237388
mono-Methyl 5-nitroisophthalate
99%
Synonym(s):
Monomethyl 5-nitrobenzene-1,3-dicarboxylate
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
O2NC6H3-3-(CO2H)CO2CH3
CAS Number:
Molecular Weight:
225.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-793-6
Beilstein/REAXYS Number:
1469253
MDL number:
InChI key
ZCRNIIJXDRYWDU-UHFFFAOYSA-N
InChI
1S/C9H7NO6/c1-16-9(13)6-2-5(8(11)12)3-7(4-6)10(14)15/h2-4H,1H3,(H,11,12)
SMILES string
COC(=O)c1cc(cc(c1)[N+]([O-])=O)C(O)=O
assay
99%
Application
mono-Methyl 5-nitroisophthalate has been used as starting reagent in the synthesis of 3-amide-5-[(dipropylamino)carbonyl]benzoic acids.
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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.
Steven W Kortum et al.
Bioorganic & medicinal chemistry letters, 17(12), 3378-3383 (2007-04-17)
The design and synthesis of a novel series of potent BACE1 hydroxyethylamine inhibitors. These inhibitors feature hydrogen bonding substituents at the C-5 position of the isophthalamide ring with improved selectivity over cathepsin D.
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