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1,4-Methano-5H-oxazolo[3,2-a]quinolin-2(1H)-one, 3a,4-dihydro-1-methyl-3a-phenyl- is a complex organic compound with a unique chemical structure. It is characterized by a fused oxazole and quinoline ring system, with a methyl group attached to the 1-position and a phenyl group at the 3a-position. 1,4-Methano-5H-oxazolo[3,2-a]quinolin-2(1H)-one, 3a,4-dihydro-1-methyl-3a-phenyl- is a derivative of the parent compound 1,4-methano-5H-oxazolo[3,2-a]quinolin-2(1H)-one, which is a heterocyclic compound containing both oxygen and nitrogen atoms in its structure. The specific arrangement of atoms and functional groups in 1,4-Methano-5H-oxazolo[3,2-a]quinolin-2(1H)-one, 3a,4-dihydro-1-methyl-3a-phenyl- may confer unique chemical and biological properties, making it a potential candidate for further study in various fields, such as pharmaceuticals or materials science.

77219-98-8

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77219-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77219-98-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,1 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77219-98:
(7*7)+(6*7)+(5*2)+(4*1)+(3*9)+(2*9)+(1*8)=158
158 % 10 = 8
So 77219-98-8 is a valid CAS Registry Number.

77219-98-8Downstream Products

77219-98-8Relevant academic research and scientific papers

Regiochemistry of Intramolecular Munchnone Cycloadditions: Preparative and Mechanistic Implications

Padwa, Albert,Gingrich, Henry L.,Lim, Richard

, p. 2447 - 2456 (2007/10/02)

A series of munchnone derivatives containing an internal ? bond were generated in situ by treating several N-(o-allylphenyl)alanines with acetic anhydride.The major product obtained corresponded to intramolecular 1,3-dipolar cycloaddition of the mesoionic

Regiochemical aspects associated with the intramolecular 1,3-dipolar cycloaddition reactions of munchnone derivatives

Padwa, Albert,Gingrich, Henry L.,Lim, Richard

, p. 3419 - 3422 (2007/10/02)

The regioselectivity of the internal cycloaddition of a series of N-(o-allylphenyl) substituted munchnones has been found to be markedly dependent on the substituent groups present.

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