749864-17-3 Usage
Description
(R)-2-[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-amino-3-(1H-indol-3-yl)-propionic acid methyl ester is a complex organic compound that features a combination of benzo[1,3]dioxol, indole, propionic acid, and methyl ester functional groups. This derivative of propionic acid includes a methyl ester group, an amino group connected to a benzo[1,3]dioxol-5-yl-meth-(E)-ylidene, and an indole group. Its stereochemistry is classified as (R), which may influence its interactions with biological systems.
Uses
Used in Pharmaceutical and Medicinal Research:
(R)-2-[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-amino-3-(1H-indol-3-yl)-propionic acid methyl ester is used as a compound with potential applications in pharmaceutical and medicinal research. The presence of indole and benzo[1,3]dioxol-5yl-meth-(E)-ylidene groups suggests that this compound may have biological activities and the ability to interact with biological systems. Further research is necessary to fully understand its potential uses and effects.
Used in Chemical Synthesis:
(R)-2-[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-amino-3-(1H-indol-3-yl)-propionic acid methyl ester can be used as a building block or intermediate in the synthesis of more complex molecules for various applications, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and functional groups make it a valuable candidate for creating novel compounds with specific properties and functions.
Used in Material Science:
(R)-2-[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-amino-3-(1H-indol-3-yl)-propionic acid methyl ester may also find applications in material science, particularly in the development of new materials with unique properties. The combination of benzo[1,3]dioxol, indole, and propionic acid groups could potentially lead to the creation of materials with specific optical, electronic, or mechanical characteristics, depending on the compound's behavior in different environments and its interactions with other molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 749864-17-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,9,8,6 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 749864-17:
(8*7)+(7*4)+(6*9)+(5*8)+(4*6)+(3*4)+(2*1)+(1*7)=223
223 % 10 = 3
So 749864-17-3 is a valid CAS Registry Number.
749864-17-3Relevant articles and documents
Improved synthesis of tadalafil using dimethyl carbonate and ionic liquids
Earle, Martyn J.,Noe, Marco,Perosa, Alvise,Seddon, Kenneth R.
, p. 1204 - 1211 (2014)
An improved synthesis of tadalafil, a drug for the treatment of male erectile dysfunction, involves the use of safer solvents and reagents as well as a reduced number of steps.
