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"Z-1-(3-benzyloxy-4-methoxyphenyl)-1-methoxycarbonyl-2-(3,4,5-trimethoxyphenyl)ethene" is a complex organic compound characterized by its unique molecular structure. It features a phenyl group with a benzyloxy and methoxy substituent at the 3rd and 4th positions, respectively. The compound also includes a methoxycarbonyl group, which is a derivative of a carboxylic acid. Additionally, it has a trimethoxyphenyl group, indicating three methoxy groups attached to a phenyl ring. The molecule is further defined by an ethene bridge connecting these two distinct phenyl groups, with the Z-configuration indicating the geometric arrangement of the substituents around the double bond. Z-1-(3-benzyloxy-4-methoxyphenyl)-1-methoxycarbonyl-2-(3,4,5-trimethoxyphenyl)ethene is likely to be found in the realm of synthetic chemistry, potentially used in the synthesis of pharmaceuticals, dyes, or other specialty chemicals due to its intricate structure and functional groups.

89356-71-8

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89356-71-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89356-71-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,5 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89356-71:
(7*8)+(6*9)+(5*3)+(4*5)+(3*6)+(2*7)+(1*1)=178
178 % 10 = 8
So 89356-71-8 is a valid CAS Registry Number.

89356-71-8Relevant academic research and scientific papers

Biosynthesis. Part 26. Synthetic Studies of Structural Modification of Late Biosynthetic Precursors for Colchicine

Battersby, Alan R.,McDonald, Edward,Stachulski, Andrew V.

, p. 3053 - 3064 (2007/10/02)

The latter part of the natural pathway to colchicine is known to involve conversion of phenethyltetrahydroisoquinoline (2) by phenol oxidation into a dienone (O-methylandrocymbine) (4), the dienone subsequently undergoing ring-expansion to generate the tr

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