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Ethyl 2-(2'-ethoxyoxoethyl)-4,6-dihydroxybenzoate is a complex organic compound with the chemical formula C13H16O6. It is a derivative of benzoic acid, featuring a benzene ring with two hydroxyl groups at the 4 and 6 positions, and an ethoxyoxoethyl group at the 2 position. ethyl 2-(2'-ethoxyoxoethyl)-4,6-dihydroxybenzoate is characterized by its ester linkage, which connects the benzoate group to an ethyl group. It is synthesized through a series of chemical reactions and is used in various applications, including as a chemical intermediate in the production of pharmaceuticals and other organic compounds. Due to its specific structure, it may exhibit unique properties such as solubility in organic solvents and potential reactivity with other chemical entities.

6121-80-8

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6121-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6121-80-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,2 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6121-80:
(6*6)+(5*1)+(4*2)+(3*1)+(2*8)+(1*0)=68
68 % 10 = 8
So 6121-80-8 is a valid CAS Registry Number.

6121-80-8Relevant academic research and scientific papers

Synthesis process of natural product Agrimonolide (I) racemate extracted from agrimonia pilosa

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, (2018/12/05)

The invention belongs to the field of chemical synthesis, and particularly relates to a total synthesis method of a natural product 6,8-dyhydroxyl-3-(4'-methoxyphenyl ethyl) isochroman-1-ketone (dl-Agrimonolide (I)) extracted from a plant agrimonia pilosa

Targeting the Hsp90 chaperone: Synthesis of novel resorcylic acid macrolactone inhibitors of Hsp90

Day, James E. H.,Sharp, Swee Y.,Rowlands, Martin G.,Aherne, Wynne,Workman, Paul,Moody, Christopher J.

supporting information; experimental part, p. 2758 - 2763 (2010/07/04)

A series of benzo-macrolactones has been prepared by chemical synthesis, and evaluated as inhibitors of heat shock protein 90 (Hsp90), an emerging attractive target for novel cancer therapeutic agents. A new synthesis of these resorcylic acid macrolactone analogues of the natural product radicicol is described in which the key steps are the acylation and ring opening of a homophthalic anhydride to give an isocoumarin, followed by a ring-closing metathesis to form the macrocycle. The methodology has been extended to a novel series of macrolactones incorporating a 1,2,3-triazole ring.

An improved synthesis of resorcylic acid macrolactone inhibitors of Hsp90

Day, James E. H.,Blake, Alexander J.,Moody, Christopher J.

scheme or table, p. 1567 - 1570 (2009/11/30)

A synthesis of resorcylic acid macrolactone analogues of the natural product radicicol is described in which the key steps are the acylation and ring opening of a homophthalic anhydride to give an isocoumarin, followed by a ring-closing metathesis to form

Condensation of Diethyl Acetonedicarboxylate. III. Isolation and Acylation of Diethyl Acetonedicarboxylate-Magnesium Complex

Yamato, Masatoshi,Kusunoki, Youichiro

, p. 1214 - 1220 (2007/10/02)

Diethyl acetonedicarboxylate (DADC)-magnesium complex, (DADC)2Mg (5b), was isolated from the reaction of DADC and MgCl2 with Et3N, or by the removal of coordination water from (DADC)2Mg*2H2O (5a).Compound 5b could be regarded as an intermediate in the sel

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