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1-[(isopropylamino)(phenyl)methyl]cyclopentanol is a complex organic compound with the molecular formula C18H27NO. It features a cyclopentanol core, which is a cyclopentane ring with a hydroxyl group attached to one of the carbons. The molecule is further characterized by an isopropylamino group (a nitrogen atom bonded to two hydrogen atoms and an isopropyl group) and a phenyl group (a benzene ring) attached to a methylene bridge (a carbon atom with two hydrogen atoms) that connects to the cyclopentanol core. This structure gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals or chemical research.

7015-48-7

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7015-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7015-48-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,1 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7015-48:
(6*7)+(5*0)+(4*1)+(3*5)+(2*4)+(1*8)=77
77 % 10 = 7
So 7015-48-7 is a valid CAS Registry Number.

7015-48-7Downstream Products

7015-48-7Relevant academic research and scientific papers

Samarium diiodide/nickel diiodide an efficient system for homo and heterocoupling reactions of imines

Machrouhi, Fouzia,Namy, Jean-Louis

, p. 1315 - 1318 (1999)

Samarium diiodide in the presence of a catalytic amount of nickel diiodide mediates a very fast dimerization of imines into vicinal diamines and the mixed coupling of imines and ketones to give β-amino alcohols.

Direct reductive coupling of secondary amides: Chemoselective formation of vicinal diamines and vicinal amino alcohols

Huang, Pei-Qiang,Lang, Qi-Wei,Wang, Ai-E,Zheng, Jian-Feng

supporting information, p. 1096 - 1099 (2015/02/19)

We report the first one-pot reductive homocoupling reaction of secondary amides and cross-coupling reaction of secondary amides with ketones to give secondary vicinal diamines and amino alcohols. This method relies on the direct generation of α-amino carb

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