184802
4-Nitrophenethylamine hydrochloride
95%
Synonym(s):
2-(4-Nitrophenyl)ethylamine hydrochloride
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About This Item
Linear Formula:
O2NC6H4CH2CH2NH2 · HCl
CAS Number:
Molecular Weight:
202.64
Beilstein:
3568915
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
95%
form
solid
mp
200 °C (dec.) (lit.)
functional group
amine
nitro
SMILES string
Cl.NCCc1ccc(cc1)[N+]([O-])=O
InChI
1S/C8H10N2O2.ClH/c9-6-5-7-1-3-8(4-2-7)10(11)12;/h1-4H,5-6,9H2;1H
InChI key
JVMHULJEYUQYSH-UHFFFAOYSA-N
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Related Categories
Application
4-Nitrophenethylamine hydrochloride was used in the synthesis of:
- ortho-metalated primary phenethylamines complexes containing six-membered palladacycles
- N-(4-nitrophenethyl)formamide
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
Regulatory Information
监管及禁止进口产品
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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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