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N-(4-cyanophenyl)-3-phenylpropanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24722-24-5

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24722-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24722-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,2 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24722-24:
(7*2)+(6*4)+(5*7)+(4*2)+(3*2)+(2*2)+(1*4)=95
95 % 10 = 5
So 24722-24-5 is a valid CAS Registry Number.

24722-24-5Relevant academic research and scientific papers

Practical one-pot amidation of N -Alloc-, N -Boc-, and N -Cbz protected amines under mild conditions

Hong, Wan Pyo,Tran, Van Hieu,Kim, Hee-Kwon

, p. 15890 - 15895 (2021/05/19)

A facile one-pot synthesis of amides from N-Alloc-, N-Boc-, and N-Cbz-protected amines has been described. The reactions involve the use of isocyanate intermediates, which are generated in situ in the presence of 2-chloropyridine and trifluoromethanesulfonyl anhydride, to react with Grignard reagents to produce the corresponding amides. Using this reaction protocol, a variety of N-Alloc-, N-Boc-, and N-Cbz-protected aliphatic amines and aryl amines were efficiently converted to amides with high yields. This method is highly effective for the synthesis of amides and offers a promising approach for facile amidation.

Intermediate formation enabled regioselective access to amide in the Pd-catalyzed reductive aminocarbonylation of olefin with nitroarene

Li, Fuwei,Shi, Lijun,Xia, Chungu,Yang, Li

, p. 1152 - 1160 (2020/03/13)

An efficient route for the palladium-catalyzed reductive aminocarbonylation of olefins with nitroarenes was developed using carbon monoxide (CO) as both reductant and carbonyl source, which enables facile access to amides with excellent regioselectivity a

Synthesis of Acetaminophen Analogues Containing α-Amino Acids and Fatty Acids for Inhibiting Hepatotoxicity

Imai, Nobuyuki,Jung, Seunghee,Kawashima, Yuya,Noguchi, Takuya

, p. 3686 - 3696 (2019/09/30)

Acetaminophen is a popular antipyretic analgesic medicine that has weaker anti-inflammatory properties and lower incidence of side effects than nonsteroidal anti-inflammatory drugs (NSAIDs). However, acetaminophen causes hepatotoxicity due to the reactive metabolite N -acetyl- p -benzoquinone imine (NAPQI). We have obtained acetaminophen analogues in 57-99percent yields by using aniline derivatives with protected α-amino acids and fatty acids via the corresponding mixed carbonic carboxylic anhydrides in aqueous MeCN. We have also succeeded in synthesizing AM404 analogues in 76-97percent yields, which are expected to be promising candidates for reducing hepatotoxicity.

A Practical and General Amidation Method from Isocyanates Enabled by Flow Technology

Williams, Jason D.,Kerr, William J.,Leach, Stuart G.,Lindsay, David M.

supporting information, p. 12126 - 12130 (2018/09/11)

The addition of carbon nucleophiles to isocyanates represents a conceptually flexible and efficient approach to the preparation of amides. This general synthetic strategy has, however, been relatively underutilized owing to narrow substrate tolerance and the requirement for less favourable reaction conditions. Herein, we disclose a high-yielding, mass-efficient, and scalable method with appreciable functional group tolerance for the formation of amides by reaction of Grignard reagents with isocyanates. Through the application of flow chemistry and the use of substoichiometric amounts of CuBr2, this process has been developed to encompass a broad range of substrates, including reactants found to be incompatible with previously published procedures.

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