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The chemical "4,5,6,7,8,8-hexachloro-2-propoxy-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione" is a complex organic compound with a molecular formula of C12H8Cl6NO3. It is characterized by the presence of six chlorine atoms, a propoxy group, and a tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione structure. 4,5,6,7,8,8-hexachloro-2-propoxy-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione is known for its potential use as a pesticide, specifically as a miticide, which targets mites that can be harmful to agriculture. Its chemical structure provides it with the ability to disrupt the nervous systems of these pests, making it an effective tool in pest control. However, due to its complex nature and potential environmental impacts, it is important to handle and use such chemicals with care and in accordance with safety regulations.

6655-34-1

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6655-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6655-34-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,5 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6655-34:
(6*6)+(5*6)+(4*5)+(3*5)+(2*3)+(1*4)=111
111 % 10 = 1
So 6655-34-1 is a valid CAS Registry Number.

6655-34-1Relevant academic research and scientific papers

Silver-Catalyzed Cross-Olefination of Donor and Acceptor Diazo Compounds: Use of N-Nosylhydrazones as Diazo Surrogate

Liu, Zhaohong,Liu, Binbin,Zhao, Xue-Feng,Wu, Yan-Bo,Bi, Xihe

supporting information, p. 928 - 932 (2017/02/15)

The cross-olefination reaction of donor and acceptor diazo compounds was explored. The use of N-nosylhydrazones as diazo surrogates and the dependence on silver catalysis were crucial for the reaction development. A variety of (hetero)aryl N-nosylhydrazones and α-diazo esters, amides, and phosphonates were compatible, and the functionalized alkene products were afforded in good to high yields with moderate (Z)/(E) selectivities. The experimental and DFT calculation results suggest that the cross-selectivity is due to selective activation of the silver catalyst for donor diazo compounds.

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