All Photos(1)
About This Item
Linear Formula:
CH3C6H3(NO2)OCH3
CAS Number:
Molecular Weight:
167.16
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
97%
mp
61-64 °C (lit.)
functional group
nitro
SMILES string
COc1ccc(cc1C)[N+]([O-])=O
InChI
1S/C8H9NO3/c1-6-5-7(9(10)11)3-4-8(6)12-2/h3-5H,1-2H3
InChI key
QOZMIJZYJZQOBV-UHFFFAOYSA-N
General description
2-Methyl-4-nitroanisole is obtained as one of the products from the charge-transfer trinitromethylation of 2-methylanisole in the presence of dichloromethane.
Application
2-Methyl-4-nitroanisole may be used in the synthesis of 2-methyl-4-nitrophenol and 3-methyl-4-methoxyaniline.
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
Regulatory Information
新产品
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Studies on photochemical reaction of air pollutants. X. Identification of nitrophenols in suspended particulates.
Nojima K, et al.
Chemical & Pharmaceutical Bulletin, 31(3), 1047-1051 (1983)
Annihilation of aromatic cation radicals by ion-pair and radical pair collapse. Unusual solvent and salt effects in the competition for aromatic substitution.
Sankararaman S, et al.
Journal of the American Chemical Society, 109(25), 7824- 7838 (1987)
5-Methyl-6-methoxy-8-(2'-diethylaminoethylamino)-quinoline1.
Carmack M, et al.
Journal of the American Chemical Society, 68(8), 1551-1552 (1946)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service