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10-(4-Fluoro-phenyl)-3-methyl-10H-pyrimido[4,5-b]quinoline-2,4-dione is a complex organic compound with a molecular formula of C18H12FN3O2. It is characterized by a pyrimido[4,5-b]quinoline core structure, which features a quinoline ring fused to a pyrimidine ring. The compound has a fluorophenyl group attached at the 10th position and a methyl group at the 3rd position. The 2,4-dione functional groups indicate the presence of two carbonyl groups at these positions, contributing to the compound's reactivity and potential applications. This chemical is often associated with pharmaceutical research due to its structural similarity to certain biologically active molecules, and it may be investigated for its potential therapeutic properties or as a chemical intermediate in the synthesis of more complex molecules.

76896-50-9

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76896-50-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76896-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,9 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76896-50:
(7*7)+(6*6)+(5*8)+(4*9)+(3*6)+(2*5)+(1*0)=189
189 % 10 = 9
So 76896-50-9 is a valid CAS Registry Number.

76896-50-9Downstream Products

76896-50-9Relevant academic research and scientific papers

Synthesis of 10-Arylpyrimidoquinoline-2,4(3H,10H)diones (10-Aryl-5-deazaflavins) and Their Use in Oxidations of Alcohols and Amines

Yoneda, Fumio,Tsukuda, Kinshiro,Shinozuka, Kazuo,Hirayama, Fumitoshi,Uekama, Kaneto,Koshiro, Akira

, p. 3049 - 3056 (2007/10/02)

Treatment of aryl-bis(6-anilino-3-methyluracil-5-yl)methanes, which were prepared by the condensation of 6-anilino-3-methyluracils with arylaldehydes, with diethyl azodicarboxylate (DAD) in the presence of sulfolane led to the formation of the corresponding 10-arylpyrimidoquinoline-2,4(3H,10H)-diones (10-aryl-5-deazaflavins).Heating of the methanes alone in sulfolane without DAD gave the corresponding 5-aryl-5-deazaalloxazines.The oxidizing abilities of the 10-aryl-5-deazaflavins thus obtained were examined from both kinetic and synthetic viewpoints.The oxidations of benzyl alcohol and benzylamine by these 5-deazaflavins have been shown to recycle automatically, and more than 100percent yield of benzaldehyde (based on the 5-deazaflavins) was obtained.Keywords - pyrimidoquinoline; 5-deazaflavin; alcohol oxidation; amine oxidation; diethyl azodicarboxylate; aryl-bis(6-anilinouracil-5-yl)methane; 5-deazaalloxazine; turn-over catalyst; biomimetic axidation.

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