(E)-2-(2-Nitroethenyl)furan
The title compound, C6H5NO3, was synthesized via condensation of furfural with nitromethane in the presence of isobutylamine. The compound crystallizes exclusively as the E isomer. The angle between the mean planes of the furan ring and the nitroalkenyl group is 1.3 (2)°.
| Main Authors: | , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
International Union of Crystallography
2009-08-01
|
| Series: | Acta Crystallographica Section E |
| Online Access: | http://scripts.iucr.org/cgi-bin/paper?S160053680902861X |
| _version_ | 1819281312216776704 |
|---|---|
| author | Pedro Valerga M. Carmen Puerta Zenaida Rodríguez Negrín Nilo Castañedo Cancio Miguel Palma Lovillo |
| author_facet | Pedro Valerga M. Carmen Puerta Zenaida Rodríguez Negrín Nilo Castañedo Cancio Miguel Palma Lovillo |
| author_sort | Pedro Valerga |
| collection | DOAJ |
| description | The title compound, C6H5NO3, was synthesized via condensation of furfural with nitromethane in the presence of isobutylamine. The compound crystallizes exclusively as the E isomer. The angle between the mean planes of the furan ring and the nitroalkenyl group is 1.3 (2)°. |
| first_indexed | 2024-12-24T00:57:41Z |
| format | Article |
| id | doaj.art-53fa3b0c797f4d4882850042dce5b7d5 |
| institution | Directory Open Access Journal |
| issn | 1600-5368 |
| language | English |
| last_indexed | 2024-12-24T00:57:41Z |
| publishDate | 2009-08-01 |
| publisher | International Union of Crystallography |
| record_format | Article |
| series | Acta Crystallographica Section E |
| spelling | doaj.art-53fa3b0c797f4d4882850042dce5b7d52022-12-21T17:23:26ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682009-08-01658o1979o197910.1107/S160053680902861X(E)-2-(2-Nitroethenyl)furanPedro ValergaM. Carmen PuertaZenaida Rodríguez NegrínNilo Castañedo CancioMiguel Palma LovilloThe title compound, C6H5NO3, was synthesized via condensation of furfural with nitromethane in the presence of isobutylamine. The compound crystallizes exclusively as the E isomer. The angle between the mean planes of the furan ring and the nitroalkenyl group is 1.3 (2)°.http://scripts.iucr.org/cgi-bin/paper?S160053680902861X |
| spellingShingle | Pedro Valerga M. Carmen Puerta Zenaida Rodríguez Negrín Nilo Castañedo Cancio Miguel Palma Lovillo (E)-2-(2-Nitroethenyl)furan Acta Crystallographica Section E |
| title | (E)-2-(2-Nitroethenyl)furan |
| title_full | (E)-2-(2-Nitroethenyl)furan |
| title_fullStr | (E)-2-(2-Nitroethenyl)furan |
| title_full_unstemmed | (E)-2-(2-Nitroethenyl)furan |
| title_short | (E)-2-(2-Nitroethenyl)furan |
| title_sort | e 2 2 nitroethenyl furan |
| url | http://scripts.iucr.org/cgi-bin/paper?S160053680902861X |
| work_keys_str_mv | AT pedrovalerga e22nitroethenylfuran AT mcarmenpuerta e22nitroethenylfuran AT zenaidarodramp237gueznegramp237n e22nitroethenylfuran AT nilocastaamp241edocancio e22nitroethenylfuran AT miguelpalmalovillo e22nitroethenylfuran |