2-(p-diethylaminobenzylidene)-1,3-indandione

DOI: 10.1107/S0108270196007457

Source and publish data:

Acta Crystallographica, Section C: Crystal Structure Communications p. 2878 - 2880 (1996)

Update date:2022-08-17

Topics:

Authors:

Khodorkovsky, Vladimir

Mazor, Royi A.

Ellern, Arkady

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1107/S0108270196007457

The title compound, C₂₀H₁₉NO₂, belongs to the class of donor-acceptor-substituted conjugated polyenes. Within the structure, O atoms are situated in the plane of the 1,3-indandione fragment and the N atom lies in the plane of the p-benzylidene fragment which forms a dihedral angle of 7.6 (2)° with the indandione nucleus.

Full text of DOI:10.1107/S0108270196007457

Products guided by the article

Product name:2-[[4-(diethylamino)phenyl]methylene]-1H-indene-1,3(2H)-dione

Cas No:34200-53-8

R&D Labs maybe for 34200-53-8

Xiamen Hisunny Chemical Co.,Ltd

website:http://www.hisunnychem.com

Contact:+86-592-3327115

Address:Unit 603,No.879,Xiahe Road,Meixin Building,Xiamen,China
Chengdu Push Bio-technology Co., Ltd

Contact:86-28-85370565

Address:No.8 Wuke West Second Road, Wuhou
Yurui(Shanghai)Chemical Co.,Ltd

Contact:0086 21-50456736

Address:No.3188 Xiupu Road,Shanghai
Xi'an Galaxy Chemicals CO., Ltd

Contact:86-29-89380370

Address:No.8, Gaoxin three road, Xi'an city.
Hangzhou Haiqiang Chemical Co.,Ltd.

Contact:+86-571-86960370

Address:Add: 5/F, Around Town North Road,No. 10, Hangzhou, Zhejiang,China

Relevant to this article

Doi:10.1038/sj.bjp.0704281
()
Determination of the time course of an enzymatic reaction by ¹H NMR spectroscopy: Hydroxynitrile lyase catalysed transhydrocyanation

Doi:10.1016/0584-8539(95)01574-4
(1996)
Efficient mesoporous silica-titania catalysts from colloidal self-assembly

Doi:10.1039/c2cc35127g
(2012)
Synthetic, structural, NMR, and computational study of a geminally bis(peri-substituted) tridentate phosphine and its chalcogenides and transition-metal complexes

Doi:10.1021/ic3024875
(2013)
Doi:10.1039/F19797502027
()
Absolute configuration of amphidinol 3, the first complete structure determination from amphidinol homologues: Application of a new configuration analysis based on carbon-hydrogen spin-coupling constants [8]

Doi:10.1021/ja983655x
(1999)

Article Doi