| Identification | Back Directory | [Name]
1-(2-Bromoethoxy)-4-nitrobenzene | [CAS]
13288-06-7 | [Synonyms]
NSC 37983 -Bromo-4-nitrophenetole b-Bromo-4-nitrophenetole 4-Nitrophenoxyethylbromide beta-Bromo-4-nitrophenetole p-Nitrophenyl -Bromoethyl Ether 2-(4-Nitrophenoxy)ethyl bromide p-Nitrophenyl b-Bromoethyl Ethe 1-(2-BROMOETHOXY)-4-NITROBENZENE 2-(4-Nitrophenoxy)-1-bromoethane 2-Bromoethyl-4-nitrophenyl Ether 1-(2-Bromoethoxy)-4-nitrobenzene 98% 1-(2-BROMOETHOXY)-4-NITROBENZENE, 98+% 1-(2-BroMoethoxy)-4-nitrobenzene, 98% 5GR 1-(2-BroMoethoxy)-4-nitrobenzene, 98% 25GR 1-(2-Bromoethoxy)-4-nitrobenzene
2-Bromoethyl 4-nitrophenyl Ether | [EINECS(EC#)]
679-539-4 | [Molecular Formula]
C8H8BrNO3 | [MDL Number]
MFCD00031363 | [MOL File]
13288-06-7.mol | [Molecular Weight]
246.06 |
| Chemical Properties | Back Directory | [Appearance]
Off-White Solid | [Melting point ]
62-65 °C
| [Boiling point ]
170 °C / 0.5mmHg | [density ]
1.587±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
Chloroform (Slightly), Dichloromethane (Slightly), DMSO (Slightly), Ethyl Acetat | [form ]
Powder or Crystals | [color ]
Yellow | [InChI]
InChI=1S/C8H8BrNO3/c9-5-6-13-8-3-1-7(2-4-8)10(11)12/h1-4H,5-6H2 | [InChIKey]
YQWCBDNNEZHPMA-UHFFFAOYSA-N | [SMILES]
C1(OCCBr)=CC=C([N+]([O-])=O)C=C1 |
| Hazard Information | Back Directory | [Chemical Properties]
Off-White Solid | [Uses]
1-(2-Bromoethoxy)-4-nitrobenzene serves as the starting material for the synthesis of the bispecific receptor C4TB. It can also be converted into 4-(2-bromoethoxy)aniline via nitro reduction [1]. | [Synthesis Reference(s)]
Synthesis, p. 693, 1972 DOI: 10.1055/s-1972-21970 | [References]
[1]
Reddy, M. B., Shailaja, M., Manjula, A., Premkumar, J. R., Sastry, G. N., Sirisha, K., Sarma, A. V. S. (2015). Design and synthesis of Tröger's base ditopic receptors: host–guest interactions, a combined theoretical and experimental study. Organic & Biomolecular Chemistry, 13(4), 1141–1149. https://doi.org/10.1039/c4ob02266a |
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