产品名称
3-氨基-2-萘酚, 97%
InChI key
ZHVPTERSBUMMHK-UHFFFAOYSA-N
InChI
1S/C10H9NO/c11-9-5-7-3-1-2-4-8(7)6-10(9)12/h1-6,12H,11H2
SMILES string
Nc1cc2ccccc2cc1O
assay
97%
greener alternative product score
old score: 15
new score: 9
Find out more about DOZN™ Scoring
greener alternative product characteristics
Atom Economy
Design for Energy Efficiency
Use of Renewable Feedstocks
Reduce Derivatives
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
mp
229-230 °C (lit.)
greener alternative category
Application
3-Amino-2-naphthol was used in the synthesis of 2-naphthyl-3-NHSO2CF3, 1-naphthyl-5-NHSO2CF3, benzoquinolinequinone and 3-chloro-2-napthol.
General description
We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product belongs to category of Re-engineered products, showing key improvements in Green Chemistry Principles “Atom economy”, “Design for Energy Efficiency”, “Use of Renewable Feedstock” and “Reduce Derivatives”. Click here to view its DOZN scorecard.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Synthesis and characterization of dimethyl 9, 10-dihydro-9, 10-dioxobenzo [f] quinoline-2, 4-dicarboxylate. Effect of the pyrrole nucleus on the reactivity of coenzyme PQQ.
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A new structural class of broad spectrum caspase inhibitors was optimized for its activity against caspases 1, 3, 6, 7, and 8. The most potent compound had low nanomolar broad spectrum activity, in particular, single digit nanomolar inhibitory activity against
The synthesis and spectroscopic properties of some halogeno-1, 2-naphthoquinones.
Oliver RWA, et al.
Tetrahedron, 24(10), 4067-4072 (1968)
H U Meisch et al.
Analytical biochemistry, 149(1), 29-34 (1985-08-15)
5-Aminolevulinic acid (ALA), the common precursor of all naturally occurring tetrapyrroles, forms a stable condensation product with 2-amino-3-hydroxynaphthalene which can be identified by its fluorescence. Separation of the compound by reversed-phase high-performance liquid chromatography on RPC-18 columns allows its detection
Renzo P Zanocco et al.
PloS one, 13(7), e0200006-e0200006 (2018-07-03)
In this study, we report the synthesis and the photochemical behavior of a series of new "click-on" fluorescent probes designed to detect singlet oxygen. They include a highly fluorescent chemical structure, an aryloxazole ring, linked to a furan moiety operating
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