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A38800

2-Aminoanthracene

Name: 2-Aminoanthracene
Brand: ALDRICH

96%

Synonym(s):

2-Anthramine

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About This Item

Empirical Formula (Hill Notation):

C₁₄H₁₁N

CAS Number:

613-13-8

Molecular Weight:

193.24

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24890821

EC Number:

210-330-9

Beilstein/REAXYS Number:

2209414

MDL number:

MFCD00003582

Assay:

96%

Form:

powder

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Properties

Quality Level

100

assay

96%

form

powder

mp

238-241 °C (lit.)

SMILES string

Nc1ccc2cc3ccccc3cc2c1

InChI

1S/C14H11N/c15-14-6-5-12-7-10-3-1-2-4-11(10)8-13(12)9-14/h1-9H,15H2

InChI key

YCSBALJAGZKWFF-UHFFFAOYSA-N

Description

Application

2-Aminoanthracene can be used as a reactant to prepare:

Steroid derived naphthoquinoline asphaltene compounds via multicomponent cyclocondensation reaction with 5-α-cholestan-3-one and aromatic aldehydes.
Naphtho[2,3- f ]quinoline derivatives by reacting with aromatic aldehyde and acetone or acetophenone catalyzed by iodine.

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

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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Steroid-Derived Naphthoquinoline Asphaltene Model Compounds: Hydriodic Acid Is the Active Catalyst in I2-Promoted Multicomponent Cyclocondensation Reactions

Schulze M, et al.

Organic Letters, 17(23), 5930-5933 (2015)

An efficient method for the synthesis of naphthoquinoline derivatives catalyzed by iodine

Wang W, et al.

Heterocyclic Communications, 18(1), 17-21 (2012)

Two-step synthesis of achiral dispiro-1,2,4,5-tetraoxanes with outstanding antimalarial activity, low toxicity, and high-stability profiles.

Gemma L Ellis et al.

Journal of medicinal chemistry, 51(7), 2170-2177 (2008-03-18)

A rapid, two-step synthesis of a range of dispiro-1,2,4,5-tetraoxanes with potent antimalarial activity both in vitro and in vivo has been achieved. These 1,2,4,5-tetraoxanes have been proven to be superior to 1,2,4-trioxolanes in terms of stability and to be superior

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