A77903
1-Aminopyrene
97%
Synonym(s):
1-Pyrenamine, 3-Aminopyrene
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About This Item
Empirical Formula (Hill Notation):
C16H11N
CAS Number:
Molecular Weight:
217.27
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
216-521-3
Beilstein/REAXYS Number:
1875737
MDL number:
Assay:
97%
Form:
powder
InChI key
YZVWKHVRBDQPMQ-UHFFFAOYSA-N
InChI
1S/C16H11N/c17-14-9-7-12-5-4-10-2-1-3-11-6-8-13(14)16(12)15(10)11/h1-9H,17H2
SMILES string
Nc1ccc2ccc3cccc4ccc1c2c34
assay
97%
form
powder
mp
115-117 °C (lit.)
Quality Level
Related Categories
Application
- Synthesis and evaluation of aromatic stationary phases based on linear solvation energy relationship model for expanded application in supercritical fluid chromatography.: Explores the use of 1-Aminopyrene in the development of advanced stationary phases for chromatography, enhancing the efficiency and application range in pharmaceutical and environmental analysis (Ge et al., 2024).
- Two-Dimensional Porphyrinic Metal-Organic Framework Composites as a Photocatalytic Platform for Chemoselective Hydrogenation.: Highlights the integration of 1-Aminopyrene into metal-organic frameworks, providing a new avenue for creating highly efficient photocatalytic systems for organic synthesis, relevant to both academic research and industrial chemical manufacturing (Dong et al., 2023).
- Exploiting and Engineering Neuroglobin for Catalyzing Carbene N-H Insertions and the Formation of Quinoxalinones.: Discusses the role of 1-Aminopyrene in enhancing enzymatic reactions within engineered proteins, paving the way for novel synthetic pathways in pharmaceutical research (Sun et al., 2023).
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Dina Mukha et al.
ChemSusChem, 13(10), 2684-2692 (2020-02-19)
The construction of bias- and donor-free photobioelectrochemical cells for the generation of light-triggered electrical power is presented. The developed oxygen reduction biocathodes are based on bilirubin oxidase (BOD) that originates from Myrothecium verrucaria (MvBOD) and a thermophilic Bacillus pumilus (BpBOD).
Man Jae Park et al.
Chemical communications (Cambridge, England), 48(89), 11008-11010 (2012-10-06)
Excess electron transfer dynamics in DNA hairpins was investigated by femtosecond laser flash photolysis of a donor-DNA-acceptor system using N,N-dimethylaminopyrene and diphenylacetylene as an electron donor and acceptor, respectively. It was revealed that the excess electron hopping rate between T's
Susan Huyck et al.
Journal of exposure science & environmental epidemiology, 20(7), 650-655 (2010-05-06)
Biomonitoring of exposures to toxins is an important tool for monitoring public health and safety. Using this tool, exposures are typically measured by the collection of biological specimens such as blood and urine samples. Urine sampling represents a more convenient
Junkuo Gao et al.
Dalton transactions (Cambridge, England : 2003), 41(39), 12185-12191 (2012-08-30)
A novel pyrene covalently-attached polyoxometalate (POM) hybrid has been synthesized and fully characterized. The attractive electronic and photophysical properties of pyrene derivatives make the hybrid promising for studying and understanding electron transfer mechanisms in organic-functionalized POMs. The hybrid has an
P D Josephy et al.
Mutation research, 429(2), 199-208 (1999-10-20)
The mutagenic actions of many chemicals depend on the activities of bacterial "mutagenesis proteins", which allow replicative bypass of DNA lesions. Genes encoding these proteins occur on bacterial chromosomes and plasmids, often in the form of an operon (such as
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