Molecular structure of 2-Aminophenol, CAS Number: 95-55-6
2-Aminophenol (CAS 95-55-6)
Alternate Names:
2-Hydroxyaniline
CAS Number:
95-55-6
Purity:
≥98%
Molecular Weight:
109.13
Molecular Formula:
C6H7NO
Supplemental Information:
This is classified 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.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
2-Aminophenol is a chemical compound that functions as a reagent in various organic synthesis reactions. It acts as a precursor in the production of dyes, and other organic compounds. In the experimental, 2-Aminophenol participates in nucleophilic aromatic substitution reactions, where it undergoes substitution with electrophiles to form new carbon-carbon or carbon-heteroatom bonds. 2-Aminophenol′s mechanism of action involves its ability to donate a lone pair of electrons from the amino group, facilitating the formation of new chemical bonds. 2-Aminophenol can undergo oxidation to form quinone derivatives, which are important intermediates in the synthesis of various organic compounds. Its reactivity and ability to undergo diverse chemical transformations make it a versatile building block in organic synthesis and development.
2-Aminophenol (CAS 95-55-6) References
- Genetic and biochemical comparison of 2-aminophenol 1,6-dioxygenase of Pseudomonas pseudoalcaligenes JS45 to meta-cleavage dioxygenases: divergent evolution of 2-aminophenol meta-cleavage pathway. | Davis, JK., et al. 1999. Arch Microbiol. 172: 330-9. PMID: 10550475
- A novel 2-aminophenol 1,6-dioxygenase involved in the degradation of p-chloronitrobenzene by Comamonas strain CNB-1: purification, properties, genetic cloning and expression in Escherichia coli. | Wu, JF., et al. 2005. Arch Microbiol. 183: 1-8. PMID: 15580337
- Genomic and functional analyses of the 2-aminophenol catabolic pathway and partial conversion of its substrate into picolinic acid in Burkholderia xenovorans LB400. | Chirino, B., et al. 2013. PLoS One. 8: e75746. PMID: 24124510
- Oxygenative aromatic ring cleavage of 2-aminophenol with dioxygen catalyzed by a nonheme iron complex: catalytic functional model of 2-aminophenol dioxygenases. | Chatterjee, S. and Paine, TK. 2015. Inorg Chem. 54: 1720-7. PMID: 25646806
- Mechanistic studies of the tyrosinase-catalyzed oxidative cyclocondensation of 2-aminophenol to 2-aminophenoxazin-3-one. | Washington, C., et al. 2015. Arch Biochem Biophys. 577-578: 24-34. PMID: 25982123
- Highly sensitive and simultaneous electrochemical determination of 2-aminophenol and 4-aminophenol based on poly(l-arginine)-β-cyclodextrin/carbon nanotubes@graphene nanoribbons modified electrode. | Yi, Y., et al. 2016. Biosens Bioelectron. 77: 353-8. PMID: 26433068
- Oxidation of 2-aminophenol to 2-amino-3H-phenoxazin-3-one with monochloramine in aqueous environment: A new method for APO synthesis? | Abou Mehrez, O., et al. 2016. Chemosphere. 145: 464-9. PMID: 26694797
- Dioxygen Reactivity of an Iron Complex of 2-Aminophenol-Appended Ligand: Crystallographic Evidence of the Aromatic Ring Cleavage Product of the 2-Aminophenol Unit. | Paul, GC., et al. 2017. Inorg Chem. 56: 729-736. PMID: 28005345
- One-Pot Synthesis of 3-Difluoromethyl Benzoxazole-2-thiones. | Li, Z., et al. 2018. Org Lett. 20: 6407-6410. PMID: 30303015
- Tailoring the heterojunction of TiO2 with multivalence CeO2 nanocrystals - for detection of toxic 2-aminophenol. | Manoj, D., et al. 2022. Food Chem Toxicol. 165: 113182. PMID: 35643232
- 2-aminophenol 1,6-dioxygenase: a novel aromatic ring cleavage enzyme purified from Pseudomonas pseudoalcaligenes JS45. | Lendenmann, U. and Spain, JC. 1996. J Bacteriol. 178: 6227-32. PMID: 8892823
- Novel genes encoding 2-aminophenol 1,6-dioxygenase from Pseudomonas species AP-3 growing on 2-aminophenol and catalytic properties of the purified enzyme. | Takenaka, S., et al. 1997. J Biol Chem. 272: 14727-32. PMID: 9169437
- Metabolism of 2-aminophenol by Pseudomonas sp. AP-3: modified meta-cleavage pathway. | Takenaka, S., et al. 1998. Arch Microbiol. 170: 132-7. PMID: 9683650
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-Aminophenol, 5 g | sc-237913 | 5 g | $29.00 |