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N-(5-phenylpentyl)-1,2-ethanediamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

785774-71-2

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785774-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 785774-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,5,7,7 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 785774-71:
(8*7)+(7*8)+(6*5)+(5*7)+(4*7)+(3*4)+(2*7)+(1*1)=232
232 % 10 = 2
So 785774-71-2 is a valid CAS Registry Number.

785774-71-2Downstream Products

785774-71-2Relevant academic research and scientific papers

Synthesis of 6- to 10-membered ring (E)- hydroxyiminohydroazaazoniabenzocycloalkenes derivative from cyclization of 2-nitromethylene-1-(ω-phenylalkyl)imidazolidine or 2-nitromethylene-1- (ω-phenylalkyl)hexahydropyrimidine in trifluoromethanesulfonic acid

Coustard, Jean-Marie,Soro, Yaya,Siaka, Sorho,Bamba, Fanté,Cousson, Alain

, p. 3320 - 3328 (2007/10/03)

In trifluoromethanesulfonic acid, 2-nitromethylene-1-(ω-phenylalkyl) imidazolidine or 2-nitromethylene-1-(ω-phenylalkyl)hexahydropyrimidine derivatives undergo an intramolecular cyclization to afford (E)- hydroxyiminohydroazaazoniabenzocycloalkenes, in th

Preparation of ternary platinum(II) complexes with N-(ω-phenylalkyl)- 1,2-ethanediamine and 2,2′-dipyridine and the effect of the methylene chain length of the N-(ω-phenylalkyl)-1,2-ethanediamine in the complexes on intermolecular interactions with various arylsulfonates

Goto, Masafumi,Tanaka, Katsutoshi,Sumimoto, Masamitsu,Mori, Hiromasa,Kurosaki, Hiromasa

, p. 649 - 653 (2007/10/03)

A series of ternary complexes comprised of platinum(II), 2,2′-dipyridine, and N-(ω-phenylalkyl)-1,2-ethanediamine was prepared by varying the number (n) of methylene chain carbons between the phenyl group and one of the amino groups of 1,2-ethanediamine. NMR measurements indicated that intramolecular stacking occurred for n=1 and intermolecular stacking occurred for n=3 for several of the aryl sulfonates.

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