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1H-Pyrrole-2-carboxylic acid, 4-ethyl-3-methyl-5-[[3-methyl-5-[(phenylmethoxy)carbonyl]-1H-pyrrol-2-yl]methyl]-, 1,1-dimethylethyl ester is a complex organic compound with a molecular formula of C23H27NO4. It is a derivative of pyrrole-2-carboxylic acid, featuring a 4-ethyl-3-methyl-5-alkyl substituent with a 3-methyl-5-[(phenylmethoxy)carbonyl]-1H-pyrrol-2-yl group attached to the alkyl chain. The compound also has a 1,1-dimethylethyl ester group, which is a tert-butyl ester. This molecule is characterized by its unique structure, which includes a pyrrole ring, an ester group, and various alkyl and aryl substituents. It is likely to be found in the field of organic chemistry, potentially as an intermediate in the synthesis of pharmaceuticals or other complex organic molecules.

97346-03-7

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97346-03-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97346-03-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,4 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97346-03:
(7*9)+(6*7)+(5*3)+(4*4)+(3*6)+(2*0)+(1*3)=157
157 % 10 = 7
So 97346-03-7 is a valid CAS Registry Number.

97346-03-7Downstream Products

97346-03-7Relevant academic research and scientific papers

TOTAL SYNTHESES OF NEW PORPHYRINS ISOLATED FROM THE CORAL SEA DEMOSPONGE CORALLISTES SP.

Pandey, Ravindra K.,Leung, Sam H.,Smith, Kevin M.

, p. 8093 - 8096 (2007/10/02)

Three new metal-free porphyrins, corallistin B, corallistin C and corallistin E isolated from the demosponge Corallistes sp. were synthesized as methyl esters in excellent yield by using either the MacDonald or a,c-biladiene routes to porphyrins.

Reactions on solid supports part II: a convenient method for synthesis of pyrromethanes using a montmorillonite clay as catalyst

Jackson, Anthony H.,Pandey, Ravindra K.,Nagaraja Rao,Roberts, Edward

, p. 793 - 796 (2007/10/02)

α-Acetoxymethylpyrroles couple with α-free pyrroles in presence of Montmorillonite clay to form unsymmetrical pyrromethanes in excellent yields. Symmetrical pyrromethanes were also prepared in a similar manner by clay catalysed self-condensation of α-acet

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