27347-13-3 Usage
Description
4-(2-methoxyphenyl)morpholine is a morpholine derivative with the molecular formula C11H15NO2, featuring a heterocyclic organic compound structure that includes both nitrogen and oxygen atoms in its ring.
Usage:
Used in Organic Synthesis:
4-(2-methoxyphenyl)morpholine is used as a building block in organic synthesis for creating a variety of complex organic molecules, leveraging its unique structural properties to facilitate chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(2-methoxyphenyl)morpholine is utilized as an intermediate for the synthesis of various drugs, contributing to the development of new medicinal compounds.
Used as a Corrosion Inhibitor:
4-(2-methoxyphenyl)morpholine has been studied for its potential use as a corrosion inhibitor, indicating its ability to protect materials from degradation in various industrial applications.
Used as an Anti-inflammatory Agent:
4-(2-methoxyphenyl)morpholine has also been investigated for its anti-inflammatory properties, suggesting a possible role in the development of treatments for inflammatory conditions.
Used in Neuroscience Research:
4-(2-methoxyphenyl)morpholine has shown promise in biological research, particularly in neuroscience, due to its capacity to modulate certain neurotransmitter systems, which could be instrumental in understanding and treating neurological disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 27347-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,4 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 27347-13:
(7*2)+(6*7)+(5*3)+(4*4)+(3*7)+(2*1)+(1*3)=113
113 % 10 = 3
So 27347-13-3 is a valid CAS Registry Number.
27347-13-3Relevant articles and documents
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Sineokov et al.
, (1970)
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Aerobic iron-catalyzed site-selective C(sp3)–C(sp3) bond cleavage in N-heterocycles
Beller, Matthias,Junge, Kathrin,Leonard, David K.,Li, Wu,Rockstroh, Nils
, (2021/06/26)
The kinetic and thermodynamic stability of C(sp3)–C(sp3) bonds makes the site-selective activation of these motifs a real synthetic challenge. In view of this, herein a site-selective method of C(sp3)–C(sp3) bon
Aryl-Diadamantyl Phosphine Ligands in Palladium-Catalyzed Cross-Coupling Reactions: Synthesis, Structural Analysis, and Application
Sinai, ádám,Simkó, Dániel Cs.,Szabó, Fruzsina,Paczal, Attila,Gáti, Tamás,Bényei, Attila,Novák, Zoltán,Kotschy, András
supporting information, p. 1122 - 1128 (2020/03/03)
Synthesis, temperature-dependent NMR structure investigation and utilization of a new, stable and easily accessible aryl-diadamantylphosphine ligand family is reported. The bulky and electron-rich phosphorus center of the ligand enhances the catalytic activity of palladium in cross-coupling reactions of sterically demanding ortho-substituted aryl halides. In our study, we demonstrated the synthetic applicability of the new phosphine ligands in Buchwald-Hartwig and tosyl hydrazone coupling reactions.
