428507
5-(2-硝基苯)糠醛
99%
别名:
5-(2-硝基苯)-2-呋喃甲醛
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关于此项目
经验公式（希尔记法）:
C11H7NO4
化学文摘社编号:
分子量:
217.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
solid
产品名称
5-(2-硝基苯)糠醛, 99%
InChI
1S/C11H7NO4/c13-7-8-5-6-11(16-8)9-3-1-2-4-10(9)12(14)15/h1-7H
SMILES string
[H]C(=O)c1ccc(o1)-c2ccccc2[N+]([O-])=O
InChI key
QBYRUURYXPVDAK-UHFFFAOYSA-N
assay
99%
form
solid
bp
105-107 °C/30 mmHg (lit.)
mp
94-97 °C (lit.)
functional group
aldehyde
nitro
Quality Level
Application
5-(2-Nitrophenyl)furfural (5-(2-nitrophenyl)-2-furfuraldehyde) was used in the synthesis of (5-(2-nitrophenyl)furfuran-2-yl)methanol.
It may be used in the synthesis of 2-{[5-(2-nitrophenyl)furan-2-yl]methyleneamino}benzoic acid (HOBZ) by reacting with 2-aminobenzoic acid.
It may be used in the synthesis of 2-{[5-(2-nitrophenyl)furan-2-yl]methyleneamino}benzoic acid (HOBZ) by reacting with 2-aminobenzoic acid.
General description
5-(2-Nitrophenyl)furfural is a furfural derivative.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
New di-and triorganotin (IV) carboxylates derived from a Schiff base: synthesis, characterization and in vitro antimicrobial activities.
Dias LC, et al.
Applied Organometallic Chemistry, 29(5), 305-313 (2015)
Ruthenium (II)-Catalyzed Transfer Hydrogenation of Aromatic and Heteroaromatic Aldehydes in Air.
Bhosale SS and Singh KS.
Synthetic Communications, 45(12), 1-10 (2015)
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