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1H-Pyrrole-3-acetic acid, 4-formyl-5-methyl-2-[(phenylmethoxy)carbonyl]-, phenylmethyl ester is a complex organic compound with a molecular formula of C21H19NO5. It is a derivative of 1H-pyrrole-3-acetic acid, featuring a 4-formyl-5-methyl-2-[(phenylmethoxy)carbonyl] group attached to the pyrrole ring. The phenylmethyl ester functional is group present, indicating an ester linkage between the phenylmethyl moiety and the carboxylic acid group. 1H-Pyrrole-3-acetic acid, 4-formyl-5-methyl-2-[(phenylmethoxy)carbonyl]-, phenylmethyl ester is characterized by its unique structure, which includes a pyrrole ring, a formyl group, a methyl group, a phenylmethoxycarbonyl group, and a phenylmethyl ester group. It is likely to be found in research settings, particularly in the fields of organic chemistry and medicinal chemistry, where such complex structures are studied for their potential applications in drug development or as intermediates in the synthesis of other compounds.

87308-15-4

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87308-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87308-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,3,0 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 87308-15:
(7*8)+(6*7)+(5*3)+(4*0)+(3*8)+(2*1)+(1*5)=144
144 % 10 = 4
So 87308-15-4 is a valid CAS Registry Number.

87308-15-4Relevant academic research and scientific papers

Methyl Deuteration Reactions in Vinylporphyrins: Protoporphyrins IX, III, and XIII

Smith, Kevin M.,Parish, Daniel W.,Inouye, Warren S.

, p. 666 - 671 (2007/10/02)

Base-catalyzed deuteration of the methyl groups in protoporphyrin IX dimethyl ester (1) proceeds with differential deuteration; rate of deuteration, as measured by NMR spectroscopy of reaction products, follows the order 3-Me > 1-Me >5-Me >8-Me.A simple q

Neighboring Group Participation in the Pyrrole Series

Smith, Kevin M.,Martynenko, Zoya,Pandey, Ravindra K.,Tabba, Hani D.

, p. 4296 - 4302 (2007/10/02)

With use of proton and carbon-13 NMR spectroscopy of deuterium- and carbon-13-labeled substrates, the transformation of certain (2-hydroxyethyl)pyrroles (4, 18, 21) into the corresponding (2-haloethyl)pyrroles (using thionyl chloride/pyridine or triphenyl

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