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Thiourea, N-cyclohexyl-N'-(6-methyl-2-pyridinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

140934-79-8

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140934-79-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140934-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,9,3 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 140934-79:
(8*1)+(7*4)+(6*0)+(5*9)+(4*3)+(3*4)+(2*7)+(1*9)=128
128 % 10 = 8
So 140934-79-8 is a valid CAS Registry Number.

140934-79-8Downstream Products

140934-79-8Relevant academic research and scientific papers

Synthesis and antimicrobial activity of pyridines bearing thiazoline and thiazolidinone moieties

Hassan, Hoda Y.,El-Koussi, Nawal A.,Farghaly, Zeinab S.

, p. 863 - 866 (1998)

Two series of new pyridines bearing thiazoline (3a - n) and thiazolidinone (5a - e) moieties were prepared via the cyclization of the corresponding substituted pyridyl thiourea (2a - g) with an appropriately substituted phenacyl bromide or chloroacetic ac

Diversity-Oriented Synthesis of Thiazolidine-2-imines via Microwave-Assisted One-Pot, Telescopic Approach and Its Interaction with Biomacromolecules

Saikia, Ananya Anubhav,Rao, Ramdas Nishanth,Maiti, Barnali,Balamurali, Musuvathi Motilal,Chanda, Kaushik

, p. 630 - 640 (2020/12/15)

In this work, a one-pot, telescopic approach is described for the combinatorial library of thiazolidine-2-imines. The synthetic manipulation proceeds smoothly via the reaction of 2-aminopyridine/pyrazine/pyrimidine with substituted isothiocyanates followed by base catalyzed ring closure with 1,2-dibromoethane to obtain thiazolidine-2-imines with broad substrate scope and high functional group tolerance. The synthetic strategy merges well with the thiourea formation followed by base catalyzed ring closure reaction for the thiazolidine-2-imine synthesis in a more modular and straightforward approach. The synthetic procedure reported herein represents a cleaner route toward thiazolidine-2-imines as compared to traditional methodologies. Moreover, the biological significance of combinatorially synthesized thiazolidin-2-imines has been investigated for their use as possible inhibitors for acetyl cholinesterase through molecular docking studies.

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