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6,11-Dihydro-5H-benzo[b]carbazole-6,11-dione is a chemical compound with the molecular formula C13H9NO2. It is a derivative of benzo[b]carbazole, a tricyclic aromatic compound consisting of a benzene ring fused to an indole ring. This specific compound features two carbonyl groups (C=O) at the 6 and 11 positions, and a fully saturated six-membered ring between the two nitrogen atoms. It is an organic compound with potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and properties. The compound is known for its stability and can be used as a building block in the creation of more complex molecules.

6451-05-4

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6451-05-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6451-05-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,5 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6451-05:
(6*6)+(5*4)+(4*5)+(3*1)+(2*0)+(1*5)=84
84 % 10 = 4
So 6451-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C23H17Cl2N3O3S/c1-12-3-4-13(22-26-18-11-15(25)6-8-20(18)31-22)9-17(12)27-23(32)28-21(29)16-10-14(24)5-7-19(16)30-2/h3-11H,1-2H3,(H2,27,28,29,32)

6451-05-4Downstream Products

6451-05-4Relevant academic research and scientific papers

Synthesis of Carbazolequinones by Formal [3 + 2] Cycloaddition of Arynes and 2-Aminoquinones

Guo, Jian,Kiran, I. N. Chaithanya,Reddy, R. Santhosh,Gao, Jiangsheng,Tang, Meiqiong,Liu, Yuyin,He, Yun

supporting information, p. 2499 - 2502 (2016/06/09)

A formal cycloaddition reaction for the synthesis of biologically and pharmaceutically important carbazolequinones via the annulation of aminoquinones with arynes has been developed. This practical and metal-free cascade reaction proceeds through successive C-C/C-N bond formations. Moreover, this novel method has been utilized for the concise synthesis of bioactive murrayaquinone A and koeniginequinone B and their analogues.

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