138769-30-9 Usage
Uses
Used in Pharmaceutical Industry:
N-(4-Chloro-3-pyridinyl)acetamide is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new drugs, potentially leading to innovative treatments for various medical conditions.
Used in Agrochemical Industry:
In the agrochemical industry, N-(4-Chloro-3-pyridinyl)acetamide is used as a precursor in the production of pesticides, insecticides, and herbicides. Its chemical properties make it suitable for creating effective compounds that protect crops from pests and enhance agricultural productivity.
Used in Chemical Research:
N-(4-Chloro-3-pyridinyl)acetamide is also utilized in chemical research for studying the properties and reactions of similar compounds. Its unique structure provides valuable insights into the behavior of related molecules, contributing to the advancement of chemical knowledge and the development of new applications.
Check Digit Verification of cas no
The CAS Registry Mumber 138769-30-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,6 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138769-30:
(8*1)+(7*3)+(6*8)+(5*7)+(4*6)+(3*9)+(2*3)+(1*0)=169
169 % 10 = 9
So 138769-30-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H7ClN2O/c1-5(11)10-7-4-9-3-2-6(7)8/h2-4H,1H3,(H,10,11)
138769-30-9Relevant academic research and scientific papers
Monoprotected l-Amino Acid (l-MPAA), Accelerated Bromination, Chlorination, and Iodination of C(sp2)?H Bonds by Iridium(III) Catalysis
Kathiravan, Subban,Nicholls, Ian A.
supporting information, p. 7031 - 7036 (2017/05/29)
Halogenated arenes are important structural motifs commonly found in biologically active molecules and used for a variety of transformations in organic synthesis. Herein, we report the mono-protected l-amino acid (l-MPAA) accelerated iridium(III)-catalyzed halogenation of (hetero)anilides at room temperature. This reaction constitutes the first example of an iridium(III)/l-MPAA-catalyzed general halogenation of (hetero)arenes through C(sp2)?H activation. Furthermore, we demonstrate the potential utility of our method through its use in the synthesis of a quinolone derivative.
A palladium-catalyzed regiospecific synthesis of N-aryl benzimidazoles
Zheng, Nan,Anderson, Kevin W.,Huang, Xiaohua,Nguyen, Hanh Nho,Buchwald, Stephen L.
, p. 7509 - 7512 (2008/09/17)
(Chemical Equation Presented) Highly tolerated: A catalytic method employing [Pd2(dba)3] and XPhos or RuPhos permits the efficient synthesis of N-aryl benzimidazoles in regioisomerically pure form starting from ortho-halo-anilides (see scheme), and tolerates a wide range of functional groups, dba = trans,trans-dibenzylideneacetone.
