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1-phenyl-3-(thiophen-2-yl)urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75322-56-4

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75322-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75322-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,2 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 75322-56:
(7*7)+(6*5)+(5*3)+(4*2)+(3*2)+(2*5)+(1*6)=124
124 % 10 = 4
So 75322-56-4 is a valid CAS Registry Number.

75322-56-4Downstream Products

75322-56-4Relevant academic research and scientific papers

Synthetic method and application of urea compound

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Paragraph 0159-0162, (2019/06/07)

The invention relates to a synthetic method of a urea compound, comprising the following steps: adding substituted oxazolone and sodium acetate into a methanol solution, and adding substituted amine under the stirring condition, reacting and carrying out column chromatography to obtain the urea compound. The defect that dangerous compounds need to be used during existing synthetic process is overcome, and a one-pot method is adopted to replace an existing reaction with low yield. The method of the invention has mild reaction condition, the operation is simple, raw materials are easily available, and the substrate can be converted into various other useful molecules. The compound has strong practicality, and can be applied to synthesis of the pesticide daimuron, dieresis long and the anti-cancer drug Sorafenib. The invention relates to a green and environmentally-friendly unsymmetrical urea compound synthesis method with simple process and low cost.

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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