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线性分子式:
CH3OC10H6OH
化学文摘社编号:
分子量:
174.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-566-3
Beilstein/REAXYS Number:
1818465
MDL number:
产品名称
4-甲氧基-1-萘酚, ≥97%
InChI key
BOTGCZBEERTTDQ-UHFFFAOYSA-N
InChI
1S/C11H10O2/c1-13-11-7-6-10(12)8-4-2-3-5-9(8)11/h2-7,12H,1H3
SMILES string
COc1ccc(O)c2ccccc12
assay
≥97%
form
solid
mp
126-129 °C (lit.)
Quality Level
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Application
4-Methoxy-1-naphthol was used in the synthesis of 3-(4-hydroxy-1-naphthoxy)lactic acid (4-HO-NLA).
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
R E Talaat et al.
Drug metabolism and disposition: the biological fate of chemicals, 14(2), 202-207 (1986-03-01)
The formation of 3-(4-hydroxy-1-naphthoxy)lactic acid (4-HO-NLA) from propranolol was investigated. Authentic 4-HO-NLA was synthesized from 4-methoxy-1-naphthol using methods previously used for preparation of naphthoxylactic acid (NLA). Cleavage of the 4-methyl ether was accomplished using iodotrimethylsilane in the presence of cyclopentene.
Denilson F Oliveira et al.
Experimental parasitology, 199, 17-23 (2019-02-23)
Exposing second-stage juveniles (J2) of Meloidogyne incognita in vitro to a phenolic compound sometimes fails to cause J2 mortality, but in tests in vivo the same compound may reduce the infectivity and population of the nematode. This work aimed to
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