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17531-59-8

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17531-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17531-59-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,3 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17531-59:
(7*1)+(6*7)+(5*5)+(4*3)+(3*1)+(2*5)+(1*9)=108
108 % 10 = 8
So 17531-59-8 is a valid CAS Registry Number.

17531-59-8Relevant articles and documents

Synthesis, characterization and physiochemical information, along with antimicrobial studies of some metal complexes derived from an ON donor semicarbazone ligand

Siji,Kumar, M.R. Sudarsana,Suma,Kurup, M.R. Prathapachandra

, p. 22 - 28 (2010)

Eight new transition metal complexes of benzaldehyde-N(4)-phenylsemicarbazone have been synthesized and characterized by elemental analyses, molar conductance, electronic and infrared spectral studies. In all the complexes, the semicarbazone is coordinate

Microwave-assisted Synthesis and Bioevaluation of Some Semicarbazones

Jafri, Laila,Ansari, Farzana L.,Jamil, Maryam,Kalsoom, Saima,Qureishi, Sana,Mirza, Bushra

experimental part, p. 950 - 959 (2012/08/28)

In continuation to our efforts in finding potential therapeutic agents, a variety of biologically significant semicarbazones were synthesized by the reaction of different carbonyl compounds with phenyl semicarbazides through microwave irradiation. Initial

Structural modifications of the primary amino group of anticonvulsant aryl semicarbazones

Dimmock,Puthucode,Lo,Quail,Yang,Stables

, p. 83 - 88 (2007/10/02)

A number of aryl semicarbazones had been shown previously to possess significant anticonvulsant properties. The principal objective of the present investigation was to determine the importance of the primary amino group in this series of compounds by replacing it with other substituents. The results indicate that the amino group was not essential for anticonvulsant activity. However its replacement by an aryl ring generally abolished activity while a terminal phenylamino function was better tolerated. Thus both the size of the group and its hydrogen bonding capabilities appear to influence bioactivity. Alteration of the oxygen atom of the semicarbazones by isosteres did not enhance anticonvulsant properties.

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