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Benzeneacetonitrile, 3,4-dimethoxy-α-(phenylmethylene)-, also known as 3,4-dimethoxybenzeneacetonitrile or 3,4-dimethoxy-α-phenylmethyleneacetonitrile, is an organic compound with the chemical formula C15H13NO2. It is a derivative of benzeneacetonitrile, featuring a phenylmethylene group (C6H5-CH=) attached to the α-carbon of the acetonitrile moiety. The compound has two methoxy groups (-OCH3) attached to the 3rd and 4th carbon atoms of the benzene ring, which contribute to its unique chemical properties. Benzeneacetonitrile, 3,4-dimethoxy-a-(phenylmethylene)- is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Its structure and reactivity make it a valuable building block in organic chemistry, particularly in the preparation of complex molecules with potential applications in various industries.

5508-10-1

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5508-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5508-10-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,0 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5508-10:
(6*5)+(5*5)+(4*0)+(3*8)+(2*1)+(1*0)=81
81 % 10 = 1
So 5508-10-1 is a valid CAS Registry Number.

5508-10-1Relevant academic research and scientific papers

PHENANTHROINDOLIZIDINE DERIVATIVE AND NF B INHIBITOR CONTAINING SAME AS ACTIVE INGREDIENT

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Page/Page column 14; 15, (2011/08/08)

A novel compound having an excellent NFκB inhibitory effect is provided. Specifically disclosed is a compound represented by the following formula (1) or a salt thereof: wherein, R1 represents a hydrogen atom, a lower alkyl group, or the like;

Asymmetric synthesis of phenanthroindolizidine alkaloids with hydroxyl group at the C14 position and evaluation of their antitumor activities

Ikeda, Takashi,Yaegashi, Takashi,Matsuzaki, Takeshi,Hashimoto, Syusuke,Sawada, Seigo

scheme or table, p. 342 - 345 (2011/02/27)

The asymmetric total synthesis of the strongly cytotoxic phenanthroindolizidine alkaloid 3 was achieved. Using the same route, various derivatives were also synthesized. Cytotoxicity of those synthetic compounds was evaluated and compounds 19, 23, and 27

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