70494-48-3 Usage
Description
(S)-3,4-DIMETHOXYPHENYLALANINE METHYL ESTER HYDROCHLORIDE is a chemical compound that features an amino acid derivative and a methyl ester group. It is widely utilized in organic synthesis and pharmaceutical research due to its potential applications in the development of new drugs and as a building block in the synthesis of complex organic molecules. Furthermore, it may possess biological activity, making it a valuable compound for studying various biochemical processes. The hydrochloride form of the compound enhances its stability and solubility in water.
Uses
Used in Pharmaceutical Research:
(S)-3,4-DIMETHOXYPHENYLALANINE METHYL ESTER HYDROCHLORIDE is used as a key intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its unique structure allows for the development of novel drugs with potential therapeutic benefits.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-3,4-DIMETHOXYPHENYLALANINE METHYL ESTER HYDROCHLORIDE serves as a valuable building block for the creation of complex organic molecules. It is used as a starting material or a reagent in [application reason], enabling the synthesis of a wide range of compounds with diverse applications.
Used in Biochemical Research:
(S)-3,4-DIMETHOXYPHENYLALANINE METHYL ESTER HYDROCHLORIDE is employed as a research tool in the study of various biochemical processes. It is used as a probe or a substrate in [application reason], providing insights into the mechanisms of biological reactions and the development of targeted therapies.
Used in Drug Development:
(S)-3,4-DIMETHOXYPHENYLALANINE METHYL ESTER HYDROCHLORIDE is utilized as a potential drug candidate in the development of new therapeutic agents. It is used as a lead compound in [application reason], with the aim of identifying novel treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 70494-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,9 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70494-48:
(7*7)+(6*0)+(5*4)+(4*9)+(3*4)+(2*4)+(1*8)=133
133 % 10 = 3
So 70494-48-3 is a valid CAS Registry Number.
70494-48-3Relevant articles and documents
Substituted Dihydroisoquinolinones by Iodide-Promoted Cyclocarbonylation of Aromatic α-Amino Acids
Amer, Mostafa M.,Carrasco, Ana C.,Leonard, Daniel J.,Ward, John W.,Clayden, Jonathan
supporting information, p. 7977 - 7981 (2019/01/04)
Imidazolidinone derivatives of a range of aromatic α-amino acids, on treatment with phosgene and potassium iodide, undergo a mild Bischler-Napieralski-style cyclocarbonylation reaction that generates a tricyclic lactam by insertion of a C=O group between amino acid nitrogen and the ortho position of the aryl substituent. Regio- and diastereoselective functionalization of the lactam generates a library of substituted dihydroisoquinolinones and their congeners in enantioenriched form.
