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"12-Ethyl-2,3,4,5,6,7-hexahydro-2-methyl-1,5-methano-1H-azocino[4,3-b]indol-6-ol" is a complex organic compound with a molecular formula of C18H23NO. It is a derivative of azocinoindol, a type of indole alkaloid, and features a hexahydro ring system with a methyl group at position 2 and an ethyl group at position 12. The compound also has a methano bridge connecting positions 1 and 5, and a hydroxyl group at position 6. This chemical structure is characteristic of certain natural products and may have potential applications in pharmaceutical or chemical research. However, without specific context or further information, it is difficult to provide a detailed summary of its properties, synthesis, or uses.

2744-46-9

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2744-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2744-46-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,4 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2744-46:
(6*2)+(5*7)+(4*4)+(3*4)+(2*4)+(1*6)=89
89 % 10 = 9
So 2744-46-9 is a valid CAS Registry Number.

2744-46-9Downstream Products

2744-46-9Relevant academic research and scientific papers

Stereoselective Total Synthesis of (±)-Dasycarpidol and (±)-Dasycarpidone

Patir, Süleyman,Tezeren, Mustafa A.,Salih, Bekir,Ertürk, Erkan

, p. 4175 - 4180 (2016/11/26)

The protecting-group-free and scalable total syntheses of (±)-dasycarpidol and (±)-dasycarpidone, as well as the formal total synthesis of (±)-uleine, are presented starting from a common tetrahydrocarbazole-fused lactone that is conveniently prepared on multigram scale. The key azocino[4,3-b]indole skeleton is constructed via the DDQ-mediated dehydrogenative cyclization of a tetrahydrocarbazole derivative possessing an amide side chain. The syntheses of the target natural products are accomplished in high yields and in a few steps by employing readily available conventional reagents.

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