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[(4-nitrophenyl)sulfonyl][(trifluoromethyl)sulfonyl]methane is a complex organic compound characterized by its molecular formula C9H5F3N2O7S2. [(4-nitrophenyl)sulfonyl][(trifluoromethyl)sulfonyl]methane features a central methane molecule, which is bonded to two sulfonyl groups: one is a 4-nitrophenyl sulfonyl group, and the other is a trifluoromethyl sulfonyl group. The 4-nitrophenyl sulfonyl group contains a nitro group attached to a phenyl ring, while the trifluoromethyl sulfonyl group has three fluorine atoms attached to a methyl group. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its reactivity and stability. It is also recognized for its ability to act as a protecting group in organic synthesis, particularly in the formation of esters and amides, where it can be used to temporarily block certain functional groups from reacting until the sulfonyl groups are removed under specific conditions.

734-24-7

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734-24-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 734-24-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,3 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 734-24:
(5*7)+(4*3)+(3*4)+(2*2)+(1*4)=67
67 % 10 = 7
So 734-24-7 is a valid CAS Registry Number.

734-24-7Relevant academic research and scientific papers

Synthesis and endectocidal activity of novel 1-(Arylsulfonyl)-1- [(trifluoromethyl)sulfonyl]methane derivatives

Wickiser, David I.,Wilson, Sharon A.,Snyder, Daniel E.,Dahnke, Karl R.,Smith II, Charles K.,McDermott, Paul J.

, p. 1092 - 1098 (2007/10/03)

We have recently synthesized a series of novel disulfonylmethane compounds that have shown anthelmintic and insecticidal (endectocidal) activity. Several analogues have shown activity against the internal nematode Haemonchus contortus. In sheep studies, these analogues have shown 100% control of this internal parasite at a 10 mg/kg rate. In vitro activity against the biting flies, Stomoxys calcitrans and Haematobia irritans, has been observed at rates as low as 25 and 2.3 ppm, respectively. Only marginal activity against the liver fluke Fasciola hepatica and Trichostrongylus colubriformis was seen. Respiratory control index values on rat liver mitochondria for this series suggested uncoupling of oxidative phosphorylation as a mechanism of action. Compound 1 is considered to be a promising agent for treatment of parasitized sheep.

Use of disulfonyl methanes for the control of parasites

-

, (2008/06/13)

The present invention is directed to the use of disulfonyl methane compounds for the control of parasites in vertebrate animals.

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