Top Picks: new discover of 581-96-4

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield. If you are hungry for even more, make sure to check my other article about 581-96-4, Application In Synthesis of 2-(Naphthalen-2-yl)acetic acid.

You could be based in a university, combining chemical research with teaching; working on developing and trialing new drugs; or helping to ensure national healthcare provision keeps pace with new discoveries. 581-96-4, Name is 2-(Naphthalen-2-yl)acetic acid, molecular formula is C12H10O2, belongs to isothiazole compound. In a document, author is STRATMANN, K, introduce the new discover, Application In Synthesis of 2-(Naphthalen-2-yl)acetic acid.

Aulosirazole, the major cytotoxin in the blue-green alga (cyanobacterium) Aulosira fertilissima Ghose (UH strain DO-8-1), shows solid tumor selective activity in the Corbett assay. Its structure has been determined to be 5-hydroxy-3-methoxynaphtho[2,3-d]-1,2-thiazole-4,9-dione by a combination of spectroscopic, notably NMR, and X-ray crystallographic methods. The carbon skeleton and the juglone nature of 1 was determined by two-dimensional H-1-C-13 NMR correlation spectral analysis and one-dimensional C-13-C-13 decoupling experiments, the latter on the C-13-enriched cytotoxin. The presence of an isothiazole ring and the position of attachment for the juglone system was rigorously established by an X-ray crystallographic study.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield. If you are hungry for even more, make sure to check my other article about 581-96-4, Application In Synthesis of 2-(Naphthalen-2-yl)acetic acid.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com