89985-60-4 Usage
Uses
Used in Organic Synthesis:
3-Buten-1-ol, 2-amino-, (2R)is used as a building block in organic synthesis for the creation of various compounds. Its unique structure with both an amino and hydroxyl group allows for versatile reactions and the formation of a wide range of products.
Used in Pharmaceutical Research:
In pharmaceutical research, 3-Buten-1-ol, 2-amino-, (2R)serves as a key intermediate in the synthesis of pharmaceuticals. Its properties make it a valuable component in the development of new drugs and medicinal compounds.
Used in Stereochemical Studies:
The (2R)-enantiomer of 3-Buten-1-ol, 2-aminois important in stereochemical studies, where the spatial arrangement of atoms is crucial for biological activity. It aids in understanding the role of chirality in chemical reactions and biological systems.
Used in the Development of Chiral Catalysts and Ligands:
3-Buten-1-ol, 2-amino-, (2R)is utilized in the development of chiral catalysts and ligands for asymmetric synthesis. Its enantioselective properties are essential for creating compounds with specific three-dimensional structures, which is vital in many chemical and pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 89985-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,8 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89985-60:
(7*8)+(6*9)+(5*9)+(4*8)+(3*5)+(2*6)+(1*0)=214
214 % 10 = 4
So 89985-60-4 is a valid CAS Registry Number.
89985-60-4Relevant academic research and scientific papers
C10-ALKYLENE SUBSTITUTED 13-MEMBERED MACROLIDES AND USES THEREOF
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Paragraph 00617, (2020/06/10)
Provided are 13-membered macrolides for the treatment of infectious diseases. The 13-membered macrolides described herein are azaketolides. Also provided are methods for preparing the 13- membered macrolides, pharmaceutical compositions comprising the 13-membered macrolides, and methods of treating infectious diseases, and in particular, disease resulting from Gram negative bacteria using the disclosed macrolides. Formula (I)
An oligomer-based approach to skeletal diversity in small-molecule synthesis
Spiegel, David A.,Schroeder, Frank C.,Duvall, Jeremy R.,Schreiber, Stuart L.
, p. 14766 - 14767 (2008/02/09)
Access to small molecules of widely varying molecular shapes has been identified as an enabling step in the discovery of biologically active materials. In this communication we introduce an approach to the systematic development of architecturally distinc
Synthesis of enantiomerically pure (+)- and (-)-protected 5-aminomethyl-1,3-oxazolidin-2-one derivatives from allylamine and carbon dioxide
Fernandez, Isabelle,Munoz, Luis
, p. 2548 - 2557 (2007/10/03)
The stereoselective synthesis of enantiomerically pure (5R)- and (5S)-aminomethyl-oxazolidinones with different protecting groups have been carried out from an allyl amine as the source of the carbon backbone. The key reaction is the high yield iodiocyclization of enantiomerically pure allylphenethyl amine in the presence of carbon dioxide.
