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41097-47-6

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41097-47-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41097-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,9 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41097-47:
(7*4)+(6*1)+(5*0)+(4*9)+(3*7)+(2*4)+(1*7)=106
106 % 10 = 6
So 41097-47-6 is a valid CAS Registry Number.

41097-47-6Relevant articles and documents

Ruthenium(ii)-catalysed 1,2-selective hydroboration of aldazines

Gunanathan, Chidambaram,Pradhan, Subham,Thiyagarajan, Subramanian

supporting information, p. 7147 - 7151 (2021/08/30)

Herein, an efficient and simple catalytic method for the selective and partial reduction of aldazines using ruthenium catalyst [Ru(p-cymene)Cl2]2 (1) has been accomplished. Under mild conditions, aldazines undergo the addition of pinacolborane in the presence of a ruthenium catalyst, which delivered N-boryl-N-benzyl hydrazone products. Notably, the reaction is highly selective, and results in exclusive mono-hydroboration and desymmetrization of symmetrical aldazines. Mechanistic studies indicate the involvement of in situ formed intermediate [{(η6-p-cymene)RuCl}2(μ-H-μ-Cl)] (1a) in this selective hydroboration.

Synthesis and antimicrobial activity of some new coumarin and dicoumarol derivatives

El-Metwally, Souad A.,Regal, Mohsen K. A.,Shaban, Safa S.

, (2020/01/22)

PTC reaction of coumarin derivative 1 with alkyl halides afforded C4 oxygen alkylation products 2a-d in appreciative yield, whereas with phenyl isothiocyanate gives the C3 addition product 4; also, one-pot three-component PTC reactio

Dihydrazone compound high in affinity with Abeta protein and Tau protein, derivative thereof, and applications of dihydrazone compound and derivative

-

Paragraph 0029-0031; 0047-0049, (2019/05/15)

The invention provides a dihydrazone compound high in affinity with Abeta protein and Tau protein, a derivative thereof, and applications of the dihydrazone compound and the derivative. The structureof the dihydrazone compound is represented by formula I. The dihydrazone compound can be directly taken as a fluorescence probe used for detecting neurofibrillary tangles in vivo or in tissue samples;when the dihydrazone compound is adopted in nuclear medicine imaging, appropriate radioisotopes are needed for labeling. The dihydrazone compound is especially suitable to be used for diagnosis of neurodegenerative diseases, and diagnosis of patients with diseases with Abeta plaques including Alzheimer's disease.

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