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2-(4-methylphenyl)benzofuran-3-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58491-52-4

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58491-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58491-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,9 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58491-52:
(7*5)+(6*8)+(5*4)+(4*9)+(3*1)+(2*5)+(1*2)=154
154 % 10 = 4
So 58491-52-4 is a valid CAS Registry Number.

58491-52-4Downstream Products

58491-52-4Relevant academic research and scientific papers

Preparation and application of 2-(4-substituted phenyl)-3-formamide benzofuranene cyanide compound

-

, (2019/04/17)

The invention provides a preparation and application of a 2-(4-substituted phenyl)-3-formamide benzofuranene cyanide compound. The benzofuranene cyanide compound shown in formula I has a structure shown in the following formula I, wherein the definition o

Construction of Benzofuran-3(2 H)-one Scaffolds with a Quaternary Center via Rh/Co Relay Catalyzed C-H Functionalization/Annulation of N-Aryloxyacetamides and Propiolic Acids

Yuan, Wen-Kui,Zhu, Ming-Hui,Geng, Rui-Sen,Ren, Guang-Yi,Zhang, Lin-Bao,Wen, Li-Rong,Li, Ming

supporting information, p. 1654 - 1658 (2019/03/11)

An unprecedented synthesis of valuable benzofuran-3(2H)-one scaffolds with a quaternary center was developed via Rh/Co relay catalyzed C-H functionalization/annulation of N-aryloxyacetamides with propiolic acids in moderate to good yields. The reaction features the simultaneous construction of the benzofuran motif containing a C2 quaternary center and a C3 carbonyl group. The preliminary mechanism study verified that the O atom of C3 carbonyl group originates from molecular oxygen.

Synthesis, biological evaluation and molecular docking analysis of 2-phenyl-benzofuran-3-carboxamide derivatives as potential inhibitors of Staphylococcus aureus Sortase A

He, Wan,Zhang, Yong,Bao, Jian,Deng, Xinxian,Batara, Jennifer,Casey, Shawn,Guo, Qiuyuan,Jiang, Faqin,Fu, Lei

, p. 1341 - 1351 (2017/02/18)

In Gram-positive bacteria, Sortase A (Srt A) is a critical cysteine transpeptidase that is responsible for recognizing and assembling surface virulence proteins through the recognition of a LPXTG (leucine, proline, X, threonine, and glycine, where X is an

Benzofuran compound, preparation method and applications thereof

-

, (2016/10/08)

The present invention provides a benzofuran compound, a preparation method and applications thereof, wherein the structure is represented by a general formula (I-1) or (I-2), R1, R3 and R4 are any one selected from hydrogen, C1-C5 straight or branched cha

Benzofuran compounds intermediates, and preparation method and application thereof

-

, (2016/12/01)

The invention provides a kind of benzofuran compounds intermediates, and a preparation method and application thereof, and the structure of the intermediates is shown as a general formula (I) in the specification. In the general formula (I), R1 and R3 are

Novel PdII-mediated cascade carboxylative annulation to construct benzo[b]furan-3-carboxylic acids

Liao, Yun,Smith, Jennifer,Fathi, Reza,Yang, Zhen

, p. 2707 - 2709 (2007/10/03)

(Chemical Equation Presented) Benzo[b]furan-3-carboxylic acid (2) was generated from 1 by forming three new bonds in one step via a Pd II-mediated cascade carboxylative annulation. The proposed mechanism was supported by the observation of an u

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