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(4aR,8aS)-2-methoxy-6,8a-dimethyl-4a,5,8,8a-tetrahydronaphthalene-1,4-dione is a complex organic compound belonging to the tetrahydronaphthalene-1,4-dione class. It features a four-membered ring structure with two carbon atoms and two oxygen atoms, along with a methoxy group and multiple methyl groups. These structural elements suggest that the compound may exhibit aromatic and hydrophobic characteristics.

6630-44-0

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6630-44-0 Usage

Uses

The specific applications of (4aR,8aS)-2-methoxy-6,8a-dimethyl-4a,5,8,8a-tetrahydronaphthalene-1,4-dione would be contingent upon its chemical, physical, biological, and pharmaceutical properties. Given its complex structure, it may have potential uses in various industries, such as pharmaceuticals, materials science, or as an intermediate in chemical synthesis. However, without more detailed information on its properties and activities, it is not possible to provide a comprehensive list of uses. Further research and development would be necessary to determine the compound's practical applications and benefits in different fields.

Check Digit Verification of cas no

The CAS Registry Mumber 6630-44-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6630-44:
(6*6)+(5*6)+(4*3)+(3*0)+(2*4)+(1*4)=90
90 % 10 = 0
So 6630-44-0 is a valid CAS Registry Number.

6630-44-0Downstream Products

6630-44-0Relevant academic research and scientific papers

Asymmetric quinone-based Diels-Alder reactions

Engler,Letavic,Takusagawa

, p. 6731 - 6734 (2007/10/02)

Asymmetric Diels-Alder reactions of 2-methoxy-1,4-benzoquinones utilizing a chiral Ti(IV) complex as a Lewis acid promoter are reported.

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