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Isoquinoline, 1,2,3,4-tetrahydro-5,6,7-trimethoxy-1-[(4-methoxyphenyl)methyl]-2-methyl- is a complex organic compound belonging to the isoquinoline family. It is characterized by a tetrahydroisoquinoline core, with three methoxy groups attached at positions 5, 6, and 7, and a 4-methoxyphenylmethyl group connected to the 1-position. Additionally, a methyl group is present at the 2-position. Isoquinoline, 1,2,3,4-tetrahydro-5,6,7-trimethoxy-1-[(4-methoxyphenyl)methyl]-2-meth yl- is known for its potential applications in pharmaceuticals and as a precursor in the synthesis of various bioactive molecules. Its structure provides a foundation for further chemical modifications, making it a valuable intermediate in organic synthesis.

4668-07-9

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4668-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4668-07-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4668-07:
(6*4)+(5*6)+(4*6)+(3*8)+(2*0)+(1*7)=109
109 % 10 = 9
So 4668-07-9 is a valid CAS Registry Number.

4668-07-9Downstream Products

4668-07-9Relevant academic research and scientific papers

Synthesis and Evaluation of Analogues of (Z)-1-(4-Methoxyphenyl)-2-(3,4,5-trimethoxyphenyl)ethene as Potential Cytotoxic and Antimitotic Agents

Cushman, Mark,Nagatarathnam, Dhanapalan,Gopal, D.,He, Hu-Ming,Lin, Chii M.,Hamel, Ernest

, p. 2293 - 2306 (2007/10/02)

A series of stilbenes has been prepared and tested for cytotoxicity in the five human cancer cell lines A-549 non-small cell lung, MCF-7 breast, HT-29 colon, SKMEL-5 melanoma, and MLM melanoma.The cis stilbenes 6a-f proved to be cytotoxic in all five cell

A BIOMIMETIC SYNTHESIS OF (+/-)-TETRAHYDROTAKATONINE, (+/-)-O-METHYLGIGANTINE, AND TEHAUNINE

Hara, Hirohi,Tsunashima, Akira,Shinoki, Hiroshi,Hoshino, Osamu,Umezawa, Bunsuke

, p. 293 - 296 (2007/10/02)

Treatment of 7-acetoxy-7-methoxy-2-methyl-6-oxo-Δ4a,5,8,8a-hexahydroisoquinolines (6a-c) with conc.H2SO4 in Ac2O and subsequent hydrolysis followed by methylation produced the title alkaloids (9a-c), although in low yields.

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