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9H-Azuleno[1,2,3-ij]isoquinolin-9-one,4,5,6,- 10-tetramethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74684-11-0

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74684-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74684-11-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,8 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74684-11:
(7*7)+(6*4)+(5*6)+(4*8)+(3*4)+(2*1)+(1*1)=150
150 % 10 = 0
So 74684-11-0 is a valid CAS Registry Number.

74684-11-0Downstream Products

74684-11-0Relevant academic research and scientific papers

Total synthesis of tropoloisoquinolines: Imerubrine, isoimerubrine, and grandirubrine

Lee, Jae Chol,Cha, Jin Kun

, p. 3243 - 3246 (2007/10/03)

A unified, ready access to the tropoloisoquinoline alkaloids imerubrine (1), grandirubrine (2), and isoimerubrine (3) is delineated and features sequential application of the intramolecular Diels - Alder reaction of an acetylene-tethered oxazole and the [

Total synthesis of granditropone, grandirubrine, imerubrine, and isoimerubrine

Boger, Dale L.,Takahashi, Kanji

, p. 12452 - 12459 (2007/10/03)

Concise total syntheses of the naturally occurring tropoloisoquinolines grandirubrine (1), imerubrine (2), and isoimerubrine (3) are detailed. The regioselective total synthesis of grandirubrine (1) is based on the [4 + 2]cycloaddition reaction of the α-p

Preparation And Antileukemic Activity Of Congeners Of Tropoloisoquinoline Alkaloids From Abuta Concolor

Itokawa, Hideji,Matsumoto, Kouji,Morita, Hiroshi,Takeya, Koichi

, p. 1025 - 1032 (2007/10/02)

Antileukemic tropoloisoquinoline alkaloids, pareirubine A (1) and grandirubrine (2), at first have been isolated from Abuta concolor (Menispermaceae).Methylation of 1 and 2, existing in solution as a mixture of tautomers gave the corresponding four methyl derivatives (3 - 6).Thioimerubrine (7) and thioisoimerubrine (8) were prepared by the nucleophilic substitutions of the methoxyl groups at C-11 and -10, respectively.Acetylation of 1 and 2 produced the corresponding mono-acetyl tautomers (9 and 10).Antileukemic activity of these derived tropoloisoquinoline alkaloids is also reported.

GRANDIRUBRINE, A NEW TROPOLOISOQUINOLINE ALKALOID

Menachery, Mary D.,Cava, Michael P.

, p. 943 - 945 (2007/10/02)

Grandirubrine, a new alkaloid from Abuta grandifolia (Martius) Sandwith (Menispermaceae), has been assigned the tropoloisoquinoline structure I.

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