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Benzeneacetic acid, a-methyl-4-(2-methylpropyl)-, 2-[(phenylamino)thioxomethyl]hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127222-71-3

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127222-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127222-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,2,2 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 127222-71:
(8*1)+(7*2)+(6*7)+(5*2)+(4*2)+(3*2)+(2*7)+(1*1)=103
103 % 10 = 3
So 127222-71-3 is a valid CAS Registry Number.

127222-71-3Relevant academic research and scientific papers

Design and Synthesis of Novel Ibuprofen Derivatives as Selective COX-2 Inhibitors and Potential Anti-Inflammatory Agents: Evaluation of PGE2, TNF-α, IL-6 and Histopathological Study

El-Dash, Yara Sayed,El-Nassan, Hala Bakr,Halim, Peter Amir

, p. 427 - 443 (2022/03/09)

Background: The reported binding mode of ibuprofen in the COX-2 binding site indicat-ed that the carboxylic group binds with Arg-120 and Tyr-355 at the entrance of the cyclooxygenase channel and does not extend into the pocket. This accounted for the non-

Biology-oriented drug synthesis (BIODS), in vitro urease inhibitory activity, and in silico studies on ibuprofen derivatives

Seraj, Faiza,Kanwal,Khan, Khalid Mohammed,Khan, Ajmal,Ali, Muhammad,Khalil, Ruqaiya,Ul-Haq, Zaheer,Hameed, Shehryar,Taha, Muhammad,Salar, Uzma,Perveen, Shahnaz

, p. 143 - 157 (2020/01/28)

Abstract: Novel ibuprofen derivatives 1–19 including ibuprofen hydrazide 1, and substituted thiourea derivatives 2–19 were synthesized and characterized by EI-MS, FAB-MS, HREI-MS, HRFAB-MS, 1H-, and 13C-NMR spectroscopic techniques.

Design, synthesis and antiinflammatory activity of some 1,3,4-oxadiazole derivatives

Omar,Mahfouz,Rahman

, p. 819 - 825 (2007/10/03)

A series of substituted 1,3,4-oxadiazole derivatives 19-34 were synthesized as antiinflammatory agents. The target compounds were obtained by cyclodesulfurization of the corresponding thiosemicarbazides 3-18 using either dicyclohexylcarbodiimide DCC, or I

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