184802
4-硝基苯乙胺 盐酸盐
95%
别名:
2-(4-硝基苯基)乙胺 盐酸盐
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关于此项目
线性分子式:
O2NC6H4CH2CH2NH2 · HCl
化学文摘社编号:
分子量:
202.64
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
249-980-3
Beilstein/REAXYS Number:
3568915
MDL number:
产品名称
4-硝基苯乙胺 盐酸盐, 95%
InChI key
JVMHULJEYUQYSH-UHFFFAOYSA-N
InChI
1S/C8H10N2O2.ClH/c9-6-5-7-1-3-8(4-2-7)10(11)12;/h1-4H,5-6,9H2;1H
SMILES string
Cl.NCCc1ccc(cc1)[N+]([O-])=O
assay
95%
form
solid
mp
200 °C (dec.) (lit.)
functional group
amine
nitro
Quality Level
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Application
4-Nitrophenethylamine hydrochloride was used in the synthesis of:
- ortho-metalated primary phenethylamines complexes containing six-membered palladacycles
- N-(4-nitrophenethyl)formamide
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)
法规信息
监管及禁止进口产品
此项目有
Li-Ping He et al.
Acta crystallographica. Section E, Structure reports online, 66(Pt 7), o1721-o1721 (2010-01-01)
The title compound, C(9)H(10)N(2)O(3), was synthesized by direct N-formyl-ation of 4-nitro-phenethyl-amine hydro-chloride with formic acid and sodium formate in the absence of catalyst and solvent. In the crystal structure, mol-ecules are linked by inter-molecular N-H⋯O hydrogen-bond inter-actions into chains parallel
Ortho-metalated primary amines. 6.1 The first synthesis of six-membered palladacycles from primary amines containing electron-withdrawing substituents: end of the limiting rules of Cope and Friedrich on cyclopalladation of benzyl-and phenethylamines.
Vicente J, et al.
Organometallics, 22(26), 5513-5517 (2003)
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