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133485

Sigma-Aldrich

4-Amino-1-naphthol hydrochloride

technical grade, 90%

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About This Item

Linear Formula:
H2NC10H6OH · HCl
CAS Number:
Molecular Weight:
195.65
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

Assay

90%

form

solid

mp

273 °C (dec.) (lit.)

SMILES string

Cl.Nc1ccc(O)c2ccccc12

InChI

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

InChI key

FDBQTRARWCKEJY-UHFFFAOYSA-N

Application

4-Amino-1-naphthol hydrochloride was used in the synthesis of 2-(3-aminophenol)-6-(4-amino-1-naphthol)-4-chloro-s-triazine. It was used in the synthesis of 4-aminoalkyl-1-naphthol derivatives.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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S F Teng et al.
Journal of chromatography. B, Biomedical sciences and applications, 740(1), 1-15 (2000-05-08)
A synthetic bifunctional ligand (22/8) comprising a triazine scaffold substituted with 3-aminophenol (22) and 4-amino-1-naphthol (8) has been designed, synthesised, characterised and immobilized on agarose beads to create a robust, highly selective affinity adsorbent for human immunoglobulin G (IgG). Scatchard
Ute F Röhrig et al.
Journal of medicinal chemistry, 53(3), 1172-1189 (2010-01-09)
Indoleamine 2,3-dioxygenase (IDO) is an important therapeutic target for the treatment of diseases such as cancer that involve pathological immune escape. We have used the evolutionary docking algorithm EADock to design new inhibitors of this enzyme. First, we investigated the

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