516422
4-甲氧基-3-硝基苯甲醛
97%
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线性分子式:
CH3OC6H3(NO2)CHO
化学文摘社编号:
分子量:
181.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
产品名称
4-甲氧基-3-硝基苯甲醛, 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
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)
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
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.
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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