159878-02-1 Usage
Description
Benzyl (1R,2S)-3-chloro-2-hydroxy-1-(phenylthiomethyl)propylcarbamate is a complex organic compound characterized by its unique molecular structure. It is a white solid with specific stereochemistry, which is crucial for its potential applications and interactions with other molecules.
Uses
Used in Organic Synthesis:
Benzyl (1R,2S)-3-chloro-2-hydroxy-1-(phenylthiomethyl)propylcarbamate is used as an intermediate in organic synthesis for the development of various pharmaceuticals and chemical compounds. Its unique structure and functional groups make it a valuable building block for creating new molecules with specific properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Benzyl (1R,2S)-3-chloro-2-hydroxy-1-(phenylthiomethyl)propylcarbamate is used as a key component in the synthesis of drugs targeting specific medical conditions. Its chemical properties allow for the creation of molecules with potential therapeutic effects, contributing to the development of novel treatments.
Used in Chemical Research:
Benzyl (1R,2S)-3-chloro-2-hydroxy-1-(phenylthiomethyl)propylcarbamate is also utilized in chemical research to study the properties and behavior of complex organic molecules. Its unique structure provides insights into the interactions between different molecular components and can lead to a better understanding of chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 159878-02-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,8,7 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 159878-02:
(8*1)+(7*5)+(6*9)+(5*8)+(4*7)+(3*8)+(2*0)+(1*2)=191
191 % 10 = 1
So 159878-02-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H20ClNO3S/c19-11-17(21)16(13-24-15-9-5-2-6-10-15)20-18(22)23-12-14-7-3-1-4-8-14/h1-10,16-17,21H,11-13H2,(H,20,22)/t16-,17+/m0/s1
159878-02-1Relevant articles and documents
Merging lithium carbenoid homologation and enzymatic reduction: A combinative approach to the HIV-protease inhibitor Nelfinavir
Castoldi, Laura,Ielo, Laura,Hoyos, Pilar,Hernáiz, María J.,De Luca, Laura,Alcántara, Andrés R.,Holzer, Wolfgang,Pace, Vittorio
, p. 2211 - 2217 (2018/03/28)
An effective stereocontrolled synthesis of the HIV protease inhibitor Nelfinavir is reported. Two transformations were identified crucial for achieving success: the formation of a densely functionalized α-chloroketone via the homologation of a Weinreb ami
Development of a continuous process for the industrial generation of diazomethane
Proctor, Lee D.,Warr, Antony J.
, p. 884 - 892 (2013/09/06)
The development of a safe process for the industrial generation of diazomethane is described. Diazomethane is produced and consumed in a continuous process capable of generating between 50 and 60 tonnes per year whilst the maximum inventory is maintained
Process for reducing α-amino ketones
-
, (2008/06/13)
The present invention has its objects to provide a method for reducing α-aminoketone derivatives under mild conditions with high stereoselectivity. This invention is a method for reducing α-aminoketone which comprises reacting an a-aminoketone derivative of general formula (1) with a compound prepared from an organoaluminum compound of general formula (4), a sulfonic acid derivative of general formula (5), and an alcohol compound of general formula (6) to give an α-aminoalcohol derivative of general formula (7)