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2,3-Diazabicyclo[2.2.1]heptane-2-carbonitrile, 3-(4-benzoylphenyl)is a bicyclic amine chemical compound that features a carbonitrile group and a 4-benzoylphenyl substituent. It is known for its utility in organic synthesis, particularly as a nucleophilic catalyst in various reactions. This versatile chemical has garnered interest for its potential applications in the pharmaceutical industry and beyond.

143262-45-7

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143262-45-7 Usage

Uses

Used in Organic Synthesis:
2,3-Diazabicyclo[2.2.1]heptane-2-carbonitrile, 3-(4-benzoylphenyl)is used as a nucleophilic catalyst for facilitating various organic reactions, enhancing the efficiency and selectivity of the processes involved.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2,3-Diazabicyclo[2.2.1]heptane-2-carbonitrile, 3-(4-benzoylphenyl)is utilized as a key component in the development of new drug molecules, contributing to the advancement of medicinal chemistry.
Used in Synthesis of Heterocyclic Compounds:
2,3-Diazabicyclo[2.2.1]heptane-2-carbonitrile, 3-(4-benzoylphenyl)is employed as a synthetic intermediate in the preparation of heterocyclic compounds, which are important in various fields, including pharmaceuticals and materials science.
Used in Metal-Catalyzed Reactions:
2,3-Diazabicyclo[2.2.1]heptane-2-carbonitrile, 3-(4-benzoylphenyl)is used as a ligand in metal-catalyzed reactions, playing a crucial role in the activation and selectivity of these catalytic processes.

Check Digit Verification of cas no

The CAS Registry Mumber 143262-45-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,6 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 143262-45:
(8*1)+(7*4)+(6*3)+(5*2)+(4*6)+(3*2)+(2*4)+(1*5)=107
107 % 10 = 7
So 143262-45-7 is a valid CAS Registry Number.

143262-45-7Downstream Products

143262-45-7Relevant academic research and scientific papers

Benzimidazolo-diazepines from 1,3-dienes and arenediazocyanides through a 1,3,4-tri-aza-Cope rerrangement

Rousselle, Daniel,Ryckmans, Thomas,Viehe, Heinz G.

, p. 5249 - 5258 (2007/10/02)

Cyclic and bicyclic 1-cyano-2-arylhydrazines were prepared from arene diazocyanides and 1,3-dienes. Some of them rearrange at room temperature through a 1,3,4-tri-aza-Cope rearrangement, followed by an intramolecular cyclisation, to afford benzimidazolo-d

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