More research is needed about 1,4-Bis(benzo[d]oxazol-2-yl)naphthalene

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The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature. 5089-22-5, Name is 1,4-Bis(benzo[d]oxazol-2-yl)naphthalene, SMILES is C1(C2=NC3=CC=CC=C3O2)=C4C=CC=CC4=C(C5=NC6=CC=CC=C6O5)C=C1, in an article , author is Abu-Melha, Sraa, once mentioned of 5089-22-5, Safety of 1,4-Bis(benzo[d]oxazol-2-yl)naphthalene.

Synthesis and Biological Evaluation of Some Novel 1,8-Naphthyridine Derivatives

A series of substituted 1,8-naphthyridine derivatives was synthesized to be used as cytotoxic and antioxidant agents by applying 1,4-dihydro-4-oxo-1,8-naphthyridine-3-carbohydrazide (1) as the starting material. Compound 1 was reacted with different reagents to afford the corresponding 3-heterarylcarbonyl-1,8-naphthyridine derivatives 3-19 which were tested for their in vitro cytotoxicity against Ehrlich Ascites Carcinoma, and antioxidant activity. Compound 15 showed the best cytotoxicity and antioxidant activity.

Interested yet? Read on for other articles about 5089-22-5, you can contact me at any time and look forward to more communication. Safety of 1,4-Bis(benzo[d]oxazol-2-yl)naphthalene.

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