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Merck
CN

553654

4′-Methoxy-3′-nitroacetophenone

97%

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About This Item

Linear Formula:
CH3OC6H3(NO2)C(O)CH3
CAS Number:
Molecular Weight:
195.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
228-476-7
MDL number:
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Product Name

4′-Methoxy-3′-nitroacetophenone, 97%

InChI key

VXLKYQQBEPCMJE-UHFFFAOYSA-N

InChI

1S/C9H9NO4/c1-6(11)7-3-4-9(14-2)8(5-7)10(12)13/h3-5H,1-2H3

SMILES string

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

assay

97%

form

solid

mp

97-100 °C (lit.)

functional group

ketone
nitro

Quality Level

Application

4′-Methoxy-3′-nitroacetophenone may be used to synthesize dimethylamino compound, via W2 Raney nickel catalyzed reductive methylation.

General description

4′-Methoxy-3′-nitroacetophenone can be synthesized from p-methoxyacetophenone via nitration.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Indian Journal of Chemistry, 33-33 (1975)
Qiumei Du et al.
Developmental cell, 49(4), 618-631 (2019-04-16)
MicroRNAs (miRNAs) are processed from primary miRNA transcripts (pri-miRNAs), many of which are annotated as long noncoding RNAs (lncRNAs). We assessed whether MIR205HG, the host gene for miR-205, has independent functions as an lncRNA. Comparing mice with targeted deletions of MIR205HG and
Structure determination and synthesis of a plant growth inhibitor, 3-acetyl-6-methoxybenzaldehyde, found in the leaves of Encelia farinosa.
R GRAY et al.
Journal of the American Chemical Society, 70(3), 1249-1253 (1948-03-01)

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