67867-35-0 Usage
Description
(E)-2-(4-methoxyphenyl)-2-oxoacetaldehyde oxime is a chemical compound with the molecular formula C9H9NO3. It is an oxime derivative of acetaldehyde featuring a 4-methoxyphenyl group attached to the nitrogen atom. (E)-2-(4-methoxyphenyl)-2-oxoacetaldehyde oxime is significant in organic synthesis and medicinal chemistry, serving as a building block for the creation of various pharmaceuticals and biologically active molecules. Its oxime functional group renders it a versatile intermediate for the formation of oxime ethers, hydrazones, and other nitrogen-containing compounds. Furthermore, it holds potential as a reagent in the synthesis of heterocycles and complex organic molecules. In essence, (E)-2-(4-methoxyphenyl)-2-oxoacetaldehyde oxime is instrumental in the development of new drugs and compounds for a range of biological and therapeutic applications.
Uses
Used in Organic Synthesis:
(E)-2-(4-methoxyphenyl)-2-oxoacetaldehyde oxime is used as a building block for the synthesis of various pharmaceuticals and biologically active molecules. Its unique structure and oxime functional group contribute to its versatility in creating a wide array of compounds with potential applications in the medical field.
Used in Medicinal Chemistry:
In the realm of medicinal chemistry, (E)-2-(4-methoxyphenyl)-2-oxoacetaldehyde oxime is utilized as a key intermediate in the development of new drugs. Its ability to form oxime ethers, hydrazones, and other nitrogen-containing compounds makes it a valuable asset in the synthesis of complex organic molecules with therapeutic potential.
Used in the Synthesis of Heterocycles:
(E)-2-(4-methoxyphenyl)-2-oxoacetaldehyde oxime is also employed as a reagent in the synthesis of heterocycles, which are important components in many pharmaceuticals and natural products. Its involvement in this process aids in the creation of novel compounds with potential therapeutic properties.
Used in the Development of New Drugs:
(E)-2-(4-methoxyphenyl)-2-oxoacetaldehyde oxime plays a crucial role in the development of new drugs and compounds for various biological and therapeutic purposes. Its unique properties and reactivity make it an essential component in the design and synthesis of innovative pharmaceuticals aimed at treating a wide range of diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 67867-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,6 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67867-35:
(7*6)+(6*7)+(5*8)+(4*6)+(3*7)+(2*3)+(1*5)=180
180 % 10 = 0
So 67867-35-0 is a valid CAS Registry Number.
67867-35-0Relevant articles and documents
Single-Step Modular Synthesis of Unsaturated Morpholine N-Oxides and Their Cycloaddition Reactions
Son, Jongwoo,Kim, Ki Hwan,Mo, Dong-Liang,Wink, Donald J.,Anderson, Laura L.
supporting information, p. 3059 - 3063 (2017/03/14)
A single-flask procedure for the generation of α-keto-N-alkenylnitrones through a Chan–Lam coupling and subsequent spontaneous 6π electrocyclization of these intermediates for the synthesis of 2H-1,4-oxazine N-oxides has been developed for a variety of α-ketooximes and alkenylboronic acids. This transformation provides a new approach to C-substituted unsaturated morpholine derivatives that are poised to undergo further functionalization for the preparation of a diverse array of novel heterocyclic structures. The scope of the new method for the synthesis of 2H-1,4-oxazine N-oxides is discussed, in addition to initial studies describing the cycloaddition reactivity of these new heterocyclic intermediates.
THROMBOPOETIN RECEPTOR ACTIVATOR AND PROCESS FOR PRODUCING THE SAME
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Page/Page column 15-16, (2008/06/13)
A preventive, therapeutic or improving agent for diseases against which activation of the thrombopoietin receptor is effective or a platelet increasing agent, which contains a thrombopoietin receptor activator represented by the formula (1): [wherein each
An efficient route to 5,5″-diaryl-2,2′:6′,2″- terpyridines through 2,6-bis(1,2,4-triazin-3-yl)pyridines
Kozhevnikov, Valery N.,Kozhevnikov, Dmitry N.,Shabunina, Olga V.,Rusinov, Vladimir L.,Chupakhin, Oleg N.
, p. 1521 - 1523 (2007/10/03)
A new route to substituted 2,2′:6′,2″-terpyridines based on a new method for the synthesis of substituted 2,6-bis(1,2,4-triazin-3-yl) pyridines and their inverse electron demand Diels-Alder reaction is shown to be an efficient strategy for the synthesis of structurally diverse terpyridine ligands.
