Recommended Products
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.
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
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Don't see the Right Version?
If you require a particular version, you can look up a specific certificate by the Lot or Batch number.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Indian Journal of Chemistry, 33-33 (1975)
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.
Journal of the American Chemical Society, 70(3), 1249-1253 (1948-03-01)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service