61190-46-3 Usage
Uses
Used in Pharmaceutical Industry:
(E)-6,7-Dihydrobenzofuran-4(5H)-one oxime is used as an intermediate in the synthesis of pharmaceutical compounds for various therapeutic applications. Its unique structure and reactivity make it a valuable component in the development of new drugs.
Used in Organic Synthesis:
(E)-6,7-Dihydrobenzofuran-4(5H)-one oxime is used as a building block in organic synthesis, allowing chemists to create a variety of complex molecules with potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.
Used in Research and Development:
(E)-6,7-Dihydrobenzofuran-4(5H)-one oxime is used as a research compound to study its biological activities and potential therapeutic applications. Its unique structure and properties make it an interesting candidate for further investigation in the development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 61190-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,9 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61190-46:
(7*6)+(6*1)+(5*1)+(4*9)+(3*0)+(2*4)+(1*6)=103
103 % 10 = 3
So 61190-46-3 is a valid CAS Registry Number.
61190-46-3Relevant academic research and scientific papers
CXCR2 ANTAGONIST
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Paragraph 0104-0105; 0107, (2020/11/23)
A compound as a CXCR2 antagonist and an application thereof in preparing a drug as a CXCR2 antagonist. In particular, the present invention relates to a compound represented by formula (II) or an isomer or pharmaceutically acceptable salt thereof.
AMINO-QUINOLINES AS KINASE INHIBITORS
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Paragraph 0180; 0181, (2015/09/23)
Disclosed are quinoline compounds having the formula: wherein R1, R2 and A are as defined herein, and methods of making and using the same.
Regioselective synthesis of several heterocyclic fused azepines using diisobutylaluminum hydride
Cho, Hidetsura,Murakami, Kengo,Nakanishi, Hiroyuki,Isoshima, Hirotaka,Hayakawa, Kazuhide,Uchida, Itsuo
, p. 919 - 927 (2007/10/03)
5,6,7,8-Tetrahydrothieno[3,2-b]azepine,5,6,7,8-tetrahydro-1H-furo[3,2-b] azepine, and 1,4,5,6,7,8-hexahydropyrrolo[3,2-b]azepine were synthesized by the ring expansion reaction of heterocyclic fused cyclohexanone oximes with diisobutylaluminum hydride (DIBAH). The mechanism of the reaction was different from that of Beckmann rearrangement.
