7509-61-7 Usage
Description
(2E)-N-(2-Ethylphenyl)-2-(hydroxyimino)acetamide is an organic compound belonging to the hydroxylamine family, characterized by its molecular formula C12H15NO2. It is a white to off-white crystalline powder that exhibits solubility in organic solvents such as methanol and ethanol. This versatile chemical serves as a valuable precursor in organic synthesis, enabling the creation of various functional groups and heterocyclic compounds, as well as contributing to the development of biologically active molecules.
Uses
Used in Organic Synthesis:
(2E)-N-(2-Ethylphenyl)-2-(hydroxyimino)acetamide is utilized as a reagent in the preparation of a wide range of organic compounds. Its ability to act as a versatile precursor allows for the synthesis of different functional groups, making it a valuable component in the creation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2E)-N-(2-Ethylphenyl)-2-(hydroxyimino)acetamide is employed as a building block for the development of heterocyclic compounds and other biologically active molecules. Its role in the synthesis of such compounds contributes to the advancement of new drug candidates and therapeutic agents.
Used in Chemical Research:
(2E)-N-(2-Ethylphenyl)-2-(hydroxyimino)acetamide also serves as an important tool in chemical research, where it is used to explore novel reactions and mechanisms. Its unique properties and reactivity make it a useful probe for understanding the behavior of various organic systems and advancing the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 7509-61-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7509-61:
(6*7)+(5*5)+(4*0)+(3*9)+(2*6)+(1*1)=107
107 % 10 = 7
So 7509-61-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O2/c1-2-8-5-3-4-6-9(8)12-10(13)7-11-14/h3-7,14H,2H2,1H3,(H,12,13)
7509-61-7Relevant articles and documents
Palladium(II)/N-Heterocyclic Carbene Catalyzed One-Pot Sequential α-Arylation/Alkylation: Access to 3,3-Disubstituted Oxindoles
Reddy Panyam, Pradeep Kumar,Ugale, Bharat,Gandhi, Thirumanavelan
supporting information, p. 7622 - 7632 (2018/06/22)
Rationally designed fluorene-based mono- and bimetallic Pd-PEPPSI complexes were synthesized and demonstrated to be effective for the one-pot sequential α-arylation/alkylation of oxindoles. This streamlined approach offers efficient access to functionalized 3,3-disubstituted oxindoles in excellent yields (up to 89%) under mild reaction conditions.
Methods and Compositions for Selectin Inhibition
-
Page/Page column 22, (2008/12/04)
The present teachings relate to novel compounds of formula I: wherein the constituent variables are as defined herein. Compounds of the present teachings can act as antagonists of the mammalian adhesion proteins known as selecting. Methods for treating or preventing selectin-mediated disorders are provided, which include administration of these compounds in a therapeutically effective amount.
Condensed bridgehead nitrogen heterocyclic systems: Synthesis and antimicrobial activity of thiazolo[3′, 2′: 2, 3]-as-triazino[5, 6-b]indoles and isomeric thiazolo[2′, 3′: 3, 4]-as-triazino[5, 6-b]indoles
Mohan, Jag,Anupama
, p. 628 - 630 (2007/10/03)
2, 3-Dihydro-6-ethyl-5H-as-triazino[5, 6-b]indole-3-thione 4 on condensation with α-haloketone gives 3-aroylmethylthio-6-ethyl-5H-as-triazino[5, 6-b]indolehydrobromide 5 which on PPA catalyzed cyclization furnishes 3-aryl-9-ethylthiazolo[3′, 2′: 2, 3]-as-
