164267
3-Amino-2-naphthol
97%
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About This Item
Linear Formula:
H2NC10H6OH
CAS Number:
Molecular Weight:
159.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
226-519-4
MDL number:
Assay:
97%
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
SMILES string
Nc1cc2ccccc2cc1O
InChI
1S/C10H9NO/c11-9-5-7-3-1-2-4-8(7)6-10(9)12/h1-6,12H,11H2
InChI key
ZHVPTERSBUMMHK-UHFFFAOYSA-N
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.
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.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Related Content
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
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.
Itoh S, et al.
The Journal of Organic Chemistry, 57(16), 4452-4457 (1992)
The synthesis and spectroscopic properties of some halogeno-1, 2-naphthoquinones.
Oliver RWA, et al.
Tetrahedron, 24(10), 4067-4072 (1968)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 164267-1G | 04061838748010 |
| 164267-5G | 04061838748027 |