213187
5-硝基-2-甲基苯甲醚
99%
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关于此项目
线性分子式:
CH3C6H3(NO2)OCH3
化学文摘社编号:
分子量:
167.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
236-048-6
MDL number:
Assay:
99%
assay
99%
mp
69-71 °C (lit.)
SMILES string
COc1cc(ccc1C)[N+]([O-])=O
InChI
1S/C8H9NO3/c1-6-3-4-7(9(10)11)5-8(6)12-2/h3-5H,1-2H3
InChI key
WVQGZNRUEVFXKR-UHFFFAOYSA-N
Application
2-Methyl-5-nitroanisole was used in the synthesis of:
- 2-methoxy-p-toluidine via reduction with tin and hydrochloric acid
- 2-methoxy-4-nitrobenzyl bromide
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
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
法规信息
新产品
此项目有
Anodic oxidations. VII. Nuclear cyanation of methylanisoles.
Yoshida K, et al.
The Journal of Organic Chemistry, 40(1), 63-66 (1975)
P K Chakraborty et al.
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 42(7), 673-681 (1991-01-01)
The synthesis of 4-[18F]fluoroguaiacol (4-[18F]fluoro-2-methoxyphenol) has been achieved in no-carrier-added form starting from 2-methoxy-4-nitrobenzaldehyde, using nucleophilic aromatic substitution by [18F]fluoride followed by Baeyer-Villiger oxidation of the benzaldehyde to the phenol. Demethylation with boron tribromide gave 4-[18F]fluorocatechol (1,2-dihydroxy-4-[18F]fluorobenzene) with an overall
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 213187-10G | 04061838772619 |
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