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2(1H)-Cycloheptimidazolone, 1-(4-methoxyphenyl)-, is a chemical compound with the molecular formula C14H14N2O2. It is a derivative of cycloheptimidazolone, featuring a 4-methoxyphenyl group attached to the 1-position of the imidazolone ring. 2(1H)-Cycloheptimidazolone, 1-(4-methoxyphenyl)- is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting various biological pathways. Its structure provides a unique combination of aromatic and heterocyclic moieties, which can influence its reactivity and interactions with biological targets. The compound's properties, such as solubility and stability, can be further explored for its suitability in medicinal chemistry and drug design.

3336-90-1

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3336-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3336-90-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,3 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3336-90:
(6*3)+(5*3)+(4*3)+(3*6)+(2*9)+(1*0)=81
81 % 10 = 1
So 3336-90-1 is a valid CAS Registry Number.

3336-90-1Downstream Products

3336-90-1Relevant academic research and scientific papers

Photoreactions of 3-tosyl- and 6-tosyldihydro-1,3-diazaazulanones to form 1,3-diazaazulanones and ionic pairs between p-toluenesulfonate anion and 1,3-diazadihydroazulanone cations

Saito, Katsuhiro,Kunisada, Tomoko,Ishiguro, Hiroyuki,Sato, Michie,Doi, Tadayuki

, p. 2315 - 2324 (2007/10/03)

A solvent effect was found on the photoreactions of 1-aryl-3-tosyldihydro-1,3-diazaazulanones with a low pressure mercury lamp. Thus, ion pairs between p-toluenesulfonate anion and the corresponding 1-aryl-1,3-diazadihydroazulanone cations were afforded b

Photoreactions of N-tosyldihydrodiazaazulanones to form diazaazulanones and ionic pairs between p-toluenesulfonate anion and tropyliumions

Doi, Tadayuki,Ishiguro, Hiroyuki,Sato, Michie,Saito, Katsuhiro

, p. 1775 - 1778 (2007/10/03)

Low pressure mercury lamp irradiations of N-aryl-N'- tosyldihydrodiazaazulanones in acetonitrile afforded the corresponding N- aryldiazaazulanones. Analogous photoreactions but using tetrahydrofuran as a solvent gave ion pairs between p-toluenesulfonate (

-TYPE CYCLOADDITION REACTIONS OF N-ARYL-2,4,6-CYCLOHEPTATRIENE-1-IMINES AND 2,4,6-CYCLOHEPTATRIENE-1-THIONE WITH p-TOLUENESULFONYL ISOCYANATE: FORMATION OF 1,3-DIAZAAZULANONES

Ito, Kazuaki,Saito, Katsuhiro,Takeuchi, Shigeyuki,Takahashi, Kensuke

, p. 1415 - 1422 (2007/10/02)

Reactions of N-aryl-2,4,6-cycloheptatriene-1-imines and 2,4,6-cycloheptatriene-1-thione with p-toluenesulfonyl isocyanate gave -type cycloadducts in good yields.Eliminations of tosyl groups and dehydrogenations of the adducts afforded 1,3-diazaazulan

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