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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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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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