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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:
Recommended Products
Quality Level
Assay
97%
form
solid
mp
97-100 °C (lit.)
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
Related Categories
General description
4′-Methoxy-3′-nitroacetophenone can be synthesized from p-methoxyacetophenone via nitration.
Application
4′-Methoxy-3′-nitroacetophenone may be used to synthesize dimethylamino compound, via W2 Raney nickel catalyzed reductive methylation.
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
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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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.
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
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