New explortion of 2,7-Dibromo-9H-fluoren-9-one

Reference of 14348-75-5, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 14348-75-5.

Reference of 14348-75-5, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C¨CH bond functionalisation has revolutionised modern synthetic chemistry. 14348-75-5, Name is 2,7-Dibromo-9H-fluoren-9-one, SMILES is C3=C2C1=C(C=C(Br)C=C1)C(C2=CC(=C3)Br)=O, belongs to phthalazines compound. In a article, author is Mohamadpour, Farzaneh, introduce new discover of the category.

Four-component clean process for the eco-friendly synthesis of 1H-pyrazolo [1,2-b]phthalazine-5,10-dione derivatives using Zn(OAc)(2)center dot 2H(2)O as an efficient catalyst under solvent-free conditions

An efficient and convenient zinc acetate dihydrate (Zn(OAc)(2)center dot 2H(2)O) catalyzed synthesis of 1H-pyrazolo[1,2-b]phthalazine-5,10-dione derivatives has been accomplished via one-pot four-condensation of phthalic anhydride, hydrazine monohydrate, aromatic aldehydes derivatives and malononitrile under solvent-free conditions. The notable advantages of the present procedure are: operational simplicity, eco-friendly, environmentally benign nature, low-cost and non-toxic catalyst, no necessity of chromatographic purification steps, short reaction times and good to high yields.

Reference of 14348-75-5, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 14348-75-5.

Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem