Molecular structure of 4-Aminobenzaldehyde, CAS Number: 556-18-3
4-Aminobenzaldehyde (CAS 556-18-3)
Alternate Names:
p-Formylaniline
Application:
4-Aminobenzaldehyde is a useful synthetic reagent and monomer
CAS Number:
556-18-3
Molecular Weight:
121.14
Molecular Formula:
C7H7NO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
4-Aminobenzaldehyde (4-AB) is a useful synthetic reagent and monomer. It interacts with various proteins, enzymes, and receptors. For example, it inhibits the activity of cyclooxygenase-2 (COX-2), an enzyme involved in inflammation, and tyrosine kinase, an enzyme involved in cell proliferation. In addition, 4-Aminobenzaldehyde may act to inhibit the activity of several other enzymes, including nitric oxide synthase and 5-lipoxygenase. It is an important intermediate in the synthesis of a variety of compounds. Scientific research utilizes 4-Aminobenzaldehyde due to its antioxidant, anti-inflammatory, anti-cancer, and anti-bacterial properties.
4-Aminobenzaldehyde (CAS 556-18-3) References
- Structural characterization of pyrrolic cross-links in collagen using a biotinylated Ehrlich's reagent. | Brady, JD. and Robins, SP. 2001. J Biol Chem. 276: 18812-8. PMID: 11278513
- Chemoselective hydrogenation of nitro compounds with supported gold catalysts. | Corma, A. and Serna, P. 2006. Science. 313: 332-4. PMID: 16857934
- Preparation of substituted anilines from nitro compounds by using supported gold catalysts. | Corma, A. and Serna, P. 2006. Nat Protoc. 1: 2590-5. PMID: 17406513
- One-pot organocatalytic asymmetric synthesis of 3-nitro-1,2-dihydroquinolines by a dual-activation protocol. | Wang, YF., et al. 2009. Chem Asian J. 4: 1834-1838. PMID: 19830777
- A small molecule sensor for fluoride based on an autoinductive, colorimetric signal amplification reaction. | Baker, MS. and Phillips, ST. 2012. Org Biomol Chem. 10: 3595-9. PMID: 22456897
- Probing the role of surface energetics of electrons and their accumulation in photoreduction processes on TiO₂. | Molinari, A., et al. 2014. Chemistry. 20: 7759-65. PMID: 24829086
- Coupling Activity-Based Detection, Target Amplification, Colorimetric and Fluorometric Signal Amplification, for Quantitative Chemosensing of Fluoride Generated from Nerve Agents. | Sun, X., et al. 2017. Chemistry. 23: 3903-3909. PMID: 28117920
- Novel cellulose-based halochromic test strips for naked-eye detection of alkaline vapors and analytes. | Abou-Yousef, H., et al. 2017. Talanta. 170: 137-145. PMID: 28501149
- A Pd@Zeolite Catalyst for Nitroarene Hydrogenation with High Product Selectivity by Sterically Controlled Adsorption in the Zeolite Micropores. | Zhang, J., et al. 2017. Angew Chem Int Ed Engl. 56: 9747-9751. PMID: 28503914
- Organically Functionalized Mesoporous SBA-15 Type Material Bearing Fluorescent Sites for Selective Detection of HgII from Aqueous Medium. | Paul, L., et al. 2019. ACS Omega. 4: 17857-17863. PMID: 31681894
- A new approach for IR spectra matching using normalized local change. | Ellis, JD., et al. 2020. Anal Chim Acta. 1103: 49-57. PMID: 32081188
- ElNFS1, a nitroreductase gene from Enterobacter ludwigii, confers enhanced detoxification and phytoremediation of 4-nitrobenzaldehyde in rice. | Li, Z., et al. 2022. Environ Pollut. 314: 120292. PMID: 36181935
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
4-Aminobenzaldehyde, 5 g | sc-352378 | 5 g | $217.00 | |||
4-Aminobenzaldehyde, 25 g | sc-352378A | 25 g | $569.00 |