274542
2-Bromo-2′-nitroacetophenone
99%
Synonym(s):
2′-Nitrophenacyl bromide
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
O2NC6H4COCH2Br
CAS Number:
Molecular Weight:
244.04
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
2-Bromo-2′-nitroacetophenone, 99%
InChI
1S/C8H6BrNO3/c9-5-8(11)6-3-1-2-4-7(6)10(12)13/h1-4H,5H2
SMILES string
[O-][N+](=O)c1ccccc1C(=O)CBr
InChI key
SGXUUCSRVVSMGK-UHFFFAOYSA-N
assay
99%
mp
55-57 °C (lit.)
functional group
bromo
ketone
nitro
Application
2-Bromo-2′-nitroacetophenone, an electroactive derivative-forming reagent, was used as a precolumn reagent for preparing prostaglandin derivatives.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
G M Beck et al.
Talanta, 36(3), 373-377 (1989-03-01)
Conventional reversed-phase HPLC conditions have been optimized for resolution of a mixture containing prostaglandins PGE(1), PGE(2), PGF(1alpha), and PGF(2alpha). Electroactive derivative-forming reagents, such as p-nitrobenzyloxyamine, 2-bromo-2'-nitroacetophenone, and 2,4-dinitrophenylhydrazine have been evaluated for use as precolumn reagents for forming prostaglandin derivatives.
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