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N-(2,3,4,5,6-pentafluorophenyl)-3-phenylpropanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

425372-18-5

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425372-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 425372-18-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,5,3,7 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 425372-18:
(8*4)+(7*2)+(6*5)+(5*3)+(4*7)+(3*2)+(2*1)+(1*8)=135
135 % 10 = 5
So 425372-18-5 is a valid CAS Registry Number.

425372-18-5Relevant academic research and scientific papers

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.

Convenient synthesis of acetaminophen analogues containing α-amino acids and fatty acids via their mixed carbonic carboxylic anhydrides in aqueous organic solvent

Jung, Seunghee,Tsukuda, Yuki,Kawashima, Rie,Ishiki, Takumi,Matsumoto, Ayaka,Nakaniwa, Aya,Takagi, Miho,Noguchi, Takuya,Imai, Nobuyuki

, p. 5718 - 5720 (2013/09/24)

Acetaminophen analogues containing α-amino acid and fatty acids were easily synthesized in 77-99% yields from the corresponding mixed carbonic carboxylic anhydrides of α-amino acid and fatty acids using aniline derivatives in aqueous MeCN.

Amide-directed arylation of sp3 C-H bonds using Pd(II) and Pd(0) catalysts

Wasa, Masayuki,Yu, Jin-Quan

experimental part, p. 4811 - 4815 (2010/08/06)

Protocols to effect β-arylation of sp3 C-H bonds via Pd(II)/(IV) and Pd(0)/(II) catalytic cycles have been achieved using a newly developed monodentate CONHC6F5 directing group. These reactions provide an unprecedented means to functionalize sp3 C-H bonds in aliphatic carboxylic acid-derived substrates.

Pd(0)/PR3-catalyzed intermolecular arylation of sp3 C-H bonds

Wasa, Masayuki,Engle, Keary M.,Yu, Jin-Quan

supporting information; experimental part, p. 9886 - 9887 (2009/12/06)

(Figure Presented) Pd(0)-catalyzed intermolecular arylation of sp 3 C-H bonds has been achieved using PR3/Arl. This protocol can be used to arylate a variety of aliphatic carboxylic acid derivatives, including a number of bioactive d

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