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1,3-Benzenedicarbonyl dichloride, 4,5,6-trichloro-2-fluoro- is a complex organic compound with the chemical formula C8Cl5F2O2. It is characterized by a benzene ring with two carbonyl groups (C=O) attached at the 1 and 3 positions, and three chlorine atoms and one fluorine atom substituting the 4, 5, 6, and 2 positions, respectively. 1,3-Benzenedicarbonyl dichloride, 4,5,6-trichloro-2-fluoro- is a derivative of phthalic anhydride, a common organic compound used in the production of plastics and resins. Due to its unique structure and properties, 1,3-Benzenedicarbonyl dichloride, 4,5,6-trichloro-2-fluoro- has potential applications in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. However, it is important to note that handling and disposal of 1,3-Benzenedicarbonyl dichloride, 4,5,6-trichloro-2-fluoro- should be done with caution, as it may have hazardous properties and require proper safety measures.

67324-68-9

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67324-68-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67324-68-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,2 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 67324-68:
(7*6)+(6*7)+(5*3)+(4*2)+(3*4)+(2*6)+(1*8)=139
139 % 10 = 9
So 67324-68-9 is a valid CAS Registry Number.

67324-68-9Relevant 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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