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2',3'-bis(methoxymethyloxy)-3,4,4',5-tetramethoxydiphenylcarbinol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

290347-54-5

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290347-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 290347-54-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,0,3,4 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 290347-54:
(8*2)+(7*9)+(6*0)+(5*3)+(4*4)+(3*7)+(2*5)+(1*4)=145
145 % 10 = 5
So 290347-54-5 is a valid CAS Registry Number.

290347-54-5Relevant academic research and scientific papers

Hydroxyphenstatin and the prodrugs thereof

-

, (2008/06/13)

The benzophenone derivative of combretastatin A-1, designated “hydroxyphenstatin”, was synthesized by compiling a protected bromobenzene and a benzaldehyde to form a benzhydrol which was subsequently oxidized to the ketone. Hydroxyphenstatin was converted

Antineoplastic agents. 443. Synthesis of the cancer cell growth inhibitor hydroxyphenstatin and its sodium diphosphate prodrug

Pettit, George R.,Grealish, Matthew P.,Herald, Delbert L.,Boyd, Michael R.,Hamel, Ernest,Pettit, Robin K.

, p. 2731 - 2737 (2007/10/03)

A structure - activity relationship (SAR) study of the South African willow tree (Combretum caffrum) antineoplastic constituent combretastatin A-4 (3b) led to the discovery of a potent cancer cell growth inhibitor designated phenstatin (5a). This benzophenone derivative of combretastatin A-4 showed remarkable antineoplastic activity, and the benzophenone derivative of combretastatin A-1 was therefore synthesized. The benzophenone, designated hydroxyphenstatin (6a), was synthesized by coupling of a protected bromobenzene and a benzaldehyde to give the benzhydrol with subsequent oxidation to the ketone. Hydroxyphenstatin was converted to the sodium phosphate prodrug (6e) by a dibenzyl phosphite phosphorylation and subsequent benzyl cleavage (6a → 6d → 6e). While hydroxyphenstatin (6a) was a potent inhibitor of tubulin polymerization with activity comparable to that of combretastatin A-1 (3a), the phosphorylated derivative (6e) was inactive.

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