91384-88-2 Usage
Uses
Used in Organic Synthesis:
3,4-DIMETHOXY[7-13C]-BENZYL ALCOHOL is used as a synthetic intermediate for the production of a range of organic compounds. Its unique structure, featuring a benzyl alcohol core with methoxy groups at the 3 and 4 positions, and a 13C-labeled carbon at the 7 position, makes it a versatile building block in the synthesis of complex organic molecules.
Used in Chemical Research:
In the realm of chemical research, 3,4-DIMETHOXY[7-13C]-BENZYL ALCOHOL is employed as a labeled compound to study the behavior of molecules in chemical reactions. The incorporation of 13C allows researchers to track the movement and transformation of the molecule during synthesis processes, providing valuable insights into reaction mechanisms and pathways.
Used in Pharmaceutical Industry:
3,4-DIMETHOXY[7-13C]-BENZYL ALCOHOL is also utilized in the pharmaceutical industry as a key component in the development of new drugs. Its unique properties and reactivity make it suitable for the synthesis of pharmaceutical agents, potentially leading to the discovery of novel therapeutics with improved efficacy and selectivity.
Used in Biochemical Studies:
In biochemical research, 3,4-DIMETHOXY[7-13C]-BENZYL ALCOHOL can be used as a labeled compound to investigate enzyme mechanisms, metabolic pathways, and the interactions between biomolecules. The 13C-labeling allows for the precise tracking of the molecule's behavior in biological systems, contributing to a deeper understanding of biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 91384-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,3,8 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91384-88:
(7*9)+(6*1)+(5*3)+(4*8)+(3*4)+(2*8)+(1*8)=152
152 % 10 = 2
So 91384-88-2 is a valid CAS Registry Number.
91384-88-2Relevant academic research and scientific papers
Synthesis of Dopamines Labelled with 13C in the α- or β-Side Chain Position and Their Application to Structural Studies on Melanins by Solid-State NMR Spectroscopy
Crescenzi, Orlando,Kroesche, Christoph,Hoffbauer, Wilfried,Jansen, Martin,Napolitano, Alessandra,et al.
, p. 563 - 568 (2007/10/02)
Solid-state NMR spectroscopy was applied to the analysis of melanins prepared by peroxidase-H2O2 oxidation of dopamines specifically 13C labelled in the α- or β-side chain positions.A surprisingly diverse pattern of signals indicated the presence of uncyclized dopamine and noradrenaline-derived units, in addition to indole and carbonyl carbon atoms.These structural features, coupled with the results obtained from elemental analysis of dopamine melanin samples prepared under different conditions, point to a pigment formation process more complex than previously believed. - Key Words: CP-MAS NMR Spectroscopy / Melanin / Oxidative phenolic coupling / Quinone methides / Labelled compounds, 13C / Dopamines / Enzymes
