3808-87-5 Usage
Description
Bis(2,4,5-trichlorophenyl) disulfide is a chlorinated aromatic compound consisting of two phenyl groups, each with three chlorine atoms, connected to a sulfur atom. It is known for its strong antimicrobial and antifungal properties, making it a potential candidate for use as a pesticide and fungicide.
Uses
Used in Pesticide Industry:
Bis(2,4,5-trichlorophenyl) disulfide is used as a pesticide for its strong antimicrobial and antifungal properties, helping to protect crops from various pests and diseases.
Used in Fungicide Industry:
In the fungicide industry, Bis(2,4,5-trichlorophenyl) disulfide serves as an effective antifungal agent, preventing the growth of fungi that can cause damage to plants and reduce crop yields.
However, it is important to note that Bis(2,4,5-trichlorophenyl) disulfide is classified as a persistent organic pollutant and has been shown to have toxic effects on aquatic organisms. Its potential to bioaccumulate and harm the environment has led to international regulations and restrictions on its use and production. Understanding the structure and properties of this chemical is crucial for assessing its potential impact on human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 3808-87-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,0 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3808-87:
(6*3)+(5*8)+(4*0)+(3*8)+(2*8)+(1*7)=105
105 % 10 = 5
So 3808-87-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H4Cl6S2/c13-5-1-9(17)11(3-7(5)15)19-20-12-4-8(16)6(14)2-10(12)18/h1-4H
3808-87-5Relevant articles and documents
Synthesis of Disulfides from the Palladium(0)-Catalyzed Reactions of Sulfenyl Halides and Organostannanes
Cochran, John C.,Friedman, Susan R.,Frazier, John P.
, p. 1533 - 1536 (2007/10/03)
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Thioxanthene derivatives of pharmacological interest: 1,2,4-trichloro and 2,4,5,6-tetrachloro derivatives of 9-(3-dimethylaminopropylidene)thioxanthene
Bartl,Kmonicek,Sedivy,et al.
, p. 2295 - 2308 (2007/10/02)
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REACTION OF N,N'-THIONYLDIIMIDAZOLE WITH THIOLS: A SULFUR TRANSFER REACTION
Ogata, Masaru,Matsumoto, Hiroshi,Shimizu, Sumio
, p. 955 - 958 (2007/10/02)
Reaction of N,N'-thionyldiimidazole with thiols effects the formation of disulfides and trisulfides.These results are rationalized by assuming that the thiols react with N,N'-thionyldiimidazole to produce the disulfides and N,N'-thiobisimidazole which subsequently reacts with the starting thiols to give the trisulfides.
