5720-26-3 Usage
Uses
Used in Chemical Synthesis:
5-HYDROXYDOPAMINE HYDROCHLORIDE is used as a precursor for the preparation of hydrogen peroxide, superoxide radical, and hydroxyl radical. Its role in these processes is crucial for various chemical reactions and research studies.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-HYDROXYDOPAMINE HYDROCHLORIDE is used as an intermediate in the synthesis of various drugs and medications. Its chemical properties make it a valuable component in the development of new pharmaceutical compounds.
Used in Research and Development:
5-HYDROXYDOPAMINE HYDROCHLORIDE is employed as a research compound in the field of neuroscience, particularly in studying the effects of dopamine and its role in the central nervous system. It is also used in the investigation of oxidative stress and its implications in various diseases.
Used in Analytical Chemistry:
5-HYDROXYDOPAMINE HYDROCHLORIDE is utilized as an analytical reagent in the detection and quantification of specific substances in chemical analysis. Its unique properties make it suitable for use in various analytical techniques.
Used in Environmental Science:
In environmental science, 5-HYDROXYDOPAMINE HYDROCHLORIDE is used in the study of pollutant degradation and the effects of environmental stressors on ecosystems. Its role in these studies helps to understand the impact of pollutants and develop strategies for environmental protection.
Check Digit Verification of cas no
The CAS Registry Mumber 5720-26-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,2 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5720-26:
(6*5)+(5*7)+(4*2)+(3*0)+(2*2)+(1*6)=83
83 % 10 = 3
So 5720-26-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO3/c9-2-1-5-3-6(10)8(12)7(11)4-5/h3-4,10-12H,1-2,9H2/p+1
5720-26-3Relevant academic research and scientific papers
Biosynthesis. Part 24. Speculative Incorporation Experiments with 1-Benzylisoquinolines and a Logical Approach via C6-C2 and C6-C3 Precursors to the Biosynthesis of Hasubanonine and Protostephanine
Battersby, Alan R.,Jones, Raymond C. F.,Kazlauskas, Rymantas,Thornber, Craig W.,Ruchirawat, Somsak,Staunton, James
, p. 2016 - 2029 (2007/10/02)
Many possible 1-benzyltetrahydroisoquinolines have been examined as possible advanced precursors of the alkaloids hasubanonine (1) and protostephanine (2) in Stephania japonica plants, but none was incorporated significantly.Administration of various precursor molecules having only one aromatic ring, such as tyrosine, has demonstrated that both alkaloids are derived from two different C6-C2 biogenetic units.The subsequent failure of further 1-benzyltetrahydroisoquinolines and bisphenethylamines to be incorporated suggested the intermediacy of either (a) modified 1-benzylisoquinolines or (b) trioxygenated C6-C2 building blocks.Precursors designed to examine the first possibility, such as 1-benzyl-3,4-dihydroisoquinolines or 1-benzyl-1-carboxytetrahydroisoquinolines, were not incorporated into (1) and (2) whereas two 3',4',5'-trioxygenated 2-phenylethylamines were incorporated.These findings allow further delineation of the requirements for later precursors of the alkaloids (1) and (2).
