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2,3,4-Furantricarboxylic acid, 5-(dimethylamino)-, trimethyl ester (9CI) is a chemical compound with a molecular formula C13H17NO4. It is an ester derivative of furantricarboxylic acid, featuring a furan ring with carboxylic acid and dimethylamino functional groups. 2,3,4-Furantricarboxylic acid, 5-(dimethylamino)-, trimethyl ester (9CI) is known for its potential applications in various fields, including pharmaceuticals, agrochemicals, organic chemistry, and materials science.

191085-54-8

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191085-54-8 Usage

Uses

Used in Pharmaceutical Industry:
2,3,4-Furantricarboxylic acid, 5-(dimethylamino)-, trimethyl ester (9CI) is used as an intermediate for the synthesis of pharmaceutical compounds. Its unique structure and functional groups make it a valuable building block in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 2,3,4-Furantricarboxylic acid, 5-(dimethylamino)-, trimethyl ester (9CI) serves as an intermediate for the synthesis of agrochemicals. Its properties can be harnessed to create effective pesticides, herbicides, or other agricultural chemicals that contribute to crop protection and yield enhancement.
Used in Organic Chemistry Research:
2,3,4-Furantricarboxylic acid, 5-(dimethylamino)-, trimethyl ester (9CI) is utilized in organic chemistry research for its potential applications in the synthesis of various organic compounds. Its unique structure allows for further functionalization and exploration of new chemical reactions and pathways.
Used in Materials Science:
In the field of materials science, 2,3,4-Furantricarboxylic acid, 5-(dimethylamino)-, trimethyl ester (9CI) has been studied for its potential use in the development of new materials with specific properties. Its incorporation into polymers or other materials could lead to advancements in areas such as electronics, coatings, or sensors.
Used in Medicinal and Therapeutic Formulations:
2,3,4-Furantricarboxylic acid, 5-(dimethylamino)-, trimethyl ester (9CI) has been investigated for its potential biological activity and use in medicinal and therapeutic formulations. Its unique structure and functional groups may contribute to the development of new treatments for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 191085-54-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,0,8 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 191085-54:
(8*1)+(7*9)+(6*1)+(5*0)+(4*8)+(3*5)+(2*5)+(1*4)=138
138 % 10 = 8
So 191085-54-8 is a valid CAS Registry Number.

191085-54-8Downstream Products

191085-54-8Relevant academic research and scientific papers

Rhodium(II)-catalyzed equilibration of push-pull carbonyl and ammonium ylides. A computationally based understanding of the reaction pathway

Padwa, Albert,Snyder, James P.,Curtis, Erin A.,Sheehan, Scott M.,Worsencroft, Kimberly J.,Kappe, C. Oliver

, p. 8155 - 8167 (2007/10/03)

Δ-Diazo esters containing an amido group in the γ-position have been found to undergo a rhodium(II)-catalyzed transformation, producing five-membered ammonium or carbonyl ylides depending on the reaction conditions used. In the absence of an external dipo

Ammonium ylide versus carbonyl ylide formation in the Rhodium(II)-catalyzed decomposition of diazoacetylureas. Generation and X-ray structure of a stable five-membered N-acyl ammonium ylide

Kappe, C. Oliver

, p. 3323 - 3326 (2007/10/03)

The Rh(II)-catalyzed decomposition of diazoacetylurea 5 gives rise to carbenoid intermediate 7 which can either cyclize to ammonium ylide 6 or to the isomeric carbonyl ylide dipole 8. In the presence or a rhodium catalyst, ammonium ylide 6 rearranges to c

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