1171183-40-6 Usage
Description
(R)-methyl 2-(benzyloxycarbonyl)-5-cyanopentanoate, with the molecular formula C15H17NO4, is a chemical compound that serves as a highly versatile reagent in organic synthesis and chemical research. It is known for its ability to act as a building block in numerous chemical reactions, making it a valuable asset in the preparation of complex organic molecules.
Uses
Used in Organic Synthesis:
(R)-methyl 2-(benzyloxycarbonyl)-5-cyanopentanoate is used as a versatile building block for the synthesis of complex organic molecules, due to its ability to participate in various chemical reactions.
Used in Pharmaceutical Synthesis:
(R)-methyl 2-(benzyloxycarbonyl)-5-cyanopentanoate is used as a precursor in the synthesis of various pharmaceuticals and bioactive compounds, contributing to the development of new drugs and therapies.
Used as a Chiral Auxiliary:
(R)-methyl 2-(benzyloxycarbonyl)-5-cyanopentanoate is also utilized as a chiral auxiliary, enabling the selective synthesis of enantiomerically pure compounds, which is crucial for the production of specific pharmaceuticals and organic molecules with desired properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1171183-40-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,1,1,8 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1171183-40:
(9*1)+(8*1)+(7*7)+(6*1)+(5*1)+(4*8)+(3*3)+(2*4)+(1*0)=126
126 % 10 = 6
So 1171183-40-6 is a valid CAS Registry Number.
1171183-40-6Relevant articles and documents
IBX/TBAB-mediated oxidation of primary amines to nitriles
Drouet, Fleur,Fontaine, Patrice,Masson, Geraldine,Zhu, Jieping
, p. 1370 - 1374 (2009)
The combination of o-iodoxybenzoic acid (IBX) and tetrabutylammonium bromide (TBAB) efficiently oxidizes primary amines to the corresponding nitriles in good to excellent yield under mild conditions. The reaction is racemization-free when applied to a chiral lysine derivative. Georg Thieme Verlag Stuttgart.
