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553654

Sigma-Aldrich

4′-Methoxy-3′-nitroacetophenone

97%

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10 G
¥13,900

¥13,900


Estimated to ship onApril 04, 2025


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10 G
¥13,900

About This Item

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

¥13,900


Estimated to ship onApril 04, 2025


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Quality Level

Assay

97%

form

solid

mp

97-100 °C (lit.)

functional group

ketone
nitro

SMILES string

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

InChI

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

InChI key

VXLKYQQBEPCMJE-UHFFFAOYSA-N

General description

4′-Methoxy-3′-nitroacetophenone can be synthesized from p-methoxyacetophenone via nitration.[1]

Application

4′-Methoxy-3′-nitroacetophenone may be used to synthesize dimethylamino compound, via W2 Raney nickel catalyzed reductive methylation.[2]

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

553654-VAR:
553654-BULK:
553654-10G:
553654-50G:


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Indian Journal of Chemistry, 33-33 (1975)
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)
Qiumei Du et al.
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