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Bicyclo[4.1.0]heptane, 7,7-dichloro-1-phenyl- is a chemical compound with the molecular formula C13H14Cl2. It is a derivative of bicyclo[4.1.0]heptane, a bicyclic hydrocarbon with a seven-membered ring. The compound features two chlorine atoms attached to the 7th carbon position and a phenyl group (C6H5) attached to the 1st carbon position. This organic compound is known for its unique structure and potential applications in various chemical reactions and synthesis processes. It is important to note that the compound's properties, such as reactivity and solubility, may be influenced by the presence of the chlorine atoms and the phenyl group.

1796-39-0

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1796-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1796-39-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,9 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1796-39:
(6*1)+(5*7)+(4*9)+(3*6)+(2*3)+(1*9)=110
110 % 10 = 0
So 1796-39-0 is a valid CAS Registry Number.

1796-39-0Downstream Products

1796-39-0Relevant academic research and scientific papers

Thiocarbonyl Surrogate via Combination of Sulfur and Chloroform for Thiocarbamide and Oxazolidinethione Construction

Tan, Wei,Wei, Jianpeng,Jiang, Xuefeng

supporting information, p. 2166 - 2169 (2017/04/27)

An efficient and practical thiocarbonyl surrogate via combination of sulfur and chloroform has been developed. A variety of thiocarbamides and oxazolidinethiones have been established, including chiral thiourea catalysts and chiral oxazolidinethione auxiliaries with high selectivity. Meanwhile, pesticides Diafenthiuron (an acaricide), ANTU (a rodenticide), and Chloromethiuron (an insecticide) were practically synthesized through this method in gram scale. Dicholorocarbene, as the key intermediate, was further confirmed via a carbene-trapping control experiment.

Synthesis and Ring Cleavage of Highly Substituted 1,1-Dichloro- and 1-Bromo-1-fluorocyclopropanes

Anke, Lutz,Reinhard, Detlef,Weyerstahl, Peter

, p. 591 - 602 (2007/10/02)

The tri- and tetrasubstituted olefines 1, 2, 4, 7 - 15, and 19 react with CCl2 to give the dichlorocyclopropanes 22, 23, 25, 26a - 30a, and 33a - 37a in high yield, while the highly sterically hindered olefins 5, 6, and 21 show no reaction.In a few border

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