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205664

Sigma-Aldrich

1′-Hydroxy-2′-acetonaphthone

99%

Synonym(s):

2-Acetyl-1-naphthol

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About This Item

Linear Formula:
HOC10H6COCH3
CAS Number:
711-79-5
Molecular Weight:
186.21
EC Number:
211-918-8
MDL number:
MFCD00003963
UNSPSC Code:
12352100
PubChem Substance ID:
24852216
NACRES:
NA.22

Assay

99%

form

solid

mp

98-100 °C (lit.)

SMILES string

CC(=O)c1ccc2ccccc2c1O

InChI

1S/C12H10O2/c1-8(13)10-7-6-9-4-2-3-5-11(9)12(10)14/h2-7,14H,1H3

InChI key

JBGJVMVWYWUVOW-UHFFFAOYSA-N

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General description

The modulation of different photophysical properties of 1′-hydroxy-2′-acetonaphthone (HAN), after encapsulating into the hydrophobic nanocavities of various bile salt aggregates, was studied.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

Certificates of Analysis (COA)

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Sarthak Mandal et al.
The journal of physical chemistry. B, 116(30), 8780-8792 (2012-06-19)
The modulation of the photophysical properties of 1'-hydroxy-2'-acetonaphthone (HAN) upon encapsulation into the hydrophobic nanocavities of different bile salt aggregates has been investigated for the first time using steady-state and time-resolved fluorescence spectroscopy. Because HAN is very sensitive to the
Ming-Peng Zhuo et al.
Nanoscale, 10(11), 5140-5147 (2018-03-01)
The controlled fabrication of organic single-crystalline nanowires (OSCNWs) with a uniform diameter in the nanoscale via the bottom-up approach, which is just based on weak intermolecular interaction, is a great challenge. Herein, we utilize the synergy approach of the bottom-up
Gamze Bora-Tatar et al.
Bioorganic & medicinal chemistry, 17(14), 5219-5228 (2009-06-13)
In the light of known HDAC inhibitors, 33 carboxylic acid derivatives were tested to understand the structural requirements for HDAC inhibition activity. Several modifications were applied to develop the structure-activity relationships of carboxylic acid HDAC inhibitors. HDAC inhibition activities were

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