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4-(isopentylamino)benzonitrile is an organic chemical compound with the molecular formula C12H16N2. It is a derivative of benzonitrile, featuring an isopentylamine group attached to the para position of the benzene ring. 4-(isopentylamino)benzonitrile is characterized by its amine and nitrile functional groups, which contribute to its chemical reactivity and potential applications in various fields, such as pharmaceuticals and agrochemicals. The isopentyl group, a branched-chain alkyl group, provides steric hindrance and can influence the compound's physical properties and reactivity. 4-(isopentylamino)benzonitrile is a colorless to pale yellow solid, and its synthesis often involves the reaction of 4-aminobenzonitrile with isopentyl chloride or a related alkylating agent. Due to its potential applications, it is important to consider its safety, handling, and environmental impact.

4714-66-3

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4714-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4714-66-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,1 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4714-66:
(6*4)+(5*7)+(4*1)+(3*4)+(2*6)+(1*6)=93
93 % 10 = 3
So 4714-66-3 is a valid CAS Registry Number.

4714-66-3Downstream Products

4714-66-3Relevant academic research and scientific papers

Practical heterogeneous photoredox/nickel dual catalysis for C-N and C-O coupling reactions

Liu, Yi-Yin,Liang, Dong,Lu, Liang-Qiu,Xiao, Wen-Jing

, p. 4853 - 4856 (2019)

Efficient C-N and C-O coupling reactions of aryl halides with amines and alcohols have been developed by using the strategy of heterogeneous visible light photoredox and nickel dual catalysis. Obviously, the joint use of inexpensive and bench-stable CdS and nickel salts, together with mild reaction conditions, makes these two transformations attractive for the synthetic community. This heterogeneous dual catalysis system also proved to be successful in the ligand-free catalytic hydroxylation of aryl bromide with water as a nucleophile. The practicality of this protocol is further emphasized by the scaled-up reaction and the reusability of heterogeneous photocatalysts.

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