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About This Item
Linear Formula:
CH3OC6H3(NO2)CHO
CAS Number:
Molecular Weight:
181.15
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
97%
mp
97-100 °C (lit.)
SMILES string
COc1ccc(C=O)cc1[N+]([O-])=O
InChI
1S/C8H7NO4/c1-13-8-3-2-6(5-10)4-7(8)9(11)12/h2-5H,1H3
InChI key
YTCRQCGRYCKYNO-UHFFFAOYSA-N
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
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Joshua R Ring et al.
Acta crystallographica. Section C, Crystal structure communications, 63(Pt 7), o392-o394 (2007-07-05)
In the title compound, C(9)H(12)N(5)O(3)(+) x Cl(-), the cation is almost entirely planar. The imine double bond is exclusively in the E geometry.
Polymorphism in 4-methoxy-3-nitrobenzaldehyde.
Wishkerman S, et al.
Crystal Growth & Design, 6(6), 1366-1373 (2006)
Xiaojun Han et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(28), 7957-7964 (2007-07-06)
This work demonstrates the use of photocleavable cholesterol derivatives to create supported bilayer lipid membrane arrays on silica. The photocleavable cholesteryl tether is attached to the surface by using the reaction of an amine-functionalized self-assembled monolayer (SAM) and the N-hydroxysuccinimide-based
Tele nucleophilic aromatic substitutions in 1-nitro-3-and 1, 3-dinitro-5-trichloromethylbenzene, and 3-trichloromethylbenzonitrile. A new synthesis of the 1, 4-benzothiazine-3 (4H)-one ring system from 3-nitrobenzoic acid.
Giannopoulos T, et al.
Tetrahedron, 56(3), 447-453 (2000)
Synthesis, cytotoxic activity and docking studies of new 4-aza-podophyllotoxin derivatives.
Hatti I, et al.
Medicinal Chemistry Research, 24(8), 3305-3313 (2015)
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