516422
4-Methoxy-3-nitrobenzaldehyde
97%
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About This Item
Linear Formula:
CH3OC6H3(NO2)CHO
CAS Number:
Molecular Weight:
181.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Product Name
4-Methoxy-3-nitrobenzaldehyde, 97%
InChI
1S/C8H7NO4/c1-13-8-3-2-6(5-10)4-7(8)9(11)12/h2-5H,1H3
SMILES string
COc1ccc(C=O)cc1[N+]([O-])=O
InChI key
YTCRQCGRYCKYNO-UHFFFAOYSA-N
assay
97%
mp
97-100 °C (lit.)
functional group
aldehyde
nitro
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Polymorphism in 4-methoxy-3-nitrobenzaldehyde.
Wishkerman S, et al.
Crystal Growth & Design, 6(6), 1366-1373 (2006)
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.
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)
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
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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