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N-cinnamylpyridin-2-amine is an organic compound with the chemical formula C16H16N2. It is a derivative of pyridin-2-amine, which is a heterocyclic aromatic compound containing a nitrogen atom in the pyridine ring. The molecule features a cinnamyl group (a propenylbenzene moiety) attached to the nitrogen atom of the pyridine ring, forming an amide linkage. N-cinnamylpyridin-2-amine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as a building block in the creation of more complex organic molecules. Due to its unique structure, N-cinnamylpyridin-2-amine may exhibit interesting chemical properties and reactivity, making it a subject of interest in organic chemistry research.

1212-55-1

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1212-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1212-55-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1212-55:
(6*1)+(5*2)+(4*1)+(3*2)+(2*5)+(1*5)=41
41 % 10 = 1
So 1212-55-1 is a valid CAS Registry Number.

1212-55-1Downstream Products

1212-55-1Relevant academic research and scientific papers

Nickel-catalyzed difunctionalization of allyl moieties using organoboronic acids and halides with divergent regioselectivities

Li, Wanfang,Boon, Jie Kang,Zhao, Yu

, p. 600 - 607 (2018)

Efficient difunctionalization of alkenes allows the rapid construction of molecular complexity from simple building blocks in organic synthesis. We present herein a nickel-catalyzed dicarbofunctionalization of alkenes using readily available organoboronic acids and organic halides in a three-component fashion. In particular, an unprecedented regioselectivity of the 1,3-dicarbofunctionalization of N-allylpyrimidin-2-amine is achieved when aryl and methyl iodides are utilized. In contrast, the use of alkyl bromides with β-hydrogens results in 1,3-hydroarylation or oxidative 1,3-diarylation. Preliminary mechanistic studies suggest an isomerization involving nickel hydride in the 1,3-difunctionalization reactions. On the other hand, the use of alkenyl or alkynyl halides promotes alternative regioselectivities to deliver 1,2-alkenylcarbonation or intriguing 2,1-alkynylcarbonation products. Such 2,1-alkynylarylation is also applicable to N-allylbenzamide as a different class of substrates. Overall, this nickel-catalyzed process proves to be powerful in delivering versatile difunctionalized compounds using readily available reagents/catalysts and a simple procedure.

Sulfonic acid supported on hydroxyapatite-encapsulated-γ-Fe 2O3 nanocrystallites as a magnetically separable catalyst for one-pot reductive amination of carbonyl compounds

Deng, Jia,Mo, Li-Ping,Zhao, Fei-Yang,Hou, Lan-Lan,Yang, Li,Zhang, Zhan-Hui

experimental part, p. 2576 - 2584 (2011/10/18)

A novel, environmentally friendly procedure has been developed for the preparation of secondary or tertiary amines by one-pot reductive amination of carbonyl compounds using sodium borohydride in the presence of a magnetically recoverable sulfonic acid supported on hydroxyapatite-encapsulated-γ- Fe2O3 [γ-Fe2O3@HAP-SO 3H] at room temperature. The catalyst was easily separated from the reaction mixture by applying an external magnet and reused for six cycles without significant loss of catalytic activity.

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