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2-Propanol, 1-[(1-methylethyl)amino]-3-(3-methylphenoxy)-, (2R)- is a complex organic compound with the chemical formula C12H19NO. It is a chiral molecule, meaning it has a non-superimposable mirror image, and the (2R)- notation indicates the specific configuration of the molecule. 2-Propanol, 1-[(1-methylethyl)amino]-3-(3-methylphenoxy)-, (2R)- is characterized by a 2-propanol backbone, with an amino group attached to the 1st carbon, a 3-methylphenoxy group at the 3rd carbon, and an isopropyl (1-methylethyl) group on the nitrogen. It is a colorless liquid with a specific optical rotation, indicating its chiral nature. 2-Propanol, 1-[(1-methylethyl)amino]-3-(3-methylphenoxy)-, (2R)- is used in various applications, including as a pharmaceutical intermediate and in the synthesis of other organic compounds. Its chemical structure and properties make it a versatile building block in organic chemistry, particularly in the development of chiral molecules with specific biological activities.

4198-88-3

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4198-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4198-88-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,9 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4198-88:
(6*4)+(5*1)+(4*9)+(3*8)+(2*8)+(1*8)=113
113 % 10 = 3
So 4198-88-3 is a valid CAS Registry Number.

4198-88-3Upstream product

4198-88-3Downstream Products

4198-88-3Relevant academic research and scientific papers

Effect of basic and acidic additives on the separation of some basic drug enantiomers on polysaccharide-based chiral columns with acetonitrile as mobile phase

Gogaladze, Khatuna,Chankvetadze, Lali,Tsintsadze, Maia,Farkas, Tivadar,Chankvetadze, Bezhan

, p. 228 - 234 (2015)

The separation of enantiomers of 16 basic drugs was studied using polysaccharide-based chiral selectors and acetonitrile as mobile phase with emphasis on the role of basic and acidic additives on the separation and elution order of enantiomers. Out of the studied chiral selectors, amylose phenylcarbamate-based ones more often showed a chiral recognition ability compared to cellulose phenylcarbamate derivatives. An interesting effect was observed with formic acid as additive on enantiomer resolution and enantiomer elution order for some basic drugs. Thus, for instance, the enantioseparation of several β-blockers (atenolol, sotalol, toliprolol) improved not only by the addition of a more conventional basic additive to the mobile phase, but also by the addition of an acidic additive. Moreover, an opposite elution order of enantiomers was observed depending on the nature of the additive (basic or acidic) in the mobile phase.

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