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516422

Sigma-Aldrich

4-Methoxy-3-nitrobenzaldehyde

97%

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About This Item

Linear Formula:
CH3OC6H3(NO2)CHO
CAS Number:
31680-08-7
Molecular Weight:
181.15
MDL number:
MFCD00126498
UNSPSC Code:
12352100
PubChem Substance ID:
24873889
NACRES:
NA.22

Assay

97%

mp

97-100 °C (lit.)

functional group

aldehyde
nitro

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBR4377V
MKBG3674V
MKBF0721V
30096LJ
06716HJ

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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
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)
Synthesis, cytotoxic activity and docking studies of new 4-aza-podophyllotoxin derivatives.
Hatti I, et al.
Medicinal Chemistry Research, 24(8), 3305-3313 (2015)
Polymorphism in 4-methoxy-3-nitrobenzaldehyde.
Wishkerman S, et al.
Crystal Growth & Design, 6(6), 1366-1373 (2006)

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