1352523-17-1 Usage
Uses
Used in Pharmaceutical Synthesis:
Tert-butyl 2-(pyridin-4-yl)pyrrolidine-1-carboxylate is used as an intermediate in the synthesis of pharmaceuticals for its potential bioactivity, contributing to the development of new drugs with therapeutic benefits.
Used in Agrochemical Synthesis:
tert-Butyl 2-(pyridin-4-yl)pyrrolidine-1-carboxylate is also utilized as an intermediate in the synthesis of agrochemicals, where its bioactivity can be harnessed to create effective products for agricultural applications.
Used in Chemical Research:
Tert-butyl 2-(pyridin-4-yl)pyrrolidine-1-carboxylate serves as a building block in chemical research, enabling the creation of new compounds for various purposes, including the development of innovative materials and substances with unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1352523-17-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,5,2 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1352523-17:
(9*1)+(8*3)+(7*5)+(6*2)+(5*5)+(4*2)+(3*3)+(2*1)+(1*7)=131
131 % 10 = 1
So 1352523-17-1 is a valid CAS Registry Number.
1352523-17-1Relevant articles and documents
Native functionality in triple catalytic cross-coupling: sp3 C-H bonds as latent nucleophiles
Shaw, Megan H.,Shurtleff, Valerie W.,Terrett, Jack A.,Cuthbertson, James D.,MacMillan, David W.C.
, p. 1304 - 1308 (2016/07/06)
The use of sp3 C-H bonds - which are ubiquitous in organic molecules - as latent nucleophile equivalents for transition metal - catalyzed cross-coupling reactions has the potential to substantially streamline synthetic efforts in organic chemistry while bypassing substrate activation steps. Through the combination of photoredox-mediated hydrogen atom transfer (HAT) and nickel catalysis, we have developed a highly selective and general C-H arylation protocol that activates a wide array of C-H bonds as native functional handles for cross-coupling. This mild approach takes advantage of a tunable HAT catalyst that exhibits predictable reactivity patterns based on enthalpic and bond polarity considerations to selectively functionalize α-amino and α-oxy sp3 C-H bonds in both cyclic and acyclic systems.
