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N-(2-methylphenyl)-N'-(2-pyridinyl)urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13143-26-5

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13143-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13143-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,4 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13143-26:
(7*1)+(6*3)+(5*1)+(4*4)+(3*3)+(2*2)+(1*6)=65
65 % 10 = 5
So 13143-26-5 is a valid CAS Registry Number.

13143-26-5Downstream Products

13143-26-5Relevant academic research and scientific papers

USE OF DDX3X INHIBITORS FOR THE TREATMENT OF PNEUMOVIRUS INFECTIONS

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Page/Page column 30; 33; 34, (2015/10/05)

The invention relates to a DDX3X inhibitorfor use in the treatment of pneumovirus infection in a mammal, wherein the DDX3X inhibitor may be a compound of Formula (I) wherein y, Z, R1, X, L, Ra and Rb are as defined herein.

Synthesis of unsymmetrical 2-pyridyl ureas via selenium-catalyzed oxidative carbonylation of 2-aminopyridine with aromatic amines

Zhang, Xiaopeng,Li, Desheng,Ma, Xueji,Wang, Yan,Zhang, Guisheng

, p. 1357 - 1363 (2013/07/05)

A simple, one-pot, phosgene-free approach to a series of unsymmetrical 2-pyridyl ureas starting from 2-aminopyridine and various aromatic amines is reported for the first time. The procedure employs inexpensive selenium as the catalyst, and carbon monoxide (instead of phosgene) as the carbonyl reagent. The products are obtained in moderate to good yields via selenium-catalyzed oxidative cross-carbonylation of the substrate amines in the presence of oxygen. The selenium functions as a phase-transfer catalyst and can be recovered easily and reused without any significant degradation of its catalytic activity.

Heteroacyl Azides as Acylating Agents for Aromatic or Heteroatomic Amines (1)

Stanovnik, B.,Tisler, M.,Golob, V.,Hvala, I.,Nikolic, O.

, p. 733 - 736 (2007/10/02)

The possibility of formation of substituted heterocyclic amides from heteroacyl azides and aromatic or heteroatomic amines was investigated.Although acylation proceeded in some cases under mild reaction conditions, formation of N,N'-disubstituted ureas was the main process at elevated temperatures.

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