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1-(5-(4-(dimethylamino)phenyl)-3-(thiophen-2-yl)-1H-pyrazol-1-yl)ethan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

864436-01-1

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864436-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 864436-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,4,3 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 864436-01:
(8*8)+(7*6)+(6*4)+(5*4)+(4*3)+(3*6)+(2*0)+(1*1)=181
181 % 10 = 1
So 864436-01-1 is a valid CAS Registry Number.

864436-01-1Relevant academic research and scientific papers

Design and synthesis of novel pyrazoles, pyrazolines, and pyridines from chalcone derivatives with evaluation of their in vitro anticancer activity against T-47D and UACC-257 cell lines

Mangouda, Mangoud M.,Hussein, Mohamed Z.,El-Bordany, Eman A.

, p. 5203 - 5218 (2021/01/18)

Novel series of pyrazoline carbothioamides, acetyl pyrazoles, pyridine-3-carbonitrile, pyridine-2-carbonitriles, and nicotinonitriles were synthesized. The structures of the newly synthesized compounds were established based on their spectral data, elemen

Synthesis of 3,5-disubstituted pyrazoles and their derivatives

Ingle,Doshi,Raut,Kadu

scheme or table, p. 1691 - 1698 (2012/06/15)

2-Acetylthiophene condenses with different aromatic aldehyde in ethanol in the presence of aqueous NaOH to give 1-(2′-thienyl)-3-(substituted phenyl)-2-propen-1-one (Ia-e) which reacts with hydrazine hydrate in ethanol to give pyrazoline (IIa-e) and also treated with DMSO in presence of catalytic amount of iodine to give pyrazole (II′a-e) Similarly, 1-phenyl pyrazoline (IIIa-e) treated with DMSO/I2 to give 1-phenyl pyrazole(III′a- e), 1-(2,4-dinitro phenyl) pyrazoline (IVa-e) treated with DMSO/I2 to give 1-(2,4-dinitro phenyl) pyrazole(IV′a-e), 1-carboxamido pyrazoline (Va-e) treated with DMSO/I2 to give 1-carboxamido pyrazole (V′a-e), 1-acetyl pyrazoline (VIa-e) treated with DMSO/I2 to give 1-acetyl pyrazole (VI′a-e), 1-benzoyl pyrazoline (VIIa-e) treated with DMSO/I2 to give 1-benzoyl pyrazole (VII′a-e) and 1-nitroso pyrazoline (VIIIa-e) treated with DMSO/I2 to give 1-nitroso pyrazole (VIII′a-e). Characterization and structural elucidation was carried out on the basis of melting points determination, analytical and spectral studies.

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