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1H-Pyrrole-3-carboxylic acid, 1-methyl-2-phenyl, methyl ester is a complex organic compound with the chemical formula C13H13NO2. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with four carbon atoms and one nitrogen atom. In this specific compound, the pyrrole ring is substituted with a carboxylic acid group at the 3-position, a methyl group at the 1-position, and a phenyl group at the 2-position. The carboxylic acid group is further esterified with a methyl group, resulting in a methyl ester. 1H-Pyrrole-3-carboxylic acid, 1-methyl-2-phenyl-, 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.

91003-38-2

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91003-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91003-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,0 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91003-38:
(7*9)+(6*1)+(5*0)+(4*0)+(3*3)+(2*3)+(1*8)=92
92 % 10 = 2
So 91003-38-2 is a valid CAS Registry Number.

91003-38-2Downstream Products

91003-38-2Relevant academic research and scientific papers

α',α'-DISILYLATED TERTIARY BENZAMIDES AS DUAL ORTHO- AND α'-CARBANION SYNTHONS. AMIDE PETERSON OLEFINATION ROUTES TO N-BENZOYL ENAMINES, ISOQUINOLINES, AND DIBENZAZOCINES

Cuevas, J.-C.,Patil, P.,Snieckus, V.

, p. 5841 - 5844 (2007/10/02)

α',α'-Disilylated benzamides 2, prepared by LiTMP/TMSCl in situ trap procedure, constitute ortho- and α'-carbanion synthons which provide N-benzoyl enamines (5), isoquinolines (6), dibenzoazocines (9) by Peterson olefination, and pyrroles (11) by cycloaddition.The conversion of 2 into other useful functionality is described.

Generation of Azomethine Ylides via the Desilylation Reaction of Immonium Salts

Padwa, Albert,Haffmanns, Gunter,Tomas, Miguel

, p. 3314 - 3322 (2007/10/02)

Generation of intermediates having azomethine ylide reactivity was achieved by the reaction of several ethanol or thioimidate derivatives with methyl iodide followed by treatment of the resulting imine with (trimethylsilyl)methyl triflate.Desilylation of

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