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N-{4-[phenyldiazenyl]phenyl}hydrazinecarbothioamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

864724-63-0

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864724-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 864724-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,7,2 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 864724-63:
(8*8)+(7*6)+(6*4)+(5*7)+(4*2)+(3*4)+(2*6)+(1*3)=200
200 % 10 = 0
So 864724-63-0 is a valid CAS Registry Number.

864724-63-0Downstream Products

864724-63-0Relevant academic research and scientific papers

Synthesis and anticonvulsant and neurotoxicity evaluation of N 4-phthalimido phenyl (thio) semicarbazides

Yogeeswari,Sriram,Saraswat,Ragavendran, J. Vaigunda,Kumar, M. Mohan,Murugesan,Thirumurugan,Stables

, p. 341 - 346 (2003)

The phenyl (thio) semicarbazide derivatives of phthalimido pharmacophore were synthesized and evaluated for their anticonvulsant and neurotoxic properties. Initial anticonvulsant screening was performed using intraperitoneal (i.p.), maximal electroshock-induced seizure (MES), subcutaneous pentylenetetrazole (scPTZ) and subcutaneous strychnine (sc STY)-induced seizure threshold tests in mice. Compound 2c afforded protection in all the three screens. Compounds except 1d, 2a and 2d showed no neurotoxicity up to 300mg/kg. Compounds 1a, 1b, 2c, 2d, 2g and 2i were found to show oral MES activity. The compounds exhibited CNS depression and behavioral despair side effects, lesser than the conventional antiepileptic drugs.

Some nucleophilic reactions with isothiocyanatoazobenzene

El-Adasy, Abu-Bakr A. A. M.

, p. 2625 - 2635 (2008/03/11)

The reactivity of Isothiocyanatoazobenzene 2 towards some nucleophiles was investigated. Thus, reaction of isothiocyanate 2 with aromatic amines gave thioureas 3a-d. The reaction of compound 3a with arylidenemalononitriles 4a,b afforded the corresponding

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