177744-83-1 Usage
Uses
Used in Pharmaceutical Industry:
N-(3-Hydroxypyridin-3-yl)pivalamide is used as a potential drug candidate for the development of new pharmaceuticals. Its unique structure and properties may contribute to the discovery of novel therapeutic agents with specific biological activities.
Used in Chemical Industry:
N-(3-Hydroxypyridin-3-yl)pivalamide is used as a building block for the synthesis of other organic compounds. Its versatile chemical structure allows for further functionalization and modification, enabling the creation of a wide range of chemical products.
Used in Research and Investigation:
N-(3-Hydroxypyridin-3-yl)pivalamide is used as a subject of research in the fields of medicinal chemistry and chemical biology. Its structure and properties make it an interesting target for studying the interactions between small molecules and biological systems, potentially leading to new insights and applications in drug discovery and development.
Used as a Reagent in Organic Synthesis:
N-(3-Hydroxypyridin-3-yl)pivalamide is used as a reagent in organic synthesis processes. Its unique functional groups and chemical properties can be utilized in various synthetic reactions, contributing to the preparation of complex organic molecules and compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 177744-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,7,7,4 and 4 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 177744-83:
(8*1)+(7*7)+(6*7)+(5*7)+(4*4)+(3*4)+(2*8)+(1*3)=181
181 % 10 = 1
So 177744-83-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H16N2O2/c1-9(2,3)8(13)12-10(14)5-4-6-11-7-10/h4,6-7,14H,5H2,1-3H3,(H,12,13)
177744-83-1Relevant academic research and scientific papers
Henry,Sánchez,Sabatié,Bénéteau,Guillaumet,Pujol
, p. 2405 - 2412 (2006)
The title compounds having different substituents on the heterocyclic framework were prepared by several methods from 2-acetamido-3-hydroxypyridine. The condensation of 2-protected-amino-3-hydroxypyridine with 2-chloroacrylonitrile or ethyl 2,3-dibromopro
Henry,Guillaumet,Pujol
, p. 1465 - 1468 (2004)
A novel short and enantioselective synthetic approach to pyridobenzoxazines is reported in which (R)- and (S)-3-(hydroxymethyl)-3,4- dihydro-2H-pyrido[3,2-b][1,4]oxazine were first synthesized from readily available chiral glycidyl derivatives.
