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191663
3-Nitrobenzylamin -hydrochlorid
97%
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Lineare Formel:
O2NC6H4CH2NH2 · HCl
CAS-Nummer:
Molekulargewicht:
188.61
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
247-502-8
MDL number:
Assay:
97%
Form:
solid
assay
97%
form
solid
mp
229-231 °C (lit.)
functional group
amine, nitro
SMILES string
Cl.NCc1cccc(c1)[N+]([O-])=O
InChI
1S/C7H8N2O2.ClH/c8-5-6-2-1-3-7(4-6)9(10)11;/h1-4H,5,8H2;1H
InChI key
DLZXLCHQWOZGSE-UHFFFAOYSA-N
Application
3-Nitrobenzylamine hydrochloride was used in the synthesis of an azobenzene amino acid used as photo-inducible conformational switch in polypeptides[1]. It was also used in the synthesis of 2,4-dimethoxybenzylidene-3-nitrobenzylamine.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Lagerklasse
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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X= Y-ZH Systems as Potential 1, 3-Dipoles. Part 45.1, 2Proton Sponge Effects on the 1, 2-Prototropic Formation of Azomethine Ylides from Arylidene Benzylamines.
Grigg R, et al.
Tetrahedron, 51(48), 13331-13346 (1995)
Andreas Aemissegger et al.
Nature protocols, 2(1), 161-167 (2007-04-03)
The synthesis of an azobenzene amino acid (aa) for use as a photo-inducible conformational switch in polypeptides is described. The compound can be easily incorporated into an aa sequence by solid-phase peptide synthesis using standard 9-fluorenylmethoxycarbonyl methods. A reversible conformational
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 191663-1G | 04061825763071 |
| 191663-5G | 04061832098630 |