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107127-56-0

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107127-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107127-56-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,1,2 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 107127-56:
(8*1)+(7*0)+(6*7)+(5*1)+(4*2)+(3*7)+(2*5)+(1*6)=100
100 % 10 = 0
So 107127-56-0 is a valid CAS Registry Number.

107127-56-0Downstream Products

107127-56-0Relevant articles and documents

Synthesis and spectral characterization of ternary complexes of oxovanadium(IV) containing some acid hydrazones and 2,2′-bipyridine

Sreeja,Kurup, M.R. Prathapachandra

, p. 331 - 336 (2005)

An interesting series of heterocyclic base adducts of oxovanadium(IV) complexes have been synthesized by the reaction of vanadium(IV) oxide acetylacetonate with some hydrazones (H2L) in the presence of a heterocyclic base 2,2′-bipyridine. The c

Acid–Base Properties and Kinetics of Hydrolysis of Aroylhydrazones Derived from Nicotinic Acid Hydrazide

Benkovi?,Kontrec,Tomi?i?,Budimir,Gali?

, p. 1227 - 1245 (2016/08/30)

A series of aroylhydrazones were synthesized from nicotinic acid hydrazide and differently substituted benzaldehydes. The protonation constants of the 12 resulting hydrazones, as well as of the starting compounds, were determined in methanol/water 1/1 mix

Acylhydrazide schiff bases: Synthesis and antiglycation activity

Khan, Khalid Mohammed,Taha, Muhammad,Rahim, Fazal,Fakhri, Muhammad Imran,Jamil, Waqas,Khan, Momin,Rasheed, Saima,Karim, Aneela,Perveen, Shahnaz,Choudhary, Mohammad Iqbal

, p. 929 - 937 (2013/07/26)

Acylhydrazide Schiff bases 1-27 were synthesized and their in vitro antiglycation potential was evaluated. Compounds 16 (IC50 = 199.82 ± 10.6 μM), 27 (IC50 = 234.83 ± 10.28 μM), 2 (IC50 = 240.99 ± 4.2 μM), and 14 (IC50 = 276.2 ± 2.3 μM) showed antiglycation potential comparable to the standard rutin (IC50 = 294.50 ± 1.5 μM). From this study we identified a new series of potent antiglycating agents. A structure-activity relationship has been described, while all compounds were characterized by using different spectroscopic techniques.

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