55-59-4 Usage
Uses
Used in Pharmaceutical Industry:
(S)-2-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID is used as an intermediate in the synthesis of various pharmaceutical compounds, particularly those with potential neurological or psychiatric applications. Its unique structure and chirality make it a valuable building block for the development of new drugs targeting specific receptors or enzymes in the central nervous system.
Used in Chemical Synthesis:
(S)-2-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID is used as a starting material in the synthesis of peptide-based metal ion sensors. Its incorporation into peptide sequences allows for the development of sensors with high selectivity and sensitivity for detecting specific metal ions, which can be useful in environmental monitoring, medical diagnostics, and other analytical applications.
Used in Research and Development:
(S)-2-AMINO-3-(3,4-DIMETHOXY-PHENYL)-PROPIONIC ACID is also used as a research tool in the study of enzyme mechanisms, receptor binding, and other biological processes. Its unique structure and chirality make it an interesting probe for investigating the stereoselectivity of enzymes and the role of chirality in molecular recognition.
Check Digit Verification of cas no
The CAS Registry Mumber 55-59-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55-59:
(4*5)+(3*5)+(2*5)+(1*9)=54
54 % 10 = 4
So 55-59-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO4/c1-15-9-4-3-7(6-10(9)16-2)5-8(12)11(13)14/h3-4,6,8H,5,12H2,1-2H3,(H,13,14)/t8-/m0/s1
55-59-4Relevant academic research and scientific papers
Bio-inspired enantioselective full transamination using readily available cyclodextrin
Zhang, Shiqi,Li, Guangxun,Liu, Hongxin,Wang, Yingwei,Cao, Yuan,Zhao, Gang,Tang, Zhuo
, p. 4203 - 4208 (2017/02/05)
The mimics of vitamin B6-dependent enzymes that catalyzed an enantioselective full transamination in the pure aqueous phase have been realized for the first time through the establishment of a new “pyridoxal 5′-phosphate (PLP) catalyzed non-covalent cyclodextrin (CD)-keto acid inclusion complexes” system, and various optically active amino acids have been obtained.
Levodopa methyl ester hydrochloride synthetic method
-
, (2017/09/01)
The invention relates to a synthesis method of L-dopa methyl ester hydrochloride, which comprises the following steps: by using veratone as a raw material, carrying out amidation to obtain 2-amino-3-(3,4-dimethoxyphenyl)propanamide, carrying out amide oxidation into carboxy group to obtain 2-amino-3-(3,4-dimethoxyphenyl)propionic acid, removing methoxy group to obtain 2-amino-3-(3,4-dihydroxyphenyl)propionic acid, and finally, carrying out methyl ester conversion and acidification to obtain the target product 2-amino-3-(3,4-dimethoxyphenyl)alanine methyl ester hydrochloric acid. The method has the advantages of accessible reaction raw materials, ingenious technique concept, simple steps and no use of virulent reagents, is simple to operate, conforms to the requirements for green chemical industry, and is suitable for industrial production.
