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367699

Sigma-Aldrich

4-Methyl-2-nitroanisole

99%

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100 ML
$224.00

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100 ML
$224.00

About This Item

Linear Formula:
CH3C6H3(NO2)OCH3
CAS Number:
119-10-8
Molecular Weight:
167.16
EC Number:
204-296-4
MDL number:
MFCD00024540
UNSPSC Code:
12352100
PubChem Substance ID:
24862822
NACRES:
NA.22

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Quality Level

100

assay

99%

form

liquid

refractive index

n20/D 1.557 (lit.)

bp

154 °C/14 mmHg (lit.)

mp

8-9 °C (lit.)

density

1.205 g/mL at 25 °C (lit.)

functional group

nitro

SMILES string

COc1ccc(C)cc1[N+]([O-])=O

InChI

1S/C8H9NO3/c1-6-3-4-8(12-2)7(5-6)9(10)11/h3-5H,1-2H3

Inchi Key

LGNMURXRPLMVJI-UHFFFAOYSA-N

Related Categories

General description

Nucleophilic substitution reactions of 4-methyl-2-nitroanisole in neat cyclohexylamine and piperidine have been reported.[1]

Application

4-Methyl-2-nitroanisole may be used in the synthesis of 1-dibromomethyl-4-methoxy-2-nitrobenzene.[2]

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW6417
MKCL7686
MKCD1934
MKBW1329V
MKBC0630

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Hoong-Kun Fun et al.
Acta crystallographica. Section E, Structure reports online, 65(Pt 9), o2193-o2194 (2009-01-01)
The asymmetric unit of the title compound, C(8)H(7)Br(2)NO(3), comprises two crystallographically independent mol-ecules (A and B). The nitro groups are twisted from the attached benzene rings, making dihedral angles of 39.26 (9) and 35.90 (9)° in mol-ecules A and B, respectively. In
Theoretical calculations of chemical interactions. Part 4. Aromatic nucleophilic substitutions and SN 2 reactions of 4-and 6-substituted 2-nitroanisoles.
Nudelman NS and Palleros DR.
J. Chem. Soc. Perkin Trans. II, 6, 805-809 (1985)
Yusuke Yamamoto et al.
The Journal of toxicological sciences, 44(9), 585-600 (2019-09-03)
Amino acid derivative reactivity assay (ADRA) has previously been developed as an alternative method to direct peptide reactivity assay (DPRA) to evaluate key event 1 in skin sensitization mechanisms. However, when using alternative methods for skin sensitization, integrated approaches to

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