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(-)-Methyl 2-benzyl-3-methoxycarbonyl-9-methyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-1-propionate is a complex organic compound with a molecular formula of C26H28N2O4. It is a derivative of the pyridoindole class of alkaloids, characterized by a pyridoindole core structure with various substituents. (-)-methyl 2-benzyl-3-methoxycarbonyl-9-methyl-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole-1-propionate features a methyl group at the 1-position, a benzyl group at the 2-position, a methoxycarbonyl group at the 3-position, and a 9-methyl group. The compound is also a 1,2,3,4-tetrahydro derivative, indicating the presence of four hydrogen atoms in the molecule. It is a propionate ester, which means it has a propionic acid group esterified to the molecule. (-)-methyl 2-benzyl-3-methoxycarbonyl-9-methyl-1,2,3,4-tetrahydro-9H-pyrido<3,4-b>indole-1-propionate has potential applications in pharmaceutical research due to its unique structure and properties, and it may be involved in the synthesis of various biologically active compounds.

4837-57-4

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4837-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4837-57-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,3 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4837-57:
(6*4)+(5*8)+(4*3)+(3*7)+(2*5)+(1*7)=114
114 % 10 = 4
So 4837-57-4 is a valid CAS Registry Number.

4837-57-4Relevant academic research and scientific papers

Pictet-Spengler reactions in aprotic media. The total synthesis of (±) suaveoline

Trudell,Soerens,Weber,Hutchins,Grubisha,Bennett,Cook

, p. 1805 - 1822 (2007/10/02)

The first total synthesis of the indole alkaloid (±)-suaveoline 1 (a macroline-related base and a member of the sarpagine/ajmaline class of alkaloids) was completed in a stereocontrolled fashion. The serial synthesis employed three intramolecular reaction

Stereochemistry of Methyl 2-Benzyl-3-methoxycarbonyl-9-methyl-1,2,3,4-tetrahydro-9H-pyridoindole-1-propionate

Shimizu, Masato,Ishikawa, Masayuki,Komoda, Yasuo,Nakajima, Terumi,Yamaguchi, Keiichi,Yoneda, Naoto

, p. 463 - 474 (2007/10/02)

The Pictet-Spengler reaction of Na-methyl-Nb-benzyltryptophan methyl ester hydrochloride (4a) with methyl 3-formylpropionate was carried out in 50percent aqueous MeOH under reflux to afford methyl trans-2-benzyl-3-methoxycarbonyl-9-m

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