1,3-Indandione, 2-(p-dimethylaminobenzylidene)-

Base Information

Chemical Name:1,3-Indandione, 2-(p-dimethylaminobenzylidene)-
CAS No.:21889-13-4
Molecular Formula:C18H15 N O2
Molecular Weight:277.323
Hs Code.:2922399090
NSC Number:636618,86434
UNII:6DK9PDF575
DSSTox Substance ID:DTXSID20176291
Nikkaji Number:J40.991J
ChEMBL ID:CHEMBL1895841
Mol file:21889-13-4.mol

Synonyms:21889-13-4;1,3-Indandione, 2-(p-dimethylaminobenzylidene)-;2-[4-(Dimethylamino)benzylidene]-1,3-indandione;2-[[4-(dimethylamino)phenyl]methylidene]indene-1,3-dione;6DK9PDF575;2-(4-(Dimethylamino)benzylidene)-1H-indene-1,3(2H)-dione;2-[4-(dimethylamino)benzylidene]-1H-indene-1,3(2H)-dione;NSC 86434;NSC-86434;NSC636618;NSC-636618;BRN 2216466;N,N-dimethylaminobenzylidene-1,3-indandione;1H-Indene-1,3(2H)-dione, 2-((4-(dimethylamino)phenyl)methylene)-;2-(4-Dimethylaminobenzylidene)-1,3-indandione;1,3-Indandione, 2-(4-dimethylaminophenylmethylene);1,3-Indandione, 2- (4-dimethylaminophenylmethylene);2-{[4-(dimethylamino)phenyl]methylidene}-2,3-dihydro-1H-indene-1,3-dione;2-(4-(DIMETHYLAMINO)BENZYLIDENE)-1,3-INDANDIONE;NSC86434;DMABI;2-((4-(DIMETHYLAMINO)PHENYL)METHYLENE)INDANE-1,3-DIONE;UNII-6DK9PDF575;F1135-0037;SCHEMBL1454792;CHEMBL1895841;DTXSID20176291;MFCD00184255;STK046510;AKOS001014301;1, 2-(4-dimethylaminophenylmethylene);1, 2-[p-(dimethylamino)benzylidene]-;NCGC00184095-01;NCGC00184095-02;NCGC00184095-03;LS-81176;MS-10746;CS-0300236;2-(p-dimethylaminobenzylidene)-1,3-indanedione;3-14-00-00505 (Beilstein Handbook Reference);AE-641/00595009;SR-01000087535;SR-01000087535-1;2-(P-DIMETHYLAMINOBENZYLIDENE)-1,3-INDANDIONE;2-[(4-dimethylaminophenyl)methylene]indane-1,3-dione;Z44300970;1H-Indene-1, 2-[[4-(dimethylamino)phenyl]methylene]-;1,3-INDANDIONE, 2-(P-(DIMETHYLAMINO)BENZYLIDENE)-;2-(((4-DIMETHYLAMINO)PHENYL)METHYLENE)-1,3-INDANDIONE;2-(4-(N,N-DIMETHYLAMINO)BENZILIDENE)INDANE-1,3-DIONE;2-((4-(DIMETHYLAMINO)PHENYL)METHYLENE)-1H-INDENE-1,3(2H)-DIONE;2-(4-(N,N-DIMETHYLAMINO)BENZYLIDENE)-1H-INDENE-1,3(2H)-DIONE

Suppliers and Price of 1,3-Indandione, 2-(p-dimethylaminobenzylidene)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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Total 7 raw suppliers

Chemical Property of 1,3-Indandione, 2-(p-dimethylaminobenzylidene)-

Chemical Property:

Vapor Pressure:7.78E-10mmHg at 25°C
Boiling Point:492.3°Cat760mmHg
Flash Point:231.7°C
PSA：37.38000
Density:1.276g/cm³
LogP:3.21520
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:277.110278721
Heavy Atom Count:21
Complexity:432

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)C1=CC=C(C=C1)C=C2C(=O)C3=CC=CC=C3C2=O
General Description 1,3-Indandione, 2-(4-dimethylaminophenylmethylene) (DMABI) is a derivative of 2-arylidene-indan-1,3-dione, exhibiting a push-pull (D-π-A) structure due to its electron-donating dimethylamino group and electron-accepting indandione core. 1,3-Indandione, 2- (4-dimethylaminophenylmethylene) has potential applications in photopolymerization as a visible-light photoinitiator, given its ability to absorb a broad spectrum of light (blue-to-red). Additionally, its structural framework suggests possible biological activity, including anti-cancer, antiviral, or antibacterial properties, though specific data on this derivative may require further investigation. Its synthesis typically involves Knoevenagel condensation, highlighting its role as a versatile chromophore in materials science and medicinal chemistry.

Technology Process of 1,3-Indandione, 2-(p-dimethylaminobenzylidene)-

There total 4 articles about 1,3-Indandione, 2-(p-dimethylaminobenzylidene)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.0%