219921-93-4 Usage
Description
(R)-3-methyl-1-(2-(1-pieridinyl)phenyl)-butylamine is a chiral amine compound characterized by its molecular formula C18H25N. It features a butylamine chain attached to a phenyl group, which in turn contains a pyridine ring. The (R) enantiomer of this compound is the active form, distinguishing it from its (S) counterpart. (R)-3-methyl-1-(2-(1-pieridinyl)phenyl)-butylamine is primarily utilized in the synthesis of pharmaceuticals and other organic compounds, with potential implications in drug development and research due to its possible biological activity.
Uses
Used in Pharmaceutical Synthesis:
(R)-3-methyl-1-(2-(1-pieridinyl)phenyl)-butylamine is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and chirality make it a valuable building block for creating novel drugs with specific therapeutic properties.
Used in Drug Development and Research:
In the field of drug development and research, (R)-3-methyl-1-(2-(1-pieridinyl)phenyl)-butylamine serves as a promising candidate for the discovery of new therapeutic agents. Its potential biological activity and structural features can be exploited to design and develop innovative drugs targeting specific medical conditions.
Used in Organic Chemistry:
(R)-3-methyl-1-(2-(1-pieridinyl)phenyl)-butylamine is also employed in organic chemistry as a versatile reagent or starting material for the preparation of a wide range of organic compounds. Its amine and phenyl functionalities can be further modified or functionalized to synthesize complex organic molecules with diverse applications.
Used in Chiral Compounds Research:
The chirality of (R)-3-methyl-1-(2-(1-pieridinyl)phenyl)-butylamine makes it an interesting subject for research in the field of chiral compounds. Understanding the properties and applications of chiral molecules is crucial for various scientific and industrial applications, including the development of enantiomerically pure drugs with improved efficacy and reduced side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 219921-93-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,9,2 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 219921-93:
(8*2)+(7*1)+(6*9)+(5*9)+(4*2)+(3*1)+(2*9)+(1*3)=154
154 % 10 = 4
So 219921-93-4 is a valid CAS Registry Number.
219921-93-4Relevant articles and documents
Reversal diastereoselectivity between the organomagnesium and organolithium reagents on Chiral N-tert-butylsulfinylaldimines for the preparation of chiral amines
Rajendiran, Chinnapillai,Nagarajan, Periyandi,Naidu,Dubey
, p. 2936 - 2942 (2014/11/08)
The asymmetric synthesis of both the enantiomer of chiral amines from the single chiral source of N-tert-butylsulfinylaldimines (3) by simply changing the organometallic reagents through diastereoselective addition. An efficient enantioselective synthesis of chiral amines including (S)-3-methyl-1-(2- piperidin-1-yl-phenyl)butyl amine (6a), a key intermediate to prepare antidiabetic drug repaglinide (1), is reported.
Process for the preparation of substantially optically pure Repaglinide and precursors thereof
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Page/Page column 13, (2010/05/13)
The invention relates to a process for preparing substantially optically pure Repaglinide and pharmaceutically acceptable salts, solvates and esters thereof, as well as precursors therefore.
