1312713-37-3 Usage
Description
Tert-butyl 3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate is a stable chemical molecule used as a reagent in organic synthesis. It features a piperidine ring with a carboxylate group at the 1 position and a boronate ester at the 2 position, along with a tert-butyl group attached to the nitrogen atom of the piperidine ring. Tert-butyl 3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate serves as a building block for constructing more complex organic molecules and acts as a precursor in the synthesis of pharmaceutical compounds and other biologically active molecules.
Uses
Used in Pharmaceutical Industry:
Tert-butyl 3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate is used as a precursor for the synthesis of pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, Tert-butyl 3-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate is utilized as a building block for constructing more complex organic molecules, facilitating the creation of a wide range of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 1312713-37-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,7,1 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1312713-37:
(9*1)+(8*3)+(7*1)+(6*2)+(5*7)+(4*1)+(3*3)+(2*3)+(1*7)=113
113 % 10 = 3
So 1312713-37-3 is a valid CAS Registry Number.
1312713-37-3Relevant articles and documents
Deaminative Borylation of Aliphatic Amines Enabled by Visible Light Excitation of an Electron Donor–Acceptor Complex
Sandfort, Frederik,Strieth-Kalthoff, Felix,Klauck, Felix J. R.,James, Michael J.,Glorius, Frank
, p. 17210 - 17214 (2018)
A deaminative strategy for the borylation of aliphatic primary amines is described. Alkyl radicals derived from the single-electron reduction of redox-active pyridinium salts, which can be isolated or generated in situ, were borylated in a visible light-mediated reaction with bis(catecholato)diboron. No catalyst or further additives were required. The key electron donor–acceptor complex was characterized in detail by both experimental and computational investigations. The synthetic potential of this mild protocol was demonstrated through the late-stage functionalization of natural products and drug molecules.
