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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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
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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Anodic oxidations. VII. Nuclear cyanation of methylanisoles.
The Journal of Organic Chemistry, 40(1), 63-66 (1975)
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
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