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1H-Pyrrole-3-carboxylic acid, 4-(3-methoxyphenyl)-2,5-dimethyl, methyl ester is a complex organic compound with the molecular formula C14H17NO3. It is a derivative of pyrrole, a heterocyclic aromatic organic compound containing a five-membered ring with one nitrogen atom and four carbon atoms. In this specific compound, the pyrrole ring is substituted with a carboxylic acid group at the 3-position, a methyl group at the 2-position, and a 3-methoxyphenyl group at the 4-position. The 5-position is also occupied by a methyl group. The carboxylic acid group is further esterified with a methyl group, making it a methyl ester. 1H-Pyrrole-3-carboxylic acid, 4-(3-methoxyphenyl)-2,5-dimethyl-, methyl ester is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in the development of new materials with unique properties.

95838-61-2

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95838-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95838-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,8,3 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95838-61:
(7*9)+(6*5)+(5*8)+(4*3)+(3*8)+(2*6)+(1*1)=182
182 % 10 = 2
So 95838-61-2 is a valid CAS Registry Number.

95838-61-2Downstream Products

95838-61-2Relevant academic research and scientific papers

One-pot three-component synthesis of tetrasubstituted N - H pyrroles from secondary propargylic alcohols, 1,3-dicarbonyl compounds and tert-butyl carbamate

Cadierno, Victorio,Gimeno, Jose,Nebra, Noel

experimental part, p. 233 - 236 (2010/04/27)

(Chemical Equation Presented) Several tetrasubstituted N - H pyrroles, functionalized with ester or ketone groups at C-3 position, were prepared by one-pot coupling of secondary propargylic alcohols with 1,3-dicarbonyl compounds and tert-butyl carbamate,

Heterocycles from α-Nitroolefins, VIII. - 2-Methyl-3-pyrrolecarboxylates from α-Nitroolefins and Acetoacetates

Boberg, Friedrich,Garburg, Karl-Heinz,Goerlich, Karl-Joachim,Pipereit, Eberhard,Ruhr, Maria

, p. 239 - 250 (2007/10/02)

3-Pyrrolecarboxylates 4 can be prepared from α-nitroolefins 1 and acetoacetates 2 by two methods: (a) 1 and 2 react to give 4,5-dihydro-5-methyleneamino-3-furancarboxylates 3 which are hydrolyzed, (b) the nitronic acids 8, adducts of 1 and 2, yield with different reduction agents the heterocycles 4.

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