73083-07-5 Usage
Molecular structure
The compound has an isoquinoline ring with a carboxylic acid functional group and an ethyl ester moiety attached to it. It also contains a 4-bromophenyl group and two methoxy groups.
Molecular weight
390.26 g/mol
Appearance
The compound is not described in the material provided, so its appearance is unknown.
Solubility
The compound's solubility is not described in the material provided.
Biological activity
The compound has potential applications in the pharmaceutical industry due to its structural features, which may contribute to biological activity.
Synthesis
The synthesis of the compound is not described in the material provided.
Properties
The properties of the compound, such as its melting point, boiling point, and stability, are not described in the material provided.
Research and development
The compound is a valuable target for research and development in medicinal chemistry and drug discovery due to its synthesis and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 73083-07-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,8 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 73083-07:
(7*7)+(6*3)+(5*0)+(4*8)+(3*3)+(2*0)+(1*7)=115
115 % 10 = 5
So 73083-07-5 is a valid CAS Registry Number.
73083-07-5Relevant articles and documents
One-pot α-amidosulfone-mediated variation of the pictet-Spengler tetrahydroisoquinoline synthesis, suitable for amide-type substrates
Arroyo, Francisco J.,López-Alvarado, Pilar,Ganesan,Menéndez, J. Carlos
, p. 5720 - 5727 (2014/11/07)
The development of Pictet-Spengler reactions from amide substrates is a challenging problem. We report here that the reaction between amide-type compounds (including carbamates, amides, ureas and diketopiperazines), aldehydes and p-toluenesulfinic acid constitutes an efficient method for the preparation of tetrahydroisoquinolines or pyrazino-[2,1-b]isoquinolines. Unlike previously known methods, this one-pot Pictet-Spengler protocol avoids the need for strong Lewis or Br?nsted acid catalysts.
