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(E)-methyl 6-[2-(tert-butyldimethylsiloxy)-3-methoxy-3-oxoprop-1-en-1-yl]-2-methoxy-3-(methoxymethoxy)-4-{1-[(4-methoxyphenyl)dimethylsilyl]-3-oxo-4-[1,4,5,6,8-pentamethoxy-3-(methoxymethoxy)naphthalen-2-yl]butyl}benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1622104-33-9

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1622104-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1622104-33-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,2,1,0 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1622104-33:
(9*1)+(8*6)+(7*2)+(6*2)+(5*1)+(4*0)+(3*4)+(2*3)+(1*3)=109
109 % 10 = 9
So 1622104-33-9 is a valid CAS Registry Number.

1622104-33-9Relevant academic research and scientific papers

A convergent total synthesis of the telomerase inhibitor (±)-γ-rubromycin

Wilsdorf, Michael,Reissig, Hans-Ulrich

, p. 4332 - 4336 (2014/05/06)

The total synthesis of the human telomerase inhibitor γ-rubromycin in its racemic form was accomplished in 3.8 % overall yield. The key feature of this synthesis is an efficient acid-catalyzed spiroketalization for the construction of the spiroketal core. The required electronically well-balanced spiroketal precursor was obtained by the convergent assembly of a naphthyl-substituted aldehyde, an α-methoxyallyl-γ-silyl-substituted phosphonate as the central C3 building block, and a highly functionalized aryl Grignard reagent. Another key feature is the late-stage construction of the isocoumarin moiety and a simultaneous protodesilylation furnishing the known methyl aryl ether protected precursor of γ-rubromycin. 3 building blocks + 3 acids→natural product: After the assembly of the crucial precursor from three highly functionalized building blocks, the pivotal spiroketalization was achieved with trifluoromethanesulfonic acid, the isocoumarin formation with fluoroboric acid, and the O-demethylation with the Lewis acid boron tribromide. (±)-γ-Rubromycin was thus synthesized in 18 steps with an overall yield of 3.8 % from commercially available precursors.

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