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2,11-diaza[3.3]paracyclophane is a heterocyclic organic compound characterized by its unique structure, which consists of a paracyclophane framework with two nitrogen atoms incorporated into the molecule. 2,11-diaza[3.3]paracyclophane is a member of the aza-paracyclophane family, which are known for their potential applications in various fields, such as supramolecular chemistry and catalysis. The presence of nitrogen atoms in the structure of 2,11-diaza[3.3]paracyclophane contributes to its distinct electronic properties and reactivity compared to its carbon-only analogs. The compound's cyclic nature and the incorporation of nitrogen atoms make it an interesting subject for research, as it can potentially form stable complexes with metal ions and participate in various chemical reactions.

7215-86-3

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7215-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7215-86-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,1 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7215-86:
(6*7)+(5*2)+(4*1)+(3*5)+(2*8)+(1*6)=93
93 % 10 = 3
So 7215-86-3 is a valid CAS Registry Number.

7215-86-3Downstream Products

7215-86-3Relevant academic research and scientific papers

Self-Assembly of a Au16 ring via metal-metal bonding interactions

Wang, Ya-Qing,Li, Hao,Yu, Shu-Yan,Jiang, Xuan-Feng

, p. 1146 - 1149 (2015/08/26)

Metal-metal bonding interactions have been employed as an efficient strategy to generate a number of unique gold(I) metallo-macrocycles with fascinating functions. The self-assembly, crystal structure and emission property of novel nest-like tetramer 1su

A simple synthetic method for tetraaza[3.3.3.3]meta- and paracyclopanes by alkylation of N-substituted trifluoroacetamide

Shinmyozu,Shibakawa,Sugimoto,Sakane,Takemura,Sako,Inazu

, p. 1257 - 1260 (2007/10/02)

A simple and practical synthesis of the title compounds 1b and 2b is described. Alkylation of N-substituted trifluoroacetamides (5a and b) with appropriate dibromides (6 and 9) in the presence of sodium hydride in N,N-dimethylformamide at 100°C, or powder

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