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634859

Sigma-Aldrich

3-Methoxy-2-naphthol

97%

Synonym(s):

2-Hydroxy-3-methoxynaphthalene

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About This Item

Linear Formula:
CH3OC10H6OH
CAS Number:
18515-11-2
Molecular Weight:
174.20
MDL number:
MFCD00029345
UNSPSC Code:
12352100
PubChem Substance ID:
24882696
NACRES:
NA.22

assay

97%

form

solid

mp

107-111 °C (lit.)

SMILES string

COc1cc2ccccc2cc1O

InChI

1S/C11H10O2/c1-13-11-7-9-5-3-2-4-8(9)6-10(11)12/h2-7,12H,1H3

InChI key

SJTNTIRIRIPZDV-UHFFFAOYSA-N

Application

3-Methoxy-2-naphthol can be used in the synthesis of a naphthoate ester, which can act like dopamine D4 antagonist.[1]

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
33697LJ
09730AJ
04801CH
09327KB

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Design and synthesis of 2-naphthoate esters as selective dopamine D4 antagonists.
I Boyfield et al.
Journal of medicinal chemistry, 39(10), 1946-1948 (1996-05-10)
Nick D Pokorzynski et al.
eLife, 8 (2019-04-03)
During infection, pathogens are starved of essential nutrients such as iron and tryptophan by host immune effectors. Without conserved global stress response regulators, how the obligate intracellular bacterium Chlamydia trachomatis arrives at a physiologically similar 'persistent' state in response to
Nenad Manevski et al.
Drug metabolism and disposition: the biological fate of chemicals, 43(1), 126-139 (2014-10-24)
Although skin is the largest organ of the human body, cutaneous drug metabolism is often overlooked, and existing experimental models are insufficiently validated. This proof-of-concept study investigated phase II biotransformation of 11 test substrates in fresh full-thickness human skin explants

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