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Merck
CN

174556

4-甲氧基-1-萘酚

≥97%

别名:

1-羟基-4-甲氧基萘

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关于此项目

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:
Assay:
≥97%
Form:
solid
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assay

≥97%

form

solid

mp

126-129 °C (lit.)

SMILES string

COc1ccc(O)c2ccccc12

InChI

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

InChI key

BOTGCZBEERTTDQ-UHFFFAOYSA-N

Application

4-Methoxy-1-naphthol was used in the synthesis of 3-(4-hydroxy-1-naphthoxy)lactic acid (4-HO-NLA).


pictograms

Exclamation mark

signalword

Warning

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



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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



全球贸易项目编号

货号GTIN
174556-5G04061838752017
174556-25G04061832879895