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1H-Pyrrole-2-carboxylic acid, 5,5'-methylenebis[4-(2-chloroethyl)-3-methyl-, bis(phenylmethyl) ester is a complex organic compound with the chemical formula C34H34Cl2N2O4. It is a derivative of pyrrole-2-carboxylic acid, featuring a bis(phenylmethyl) ester group and two 4-(2-chloroethyl)-3-methyl substituents connected by a methylene bridge. 1H-Pyrrole-2-carboxylic acid, 5,5'-methylenebis[4-(2-chloroethyl)-3-methyl-, bis(phenylmethyl) ester is characterized by its unique structure, which includes a pyrrole ring, a carboxylic acid group, and a bis(phenylmethyl) ester functionality. The presence of chlorine atoms in the molecule contributes to its reactivity and potential applications in various chemical processes. Due to its complexity, 1H-Pyrrole-2-carboxylic acid, 5,5'-methylenebis[4-(2-chloroethyl)-3-methyl-, bis(phenylmethyl) ester is likely to be used in specialized fields such as pharmaceuticals, agrochemicals, or as an intermediate in the synthesis of other complex organic molecules.

63089-18-9

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63089-18-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63089-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,8 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63089-18:
(7*6)+(6*3)+(5*0)+(4*8)+(3*9)+(2*1)+(1*8)=129
129 % 10 = 9
So 63089-18-9 is a valid CAS Registry Number.

63089-18-9Downstream Products

63089-18-9Relevant academic research and scientific papers

Long Wavelength Photosensitizers Related to Chlorins and Bacterioclorins for use in Photodynamic Therapy

Pandey, Ravindra K.,Shiau, Fuu-Yau,Ramachandran, Kishore,Dougherty, Thomas J.,Smith, Kevin M.

, p. 1377 - 1386 (2007/10/02)

A series of long wavelength photosensitizers related to chlorins and bacteriochlorins has been synthesized from the Diels-Alder reaction of protoporphyrin III dimethyl ester 6, or protoporphyrin II dimethyl ester 29.These porphyrins were prepared either b

Synthetic and Biosynthetic Studies of Porphyrins.Part10.Syntheses of Porphyrins with Acetic,Propionic,and Butyric Acid Side-chains for Biosynthetic Syudies.

Jackson, Anthony H.,Pandey, Ravindra K.,Smith, Kevin M.

, p. 299 - 306 (2007/10/02)

In connection with studies of substrate specificity of uroporphyrinogen decarboxylase and coproporphyrinogen oxidase, enzymes in the heme and chlorophyll biosynthetic pathways,and heme oxygenase,an enzyme involved in the catabolism of hemes,we have synthesized a number of new porphyrins substituted with acetic,propionic,and butyric side-chains,using the a,c-biladiene route;one porphyrin was also prepared by the MacDonald pyrromethane approach.In one of the a,c-biladiene cyclizations,meso-chlorinated porphyrins were formed as minor by products,but this side-reaction was suppressed by carefully drying the copper(II) chloride used in this stage, or by use of copper(II) acetate as an alternative oxidant.

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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