongs to naphthyridines compound. In a document, author is Mogilaiah, K., introduce the new discover.

Green synthesis, antibacterial and anti-inflammatory activities of 2-(2-substituted[1,8]naphthyridin-3-yl)-5-(substituted-2-thienyl)-1,3,4-oxadiazoles

An efficient and mild method for the synthesis of 2-(2-substituted[1,8]naphthyridin-3-yl)-5-(substituted-2-thienyl)-1,3,4-oxadiazoles 4 is reported by the oxidation of the corresponding N’3-[1-(substituted-2-thienyl)methylidene]-2-sustituted[1,8]naphthyridine-3-carbohydrazides 3 with iodobenzene diacetate(PhI(OAc)(2)] in solid state. The reaction proceeds efficiently giving the products in good yields and excellent purities. The structural assignments of compounds 3 and 4 are based on their elemental analyses and spectral (IR, H-1 NMR and MS) data. The compounds 4 have been screened for their antibacterial and anti-inflammatory activities.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 5959-52-4. Safety of 3-Amino-2-naphthoic acid.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem