Molecular structure of 2-Methoxybenzylamine, CAS Number: 6850-57-3
2-Methoxybenzylamine (CAS 6850-57-3)
CAS Number:
6850-57-3
Purity:
≥97%
Molecular Weight:
137.18
Molecular Formula:
C8H11NO
Supplemental Information:
This is as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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2-Methoxybenzylamine functions as a nucleophilic reagent in organic synthesis. It acts as a versatile building block in the preparation of various organic compounds, particularly in the formation of amine derivatives and heterocyclic compounds. Its mechanism of action involves participating in nucleophilic substitution reactions, where it can displace a leaving group from a molecule, leading to the formation of new carbon-nitrogen bonds. 2-Methoxybenzylamine′s reactivity allows for the introduction of the 2-methoxybenzylamine moiety into complex molecular structures, enabling the synthesis of diverse chemical entities. 2-Methoxybenzylamine plays an important role in the construction of novel organic molecules and the exploration of their properties.
2-Methoxybenzylamine (CAS 6850-57-3) References
- Isoquinoline-6-carboxamides as potent and selective anti-human cytomegalovirus (HCMV) inhibitors. | Chan, L., et al. 1999. Bioorg Med Chem Lett. 9: 2583-6. PMID: 10498213
- Design, synthesis, and biological evaluation of symmetrically and unsymmetrically substituted methoctramine-related polyamines as muscular nicotinic receptor noncompetitive antagonists. | Rosini, M., et al. 1999. J Med Chem. 42: 5212-23. PMID: 10602706
- Conversion of the iridoid glucoside antirrhinoside into 3-azabicyclo[3.3.0]octane building blocks. | Franzyk, H., et al. 2000. J Nat Prod. 63: 592-5. PMID: 10843565
- Traceless solid-phase synthesis of 1,2,4-triazoles using a novel amine resin. | Larsen, SD. and DiPaolo, BA. 2001. Org Lett. 3: 3341-4. PMID: 11594829
- Microwave-assisted synthesis of highly substituted aminomethylated 2-pyridones. | Pemberton, N., et al. 2004. J Org Chem. 69: 7830-5. PMID: 15527258
- Propidium-based polyamine ligands as potent inhibitors of acetylcholinesterase and acetylcholinesterase-induced amyloid-beta aggregation. | Bolognesi, ML., et al. 2005. J Med Chem. 48: 24-7. PMID: 15633997
- Metal-free metathesis reaction of C-chiral allylic sulfilimines with aryl isocyanates: construction of chiral nonracemic allylic isocyanates. | Grange, RL. and Evans, PA. 2014. J Am Chem Soc. 136: 11870-3. PMID: 25109231
- Benzylamide antagonists of protease activated receptor 2 with anti-inflammatory activity. | Yau, MK., et al. 2016. Bioorg Med Chem Lett. 26: 986-991. PMID: 26725028
- Characterization of hallucinogenic phenethylamines using high-resolution mass spectrometry for non-targeted screening purposes. | Pasin, D., et al. 2017. Drug Test Anal. 9: 1620-1629. PMID: 28133938
- A selective naked-eye chemosensor derived from 2-methoxybenzylamine and 2,3-dihydroxybenzaldehyde - synthesis, spectral characterization and electrochemistry of its bis-bidentates Schiff bases metal complexes. | Djouhra, A., et al. 2017. Spectrochim Acta A Mol Biomol Spectrosc. 184: 299-307. PMID: 28525865
- Efficient copper-catalyzed amination of DNA-conjugated aryl iodides under mild aqueous conditions. | Ruff, Y. and Berst, F. 2018. Medchemcomm. 9: 1188-1193. PMID: 30109007
- 2D sp2 Carbon-Conjugated Porphyrin Covalent Organic Framework for Cooperative Photocatalysis with TEMPO. | Shi, JL., et al. 2020. Angew Chem Int Ed Engl. 59: 9088-9093. PMID: 32162747
- Non-covalent π-π functionalized Gii-senseⓇ graphene foam for interleukin 10 impedimetric detection. | M Frias, IA., et al. 2023. Biosens Bioelectron. 222: 114954. PMID: 36502717
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-Methoxybenzylamine, 5 g | sc-238118 | 5 g | $31.00 |