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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)

Anticancer effects of four varieties of muscadine grape.

Jason M God et al.

Journal of medicinal food, 10(1), 54-59 (2007-05-03)

The initiating event in carcinogenesis is a somatic mutation. During progression of the disease, additional mutations accumulate as the transformed cells develop the ability to proliferate and metastasize. These mutations can be produced by reactive oxygen species (ROS) generated through

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Global Trade Item Number

SKU	GTIN
A38800-25G	04061832089034
A38800-5G	04061833368145
A38800-1G	04061833368138