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2-methoxy-3-benzyloxyestra-1,3,5(10)-trien-17β-yl sulfamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

923029-65-6

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923029-65-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 923029-65-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,0,2 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 923029-65:
(8*9)+(7*2)+(6*3)+(5*0)+(4*2)+(3*9)+(2*6)+(1*5)=156
156 % 10 = 6
So 923029-65-6 is a valid CAS Registry Number.

923029-65-6Relevant academic research and scientific papers

2-methoxy estradiol analogs and method for preparation thereof and use

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Paragraph 0033; 0039; 0041, (2016/11/09)

The invention relates to a 2-methoxy-estradiol analogue and a preparation method and application thereof, aiming to solve the problem of preparation of the 2-methoxy-estradiol analogue and realize the application of the 2-methoxy-estradiol analogue to preparation of anti-tumor medicaments. The method comprises the following steps: dissolving 2-methoxy-3-benzyloxy-estradiol-1,3,5-(10)-triene-17beta-alcohol or 17beta-amine serving as a raw material into an organic solvent; in the presence of Lewis alkali, carrying out an acylation reaction on the raw materials and a compound (1) to obtain a 2-methoxy-3-benzyloxy-estradiol-1,3,5-(10)-triene-17beta-ester or 17beta-amide compound (2); carrying out a catalytic hydrogenation to obtain a compound (3); carrying out an acylation reaction or a hydrocarbylation reaction to obtain a compound, namely, the 2-methoxy-estradiol analogue (4), wherein a reaction formula is shown in the specifications. The preparation method of the 2-methoxy-estradiol analogue has the advantages of easiness, mild conditions and high yield, and can be effectively applied to development of anti-tumor medicaments.

2-Substituted estradiol bis-sulfamates, multitargeted antitumor agents: Synthesis, in vitro SAR, protein crystallography, and in vivo activity

Leese, Mathew P.,Leblond, Bertrand,Smith, Andrew,Newman, Simon P.,Di Fiore, Anna,De Simone, Giuseppina,Supuran, Claudiu T.,Purohit, Atul,Reed, Michael J.,Potter, Barry V. L.

, p. 7683 - 7696 (2007/10/03)

The anticancer activities and SARs of estradiol-17-O-sulfamates and estradiol 3,17-O,O-bis-sulfamates (E2bisMATEs) as steroid sulfatase (STS) inhibitors and antiproliferative agents are discussed. Estradiol 3,17-O,O-bis-sulfamates 20 and 21, in contrast t

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