23953-63-1 Usage
Uses
Since the provided materials do not specify the uses of 5-Methoxy-6-[(Z)-1-propenyl]-1,3-benzodioxole, it is not possible to list its applications based on the given information. However, it is important to note that the detailed properties, including physical and chemical properties, reactivity, toxicity, or applications, of this specific compound might vary and could be researched or experimented upon as required. It is also crucial to handle any chemical substances with appropriate safety measures.
Check Digit Verification of cas no
The CAS Registry Mumber 23953-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,9,5 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23953-63:
(7*2)+(6*3)+(5*9)+(4*5)+(3*3)+(2*6)+(1*3)=121
121 % 10 = 1
So 23953-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O3/c1-3-4-8-5-10-11(14-7-13-10)6-9(8)12-2/h3-6H,7H2,1-2H3/b4-3+
23953-63-1Relevant academic research and scientific papers
Total Synthesis of Carpacin and Its Geometric Isomer as a Cancer Chemopreventer
Tseng, Tsui-Hwa,Tsheng, Yen-Min,Lee, Yean-Jang,Hsu, Hsing-Ling
, p. 1165 - 1170 (2007/10/03)
Carpacin (1a), an antidepressant in Asiatic folk medicine from the Carpano tree, is achieved in which the longest linear sequence is only four steps in over all yield 67 percent from commercially available Sesamol. The key transformations in the synthesis are the selective palladium-catalyzed coupling reactions of aryl bromide with Grignard reagents. The first preparation of its geometric isomer (1b) is described. Highlights of the synthesis include Pd-ctalyzed coupling, selective hydrogenation, and Wittig reactions. Carpacin was examined as a potential inhibitor of carcinogenesis.
