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74451-57-3

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74451-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74451-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,5 and 1 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 74451-57:
(7*7)+(6*4)+(5*4)+(4*5)+(3*1)+(2*5)+(1*7)=133
133 % 10 = 3
So 74451-57-3 is a valid CAS Registry Number.

74451-57-3Relevant articles and documents

A versatile synthesis, PM3-semiempirical, antibacterial, and antitumor evaluation of some bioactive pyrazoles

Hamama, Wafaa S.,El-Gohary, Hamada G.,Soliman, Mamdouh,Zoorob, Hanfi H.

experimental part, p. 543 - 554 (2012/08/27)

This research work describes the synthesis and biological properties of some novel isolated or fused heterocyclic ring systems with pyrazole, for example; enaminones containing pyrazolone ring photochromic functional unit, 4-[(4-chlorophenylamino)methylene]-3-methyl-1-phenyl-1H-pyrazol-5(4H)-one (3) and some analogous derivatives 4, 9, and 10, also as pyrazolo[3,4-b]pyridine, pyrazolo[3,4-b]quinoline, pyrazolo[3',4':4,5]thieno[2,3-c]pyrazoline and pyrazolo[3,4-c]pyrazole were synthesized and characterized. Newly synthesized compounds were characterized by IR, 1H NMR, 13C NMR, mass spectral data and quantum mechanical calculations. Selected products were tested for their antibacterial and antitumor agents.

About the Reaction of "Pyrazolone Blue" with Diazomethane

Hennig, L.,Haessner, R.,Rissanen, K.

, p. 584 - 590 (2007/10/02)

The reaction of "pyrazolone blue" with diazomethane was investigated.A pyridazinone derivative 3, a heterocyclic spiro-cyclopropyl product 4 and a compound 7, which contains three pyrazolone and two diazomethane entities, are formed. 3 reacts with an exce

Oxopyrazoline-spiro-oxirans. A New Class of Reactive Heterocycles

Ege, Seyhan N.,Adams, Alan. D.,Gess, E. Joseph,Ragone, Katherine S.,Kober, Brian J.,et al.

, p. 325 - 332 (2007/10/02)

Chemical and spectral properties of a series of 1-oxa-5,6-diazaspirohept-6-en-4-ones, synthesized by the oxidation of 4-alkylidene- or 4-arylidene-1-aryl-2-pyrazolin-5-ones are reported

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