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255065-87-3

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255065-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 255065-87-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,5,0,6 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 255065-87:
(8*2)+(7*5)+(6*5)+(5*0)+(4*6)+(3*5)+(2*8)+(1*7)=143
143 % 10 = 3
So 255065-87-3 is a valid CAS Registry Number.

255065-87-3Relevant articles and documents

Synthesis of imidazole derivatives: Ester and hydrazide compounds with antioxidant activity using ionic liquid as an efficient catalyst

Abdelhamid, Antar A.,Salah, Hanan A.,Marzouk, Adel A.

, p. 676 - 685 (2019/11/14)

The pyrrolidinium hydrogen sulfate (PHS) was used as an excellent ionic liquid catalyst for the preparation of many imidazoles moiety, which have biologically application via one-pot multicomponent reaction. Imidazoles were afforded through the reaction o

Microwave-assisted synthesis of 2,4,5-triphenyl-1h-imidazole containing schiff base derivatives with potential antioxidant and anticancer activities

Satyanarayana,Rakshit, Madhumita,Sivakumar

, p. 1212 - 1218 (2012/01/03)

2-(2,4,5-Triphenyl-1H-imidazol-1-yl)acetohydrazide (3) was utilized as key intermediate for the synthesis of some new Schiff bases 4a-k and 5 under reflux temperature as well as microwave irradiation. All the synthesized compounds were characterized by IR

Synthesis, characterization of some new five membered heterocycles based on imidazole moiety and their applications on therapeutics

Satyanarayana,Sivakumar,Ghosh, Asit Ranjan

, p. 276 - 283 (2013/01/10)

Different imidazole derivatives were prepared by utilizing the intermediate 2-(2,4,5-triphenyl-1H-imidazol-1- yl)acetohydrazide (3) using microwave irradiation method besides the traditional ones. They were used for synthesis of some new derivatives of 2,5-disubstituted-1,3,4-oxadiazole, pyrazole, 2,5-dimethylpyrrole and nitrogen containing five membered rings. All the synthesized compounds were characterized by IR, 1H & 13C NMR and mass spectral data. The antibacterial, antifungal (MIC) and antioxidant activities were verified for all the synthesized compounds.

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