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4,5-dimethoxyphthalimide is a chemical compound with the molecular formula C10H9NO4. It is a derivative of phthalimide, featuring two methoxy groups attached to the 4 and 5 positions of the phthalimide ring. This organic compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in the production of dyes and pigments. The presence of the methoxy groups enhances the solubility and reactivity of the compound, making it a valuable intermediate in organic synthesis. 4,5-dimethoxyphthalimide is typically synthesized through the reaction of phthalic anhydride with methanol in the presence of a catalyst, and it can be further functionalized to yield a range of products. Its stability, reactivity, and versatility make it an important building block in the chemical industry.

4764-20-9

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4764-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4764-20-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,6 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4764-20:
(6*4)+(5*7)+(4*6)+(3*4)+(2*2)+(1*0)=99
99 % 10 = 9
So 4764-20-9 is a valid CAS Registry Number.

4764-20-9Relevant academic research and scientific papers

Synthesis method of phthalimide and phenyl ring-substituted phthalimide derivative

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Paragraph 0013; 0017; 0018; 0020; 0023; 0028, (2017/08/25)

The invention provides a synthesis method of phthalimide and a phenyl ring-substituted phthalimide derivative. The synthesis method comprises that aromatic ketone and ammonia gas or an ammonia gas precursor as substrates and air or oxygen as an oxygen source undergo a reaction under catalyst action and liquid phase conditions to produce phthalimide and a phenyl ring-substituted phthalimide derivative. The synthesis method is mild, realizes high oxidation efficiency and a high product yield, utilizes oxygen or air as an oxygen source, is economic and eco-friendly and has a good application prospect.

Synthesis and biological activity of C-3' ortho dihydroxyphthalimido cephalosporins

Baudart,Hennequin

, p. 1458 - 1470 (2007/10/02)

A series of C-3' ortho dihydroxyphthalimido cephalosporins 3~7 has been prepared by reaction of C-3' aminomethyl cephalosporin 411) with the corresponding N carboethoxyphthalimides 23 ~ 25, 37, 38. These new caphalosporins exhibit excellent in vitro Gram-negative activities, including Pseudomonas aeruginosa, excellent β-lactamases stability and pharmacokinetics equivalent or better than ceftriaxone.

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