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N',N''-1H-isoindole-1,3-diylidenedibenzohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1107692-92-1

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1107692-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1107692-92-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,7,6,9 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1107692-92:
(9*1)+(8*1)+(7*0)+(6*7)+(5*6)+(4*9)+(3*2)+(2*9)+(1*2)=151
151 % 10 = 1
So 1107692-92-1 is a valid CAS Registry Number.

1107692-92-1Downstream Products

1107692-92-1Relevant academic research and scientific papers

Bishydrazide derivatives of isoindoline as simple anion receptors

Dydio, Pawel,Zielinski, Tomasz,Jurczak, Janusz

, p. 1525 - 1530 (2009)

Isoindoline has been investigated as a scaffold for the construction of anion receptors. A family of bishydrazide derivatives of isoindoline has been synthesized, and the anion-binding properties of these receptors were investigated both in solution and in the solid state. Enhanced affinity toward halides has been observed for isoindoline-based ligands compared to analogous pyrroledicarboxyamides. However, in the case of highly basic anions, the anion binding is accompanied by partial deprotonation of the receptors, which also leads to the color changes of ligands' solutions.

Efficient preparation of N′,N″-1H-isoindole-1,3-diylidenedicarbohydrazides via 1,1,3-trichloro-1H-isoindole, and their characterization

Hordiyenko, Olga V.,Rudenko, Igor V.,Biitseva, Angelina V.,Turov, Aleksandr V.,Arrault, Axelle,Brosse, Nicolas,Fabre, Olivier,Jamart-Grégoire, Brigitte,Zubatyuk, Roman I.,Shishkin, Oleg V.

experimental part, p. 6218 - 6225 (2011/03/20)

N′,N″-1H-Isoindole-1,3-diylidenedialkyl(aryl,heteroaryl)carbohydrazides were prepared in good yields via 1,1,3-trichloro-1H-isoindole, which was shown to be a versatile reagent for their synthesis. Tautomeric structure and conformational behaviour of dica

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