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2-morpholin-4-yl-N-(4-p-tolyl-thiazol-2-yl)-acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93023-72-4

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93023-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93023-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,0,2 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93023-72:
(7*9)+(6*3)+(5*0)+(4*2)+(3*3)+(2*7)+(1*2)=114
114 % 10 = 4
So 93023-72-4 is a valid CAS Registry Number.

93023-72-4Downstream Products

93023-72-4Relevant academic research and scientific papers

[...] aromatic amines acetylcholine esterase inhibitor synthesis and use (by machine translation)

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Paragraph 0093; 0096; 0097, (2018/10/19)

The present invention provides a formula for the (I) or (II) [...] aromatic amines of the acetylcholine esterase inhibitor and its pharmaceutically acceptable salt or a stereoisomer thereof, a process for their preparation and its in the preparation of acetylcholine esterase inhibitors and treatment of Alzheimer's disease and/or myasthenic application of the medicament, type definition of each group in the specification. The invention of aromatic amine derivatives as [...] of acetylcholine esterase inhibitors with micromolar level to nanomolar inhibiting activity, has further developed into an anti-Alzheimer's disease possibility of drug. (by machine translation)

Substituted thiazoles VII. Synthesis and antitumor activity of certain 2-(substituted amino)-4-phenyl-1,3-thiazole analogs

Hassan, Ghada S.,El-Messery, Shahenda M.,Al-Omary, Fatmah A.M.,El-Subbagh, Hussein I.

supporting information, p. 6318 - 6323 (2012/11/07)

A novel series of 2-acetamido- or 2-propanamido-4-(4-substituted phenyl)-1,3-thiazoles (11-34) was designed and synthesized. Compounds were subjected to National Cancer Institute (NCI) in vitro assessment for their antitumor activity, at a single dose of 10 μM. Most of the investigated compounds exhibited broad-spectrum antitumor activity. Compounds 19 and 28 believed to be the most active members in this study, with MG-MID GI 50, TGI, and LC50 values of 2.8, 11.4, 44.7; and 3.3, 13.1, 46.8, respectively. Compounds 19 and 28 proved to be nine and sevenfold more active than the standard antitumor drug 5-FU, respectively.

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