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Cyclohexanamine, 2-propyl-cis-, also known as cis-2-propylcyclohexanamine, is an organic compound with the molecular formula C9H19N. It is a cyclic amine derivative, where a cyclohexane ring is substituted with a propyl group and an amino group. The cis-isomer indicates that the propyl and amino groups are positioned on the same side of the cyclohexane ring. Cyclohexanamine, 2-propyl-, cis- is a colorless liquid with a characteristic amine-like odor and is used in the synthesis of various chemicals, pharmaceuticals, and agrochemicals. It is also known for its potential applications in the production of insecticides and other bioactive compounds.

2163-18-0

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2163-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2163-18-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2163-18:
(6*2)+(5*1)+(4*6)+(3*3)+(2*1)+(1*8)=60
60 % 10 = 0
So 2163-18-0 is a valid CAS Registry Number.

2163-18-0Relevant academic research and scientific papers

Novel selective inhibitors of neutral endopeptidase for the treatment of female sexual arousal disorder. Synthesis and activity of functionalized glutaramides

Pryde, David C.,Maw, Graham N.,Planken, Simon,Platts, Michelle Y.,Sanderson, Vivienne,Corless, Martin,Stobie, Alan,Barber, Christopher G.,Russell, Rachel,Foster, Laura,Barker, Laura,Wayman, Christopher,Van Der Graaf, Piet,Stacey, Peter,Morren, Debbie,Kohl, Christopher,Beaumont, Kevin,Coggon, Sara,Tute, Michael

, p. 4409 - 4424 (2007/10/03)

Female sexual arousal disorder (FSAD) is a highly prevalent sexual disorder affecting up to 40% of women. We describe herein our efforts to identify a selective neutral endopeptidase (NEP) inhibitor as a potential treatment for FSAD. The rationale for this approach, together with a description of the medicinal chemistry strategy, lead compounds, and SAR investigations are detailed. In particular, the strategy of starting with the clinically precedented selective NEP inhibitor, Candoxatrilat, and targeting low molecular weight and relatively polar mono-carboxylic acids is described. This led ultimately to the prototype development candidate R-13, for which detailed pharmacology and pharmacokinetic parameters are presented.

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