Date published: 2026-4-25

1-800-457-3801

SCBT Portrait Logo
Seach Input

4-[(N-Boc)aminomethyl]aniline (CAS 94838-55-8)

0.0(0)
Write a reviewAsk a question

Alternate Names:
tert-Butyl 4-aminobenzylcarbamate
Application:
4-[(N-Boc)aminomethyl]aniline is an aniline derivative
CAS Number:
94838-55-8
Molecular Weight:
222.28
Molecular Formula:
C12H18N2O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

4-[(N-Boc)aminomethyl]aniline is widely used in organic synthesis, particularly in the modification of amine functionalities. This chemical is integral in the creation of advanced intermediates for complex molecule construction. In the realm of polymer research, 4-[(N-Boc)aminomethyl]aniline contributes to the development of new polymeric materials by providing a protected amine group that can be selectively deprotected to react with various monomers. Additionally, it plays a significant role in the study of dye and pigment synthesis, where it acts as a precursor for compounds requiring specific structural features for color properties. Research involving 4-[(N-Boc)aminomethyl]aniline also extends to surface modification techniques, where it is used to alter the chemical properties of surfaces for improved adhesion or reactivity.


4-[(N-Boc)aminomethyl]aniline (CAS 94838-55-8) References

  1. High-throughput screening of small molecule ligands targeted to live bacteria surface.  |  Lee, JH., et al. 2013. Anal Chem. 85: 3508-14. PMID: 23461528
  2. Identification and SAR Evaluation of Hemozoin-Inhibiting Benzamides Active against Plasmodium falciparum.  |  Wicht, KJ., et al. 2016. J Med Chem. 59: 6512-30. PMID: 27299916
  3. Convergent Synthesis of Two Fluorescent Ebselen-Coumarin Heterodimers.  |  Küppers, J., et al. 2016. Pharmaceuticals (Basel). 9: PMID: 27399725
  4. Identification and Structure-Activity Relationships of Novel Compounds that Potentiate the Activities of Antibiotics in Escherichia coli.  |  Haynes, KM., et al. 2017. J Med Chem. 60: 6205-6219. PMID: 28650638
  5. Single-walled carbon nanotubes-ciprofloxacin nanoantibiotic: strategy to improve ciprofloxacin antibacterial activity.  |  Assali, M., et al. 2017. Int J Nanomedicine. 12: 6647-6659. PMID: 28924348
  6. Imaging carbon nanostructures' reactivity: a complementary strategy to define chemical structure.  |  Pérez-Luna, V., et al. 2018. R Soc Open Sci. 5: 180605. PMID: 30225055
  7. Interphase Engineering of a Cellulose-Based Carbon Fiber Reinforced Composite by Applying Click Chemistry.  |  Szabó, L., et al. 2018. ChemistryOpen. 7: 720-729. PMID: 30258744
  8. Lignin as a Functional Green Coating on Carbon Fiber Surface to Improve Interfacial Adhesion in Carbon Fiber Reinforced Polymers.  |  Szabó, L., et al. 2019. Materials (Basel). 12: PMID: 30621362
  9. Sensitive analysis of fatty acid esters of hydroxy fatty acids in biological lipid extracts by shotgun lipidomics after one-step derivatization.  |  Hu, C., et al. 2020. Anal Chim Acta. 1105: 105-111. PMID: 32138907
  10. Fragment-Based Design of Mycobacterium tuberculosis InhA Inhibitors.  |  Sabbah, M., et al. 2020. J Med Chem. 63: 4749-4761. PMID: 32240584
  11. Carbon fibre reinforced cellulose-based polymers: intensifying interfacial adhesion between the fibre and the matrix.  |  Szabó, L., et al. 2018. RSC Adv. 8: 22729-22736. PMID: 35539726
  12. Photochromic Fentanyl Derivatives for Controlled μ-Opioid Receptor Activation.  |  Lahmy, R., et al. 2022. Chemistry. 28: e202201515. PMID: 35899620
  13. Distribution in the brain and possible neuroprotective effects of intranasally delivered multi-walled carbon nanotubes.  |  Soligo, M., et al. 2021. Nanoscale Adv. 3: 418-431. PMID: 36131737

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-[(N-Boc)aminomethyl]aniline, 1 g

sc-254588
1 g
$49.00