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1-benzyl-2-methyl-4-methylthio-2,3-dihydro-1H-1,5-benzodiazepine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

216432-71-2

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216432-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 216432-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,6,4,3 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 216432-71:
(8*2)+(7*1)+(6*6)+(5*4)+(4*3)+(3*2)+(2*7)+(1*1)=112
112 % 10 = 2
So 216432-71-2 is a valid CAS Registry Number.

216432-71-2Relevant academic research and scientific papers

Synthesis and mild conversion of 1,5-benzodiazepine iminothioethers into hydrazides

Puod?iünaité,Kosychova,Jan?iené,Stumbrevi?iüté

, p. 334 - 338 (1998)

4-Methylthio-2,3-dihydro-1H-1,5-benzodiazepine derivatives were prepared by alkylation of tetrahydro-1H-1,5-benzodiazepine-2-thiones with iodomethane or dimethyl sulfate in the presence of base or using phase-transfer catalysis. The desired 4-acyl-hydrazino-2,3-dihydro-1H-1,5-benzodiazepines resulted from the reaction of iminothioethers with hydrazides. 1998 Plenum Publishing Corporation.

New 1-(3-nitrophenyl)-5,6-dihydro-4H-[1,2,4]triazolo[4,3-a][1,5]benzodiazepines: Synthesis and computational study

Kosychova, Lidija,Karalius, Antanas,Staniulyte, Zita,Sirutkaitis, Romualdas Aleksas,Palaima, Algirdas,Laurynenas, Audrius,Anusevi?ius, ?ilvinas

, p. 5392 - 5408 (2015/05/12)

Triazole derivatives constitute an important group of heterocyclic compounds have have been the subject of extensive study in the recent past. These compounds have shown a wide range of biological and pharmacological activities. In this work, new fused tricyclic 1-(3-nitrophenyl)-5,6-dihydro-4H-[1,2,4]triazolo[4,3-a][1,5]-benzodiazepines have been synthesized by the thermal cyclization of N′-(2,3-dihydro-1H-1,5-benzodiazepin-4-yl)-3-nitrobenzohydrazides. After screening ethanol, toluene and 1-butanol as solvents, butanol-1 was found to be the best choice for the cyclization reaction in order to obtain the highest yields of tricyclic derivatives. The chemical structures of the synthesized compounds were elucidated by the analysis of their IR, 1H- and 13C-NMR spectral data. For tentative rationalization of the reaction processes, the global and local reactivity indices of certain compounds, taking part in the reaction pathway, were assessed by means of quantum mechanical calculations using the conceptual density functional theory (DFT) approach. This work could be useful for the synthesis of new heterocyclic compounds bearing a fused triazole ring.

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