23953-63-1 Usage
General Description
5-Methoxy-6-[(Z)-1-propenyl]-1,3-benzodioxole is a chemical compound belonging to the benzodioxoles group, characterized by a benzene ring fused to a 1,3-dioxole. As its name indicates, its structure involves a methoxy group at the 5-position and a propenyl group at the 6-position of the benzodioxole core. The mention of (Z) signifies that the double bond in the propenyl side chain has a cis configuration. 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. However, it is important 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 articles and documents
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.
