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2-[2-(2,6-dimethoxyphenoxy)ethyl]-1H-isoindole-1,3(2H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87780-28-7

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87780-28-7 Usage

Molecular weight

341.35 g/mol
The total mass of a single molecule of the compound is 341.35 grams per mole.

Chemical structure

Complex structure containing isoindole and phenoxy moieties
The compound is composed of two main structural units, an isoindole ring and a phenoxy ring, connected through an ethyl bridge.

Synthetic organic compound

Potential applications in medicinal chemistry and drug development
The compound is artificially synthesized and may have potential uses in the creation of new medications and therapies.

Further research needed

Specific properties, uses, and potential effects
More studies and analysis are required to determine the exact characteristics, applications, and possible effects of the compound on biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 87780-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,8 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87780-28:
(7*8)+(6*7)+(5*7)+(4*8)+(3*0)+(2*2)+(1*8)=177
177 % 10 = 7
So 87780-28-7 is a valid CAS Registry Number.

87780-28-7Relevant academic research and scientific papers

Method for synthesizing asymmetric C-O coupled compound and application of asymmetric C-O coupled compound

-

Paragraph 0221; 0226, (2016/10/07)

The invention discloses a method for synthesizing an asymmetric C-O coupled compound and application of the asymmetric C-O coupled compound and belongs to the technical field of chemical synthesis. According to the method, a compound represented by a form

Some potential α-adrenoreceptor blocking 1,4-benzodioxanes and 2,6-dimethoxyphenoxyethylamines

Dewar,Kapur,Mottram

, p. 286 - 290 (2007/10/02)

The synthesis and α-adrenoreceptor blocking activity of a series of 1,4-benzodioxanes and 2,6-dimethoxyphenoxyethylamines has been described. A number of analogues exhibited α-blockade, but none approached the potency of the benzodioxane WB 4101. Some mem

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