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Merck

164267

Sigma-Aldrich

3-氨基-2-萘酚

greener alternative

97%

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About This Item

线性分子式:
H2NC10H6OH
CAS号:
分子量:
159.18
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

環保替代產品評分

old score: 15
new score: 9
Find out more about DOZN™ Scoring

環保替代產品特色

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.)

環保替代類別

SMILES 字串

Nc1cc2ccccc2cc1O

InChI

1S/C10H9NO/c11-9-5-7-3-1-2-4-8(7)6-10(9)12/h1-6,12H,11H2

InChI 密鑰

ZHVPTERSBUMMHK-UHFFFAOYSA-N

一般說明

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.

應用

3-Amino-2-naphthol was used in the synthesis of 2-naphthyl-3-NHSO2CF3, 1-naphthyl-5-NHSO2CF3, benzoquinolinequinone and 3-chloro-2-napthol.

象形圖

Health hazardExclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

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Steven D Linton et al.
Bioorganic & medicinal chemistry letters, 12(20), 2973-2975 (2002-09-25)
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)
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)
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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