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1,3-Benzenedicarbonitrile, 4,5,6-trichloro-2-hydroxy- is a chemical compound with the molecular formula C8H2Cl3N2O. It is a derivative of benzene, featuring two cyano groups (-CN) at the 1 and 3 positions, a hydroxyl group (-OH) at the 2 position, and three chlorine atoms at the 4, 5, and 6 positions. 1,3-Benzenedicarbonitrile, 4,5,6-trichloro-2-hydroxy- is known for its unique structure and properties, which can be utilized in various chemical reactions and applications. Due to its complex structure, it is essential to handle 1,3-Benzenedicarbonitrile, 4,5,6-trichloro-2-hydroxy- with care, as it may have potential health and environmental impacts.

30757-52-9

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30757-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30757-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,5 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 30757-52:
(7*3)+(6*0)+(5*7)+(4*5)+(3*7)+(2*5)+(1*2)=109
109 % 10 = 9
So 30757-52-9 is a valid CAS Registry Number.

30757-52-9Downstream Products

30757-52-9Relevant academic research and scientific papers

Synthesis and antiinflammatory evaluation of substituted isophthalonitriles, trimesonitriles, benzonitriles, and terephthalonitriles

Heilman,Battershell,Pyne,Goble,Magee

, p. 906 - 913 (2007/10/06)

In an effort to develop nonacidic, nonsteroidal, antiinflammatory agents without gastrointestinal complications, a series of cyanobenzenes was synthesized for antiinflammatory evaluation. Twenty-seven substituted isophthalonitriles, 19 trimesonitriles, 30 benzonitriles, and 16 terephthalonitriles were tested in the rat utilizing the carrageenan-induced pedal edema assay. Based on the performance of phenylbutazone in this assay (43.8% reduction at 100 mg/kg), six compounds, dosed at 50 mg/kg, produced reductions in inflammation comparable to this standard. However, the LD50 value of each compound dosed at this level was in the range of 40-56 mg/kg in the mouse; therefore, further study was not warranted. Fifteen compounds possessed activity in excess of 20% reduction at 200 mg/kg and also possessed LD50 values greater than 300 mg/kg. Of these cyanobenzenes, trimesonitrile, 4-chlorobenzonitrile, 2-chloroterephthalonitrile, and 2-fluoroterephthalonitrile with reductions in edema of 32, 30, 46, and 49%, respectively, represent the best candidates for subsequent study.

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