553654
4′-甲氧基-3′-硝基苯乙酮
97%
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关于此项目
线性分子式:
CH3OC6H3(NO2)C(O)CH3
化学文摘社编号:
分子量:
195.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
228-476-7
MDL number:
产品名称
4′-甲氧基-3′-硝基苯乙酮, 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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
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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