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Safety Information

537837

Sigma-Aldrich

2-Methyl-4-nitroanisole

97%

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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

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.

Pictograms

Exclamation mark

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 Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

537837-VAR:
537837-BULK:
537837-1G:
537837-10G:


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5-Methyl-6-methoxy-8-(2'-diethylaminoethylamino)-quinoline1.
Carmack M, et al.
Journal of the American Chemical Society, 68(8), 1551-1552 (1946)
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)

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