191434
4-硝基苯甲胺 盐酸盐
97%
别名:
(4-Nitrophenyl)methanamine hydrochloride, 4-Nitrobenzenemethanamine hydrochloride, p-Nitrobenzylamine hydrochloride
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关于此项目
线性分子式:
O2NC6H4CH2NH2 · HCl
化学文摘社编号:
分子量:
188.61
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
242-441-3
Beilstein/REAXYS Number:
3629994
MDL number:
Assay:
97%
Form:
solid
InChI key
SMIXZZMSWYOQPW-UHFFFAOYSA-N
InChI
1S/C7H8N2O2.ClH/c8-5-6-1-3-7(4-2-6)9(10)11;/h1-4H,5,8H2;1H
SMILES string
Cl.NCc1ccc(cc1)[N+]([O-])=O
assay
97%
form
solid
mp
~265 °C (dec.) (lit.)
solubility
methanol:glacial acetic acid (1:1): soluble 25 mg/mL, clear, colorless to light yellow
functional group
amine, nitro
Quality Level
Application
4-Nitrobenzylamine hydrochloride was used in chemical modification of graphite powder and multiwalled carbon nanotubes. It was also used in the preparation of 2-fluoro-6-(4-nitrohenzylamino)purine.
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
M A Akyüz et al.
Journal of neural transmission (Vienna, Austria : 1996), 114(6), 693-698 (2007-04-03)
Computational studies using the ONIOM methods have been performed to probe the catalytic roles of tyrosine residues 398 and 435 which constitute the "aromatic cage" in the active site of MAO-B. The results presented here provide additional new insights into
The synthesis of a light-switchable amino acid for inclusion into conformationally mobile peptides.
Ulysse L and Chmielewski J.
Bioorganic & Medicinal Chemistry Letters, 4(17), 2145-2146 (1994)
Combinatorial synthesis of 2, 9-substituted purines.
Gray NS, et al.
Tetrahedron Letters, 38(7), 1161-1164 (1997)
A Z Kirkel' et al.
Voprosy meditsinskoi khimii, 32(2), 118-125 (1986-03-01)
Oxidation of p-nitro- and p-dimethylaminomethyl derivatives of benzylamine, catalyzed by amine oxidases from human placenta and blood serum, was studied. The amine oxidase activity was estimated by means of a spectrophotometric procedure involving measurement of aldehyde formed during the reaction
Gaku Fukuhara et al.
Chemical communications (Cambridge, England), 48(11), 1641-1643 (2011-12-15)
Chiral recognition abilities of the title host for (R)- and (S)-α-methyl-4-nitrobenzylamine were examined in the ground and excited states to give a relative affinity (K(R)/K(S)) of 2.16 by spectral titration and a relative rate constant (k(R)/k(S)) of 2.23 by fluorescence
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