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1-(3-chlorophenyl)tricyclo[3.3.1.1^3,7^]decane is a complex organic compound with a unique tricyclic structure. It consists of three fused rings, with the central ring being a cyclohexane ring, and the two side rings being cyclopropane rings. The compound features a 3-chlorophenyl group attached to the first carbon atom of the central cyclohexane ring. This chlorophenyl group introduces a halogen atom, which can significantly alter the compound's reactivity and properties compared to its non-halogenated analogs. The compound's molecular formula is C15H19Cl, and it has a molecular weight of approximately 232.77 g/mol. Due to its complex structure and potential reactivity, 1-(3-chlorophenyl)tricyclo<3.3.1.13,7>decane may have applications in various fields, such as pharmaceuticals or materials science, where its unique properties can be exploited.

59974-39-9

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59974-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59974-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,7 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59974-39:
(7*5)+(6*9)+(5*9)+(4*7)+(3*4)+(2*3)+(1*9)=189
189 % 10 = 9
So 59974-39-9 is a valid CAS Registry Number.

59974-39-9Downstream Products

59974-39-9Relevant academic research and scientific papers

Direct Clay-Catalyzed Friedel-Crafts Arylation and Chlorination of the Hydrocarbon Adamantane

Chalais, Stephane,Cornelis, Andre,Gerstmans, Andre,Kolodziejski, Waclaw,Laszlo, Pierre,et al.

, p. 1196 - 1203 (2007/10/02)

Multiple chlorinations and arylations at the tertiary positions of adamantane are promoted by FeCl3-doped K10 montmorillonite in CCl4 or in aromatic solvents.The process, remarkably easy implement, can be tailored to selective formation of monosubstituted 1-adamantyl derivatives or 1,3-disubstituted adamantanes.The process achieves alkylation at the meta- and para-positions of toluene leading to a purely statistical distribution and displays no substrate specificity in competition experiments between toluene and benzene.

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