256407-56-4 Usage
Classification
Methyl ester derivative of 1H-pyrido[3,4-b]indole-1-acetic acid
Derived from a compound belonging to the indole class of chemicals.
Type
Synthetic organic molecule
Artificially created and not found naturally in the environment.
Potential applications
Pharmaceutical
May have potential use in the development of drugs and medications.
Structure
1H-pyrido[3,4-b]indole core
The central structure of the compound, which is based on the pyrido[3,4-b]indole framework.
Functional groups
Acetic acid and dimethylethoxy carbonyl
The functional groups attached to the core structure, which contribute to the compound's properties and reactivity.
Biological and pharmacological properties
Potential candidate for drug development and research
The compound may exhibit properties that could be useful in the treatment or management of diseases and conditions. Further research is needed to confirm these potential properties and their applications.
Check Digit Verification of cas no
The CAS Registry Mumber 256407-56-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,4,0 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 256407-56:
(8*2)+(7*5)+(6*6)+(5*4)+(4*0)+(3*7)+(2*5)+(1*6)=144
144 % 10 = 4
So 256407-56-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H24N2O4/c1-19(2,3)25-18(23)21-10-9-13-12-7-5-6-8-14(12)20-17(13)15(21)11-16(22)24-4/h5-8,15,20H,9-11H2,1-4H3
256407-56-4Relevant academic research and scientific papers
Palladium-catalyzed heteroannulation approach to 1,2-bis(3-indolyl)ethanes
Blair, Lachlan M.,Sperry, Jonathan
supporting information, p. 1931 - 1936 (2013/09/24)
Palladium-catalyzed heteroannulation between indole-3-butanal and various o-iodoanilines provides a straightforward synthesis of 1,2-bis(3-indolyl) ethanes, which are useful precursors to valued indolo[2,3a]carbazoles. 1,2-Bis(3-indolyl)ethanes bearing a
Synthetic study towards strictamine: The oxidative coupling approach
Ren, Weiwu,Tappin, Nicholas,Wang, Qian,Zhu, Jieping
supporting information, p. 1941 - 1944 (2013/09/24)
A synthetic approach featuring a key intramolecular oxidative coupling of a dianion for the formation of the C7-C16 bond was exploited aiming at the synthesis of strictamine. Treatment of substituted tetrahydrocarboline with LHMDS at -78 °C followed by iodine at room temperature afforded a tetracyclic compound, a substructure of eburnane-type alkaloid, via the formation of the Na-C16 bond.
Synthesis of ajmalicine derivatives using Wittig-Horner and Knoevenagel reactions
Boumendjel, Ahcene,Nuzillard, Jean-Marc,Massiot, Georges
, p. 9033 - 9036 (2007/10/03)
2-(2,3,4,9-Tetrahydro-1H-β-carbolin-1-yl)acetaldehyde, synthesized from tryptamine in five steps, is easily homologated by Wittig-Horner or Knoevenagel reactions to substituted acrylates. These highly reactive compounds are key intermediates in the synthesis of analogs of the natural indol alkaloid ajmalicine.
