881674-85-7 Usage
Molecular Weight
295.37 g/mol The molecular weight is the mass of one mole of the compound, calculated by adding the atomic weights of all the atoms in the molecular formula.
Structure
1H-Pyrrole-3-carboxylic acid, 2-methyl-1-(phenylsulfonyl)-, ethyl ester The structure of the compound is a pyrrole ring with a carboxylic acid group attached to the 3-position, a methyl group attached to the 2-position, a phenylsulfonyl group attached to the 1-position, and an ethyl ester group attached to the carboxylic acid.
Class
Pyrrole derivatives The compound belongs to the class of pyrrole derivatives, which are organic compounds that contain a pyrrole ring.
Applications
Organic synthesis, pharmaceuticals, materials science The compound has potential applications in the field of organic synthesis as a building block for the synthesis of various organic compounds. It may also exhibit biological activity that could be of interest for pharmaceutical research. Additionally, it may have potential uses in materials science.
Further Research Needed
More research and testing are needed to fully understand the potential uses and applications of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 881674-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,6,7 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 881674-85:
(8*8)+(7*8)+(6*1)+(5*6)+(4*7)+(3*4)+(2*8)+(1*5)=217
217 % 10 = 7
So 881674-85-7 is a valid CAS Registry Number.
881674-85-7Relevant articles and documents
Development and Scope of the Arene-Fused Domino Michael/Mannich Reaction: Application to the Total Syntheses of Aspidosperma Alkaloids (-)-Aspidospermidine, (-)-Tabersonine, and (-)-Vincadifformine
Zhao, Senzhi,Andrade, Rodrigo B.
, p. 521 - 531 (2017/04/26)
The development and application of the arene-fused domino Michael/Mannich route to the tetrahydrocarbazole (ABE) core of Aspidosperma alkaloids is described. The scope of this novel transformation was studied in terms of the nucleophilic component (i.e., N-sulfinyl metallodienamine) and the electrophilic component (i.e., Michael acceptor). The successful application of this methodology toward the concise total syntheses of classical indole alkaloids (-)-aspidospermidine, (-)-tabersonine, and (-)-vincadifformine in 10-11 steps, respectively, is also discussed.
INHIBITORS OF THE HIV INTEGRASE ENZYME
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Page/Page column 55, (2010/11/27)
The present invention is directed to compounds of formula (I), and pharmaceutically acceptable salts and solvates thereof, their synthesis, and their use as modulators or inhibitors of the human immunodeficiency virus (“HIV”) integrase enzyme.
