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1H-Pyrrole-3-acetic acid, 1-benzoyl-4-(3-ethoxy-3-oxo-1-propenyl)-2-formyl-, ethyl ester is a complex organic compound with the molecular formula C18H17NO5. It is a derivative of 1H-pyrrole-3-acetic acid, which is a heterocyclic compound containing a pyrrole ring and a carboxylic acid group. The compound features a benzoyl group attached to the pyrrole ring, and a 3-ethoxy-3-oxo-1-propenyl group connected to the formyl group. The ethyl ester functional group is present, indicating that the carboxylic acid group is esterified with ethanol. 1H-Pyrrole-3-acetic acid, 1-benzoyl-4-(3-ethoxy-3-oxo-1-propenyl)-2-formyl-, ethyl ester is likely to be found in the field of organic chemistry, potentially as an intermediate in the synthesis of pharmaceuticals or other complex molecules, due to its diverse functional groups and structural features.

91233-64-6

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91233-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91233-64-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,2,3 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 91233-64:
(7*9)+(6*1)+(5*2)+(4*3)+(3*3)+(2*6)+(1*4)=116
116 % 10 = 6
So 91233-64-6 is a valid CAS Registry Number.

91233-64-6Downstream Products

91233-64-6Relevant academic research and scientific papers

Pyrrole chemistry. XXVII. 2,3,4-Trisubstituted pyrroles and a second synthesis of porphobilinogen from pyrrole

Faber, Kurt,Anderson, Hugh J.,Loader, Charles E.,Daley, Annette S.

, p. 1046 - 1050 (2007/10/02)

Changes in some of the key intermediates and procedures used in our earlier total synthesis of porphobilinogen from pyrrole that improve the yield to 11percent are reported.Ethyl pyrrole-3-acetate was formylated by the Vilsmeier-Haack method and then iodi

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