74054-32-3 Usage
General Description
2,3-Dihydro-5,6-dimethoxy-1-(methoxycarbonyl)-1H-indole is a chemical compound with the molecular formula C14H17NO4. It is a derivative of the indole class of organic compounds, which are commonly found in various natural sources such as plants and fungi. This particular compound is characterized by its two methoxy groups and a methoxycarbonyl group attached to the indole ring, giving it unique properties and potential applications in the field of medicinal chemistry. It may have potential use in pharmaceutical research due to its structural features, which could contribute to its biological activity and potential therapeutic effects. Additionally, it may also have potential applications in other fields such as material science or organic synthesis. Overall, 2,3-Dihydro-5,6-dimethoxy-1-(methoxycarbonyl)-1H-indole presents an interesting and potentially valuable compound for further study and exploration.
Check Digit Verification of cas no
The CAS Registry Mumber 74054-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,0,5 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74054-32:
(7*7)+(6*4)+(5*0)+(4*5)+(3*4)+(2*3)+(1*2)=113
113 % 10 = 3
So 74054-32-3 is a valid CAS Registry Number.
74054-32-3Relevant academic research and scientific papers
Studies on the Syntheses of Heterocyclic Compounds. Part 865. A Novel Synthesis of Indole Derivatives by Intramolecular Nucleophilic Aromatic Substitution
Kametani, Tetsuji,Ohsawa, Tatsushi,Ihara, Masataka
, p. 290 - 294 (2007/10/02)
Cyclisation of N-(2-bromo-4,5-dimethoxyphenethyl)acetamide (6) afforded 1-acetyl-2,3-dihydro-5,6-dimethoxy-1H-indole (13) by intramolecular nucleophilic aromatic substitution using sodium hydride and cuprous halide in dimethylformamide.The dihydroindoles (14), (15), and (16) were also synthesised from the corresponding amides (8) and (10) and the carbamate (12) in a similar manner.The dihydroindoles (13), (14), and (16) were converted into the indoles (20) and (21) in excellent yield by oxidation and subsequent alkaline hydrolysis.The 2-oxindoles (26) and (27) were also prepared under similar reaction condition from the phenylacetamide (24) and (25).
A NOVEL SYNTHESIS OF INDOLE DERIVATIVES
Kametani, Tetsuji,Ohsawa, Tatsushi,Ihara, Masataka
, p. 277 - 280 (2007/10/02)
1-Acetyl-2,3-dihydro-5,6-dimethoxy-1H-indole (13) was synthesized by cyclization of N-(2-bromo-4,5-dimethoxyphenethyl)acetamide (6) using sodium hydride and cuprous halide in dimethylformamide.Indoles (14,15 and 16) were prepared in a similar manner from
