julolidine
{{chembox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 459434931
| ImageFile = Julolidine.png
| ImageFile_Ref = {{Chemboximage|correct|??}}
| ImageName = Diagram showing structure of julolidine
| PIN = 2,3,6,7-Tetrahydro-1H,5H-pyrido[3,2,1-ij]quinoline
| OtherNames =
|Section1={{Chembox Identifiers
| CASNo = 479-59-4
| CASNo_Ref = {{cascite|correct|CAS}}
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 8ERL3KJ6GQ
| PubChem = 68069
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 61383
| SMILES = c13c2c(ccc1)CCCN2CCC3
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C12H15N/c1-4-10-6-2-8-13-9-3-7-11(5-1)12(10)13/h1,4-5H,2-3,6-9H2
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = DZFWNZJKBJOGFQ-UHFFFAOYSA-N
}}
|Section2={{Chembox Properties
| C=12 | H=15 | N=1
| Appearance =
| Density = 1.003 g/mL
| MeltingPtC = 35
| BoilingPt =
| RefractIndex = 1.568
}}
|Section7={{Chembox Hazards
| FlashPtC = 110
}}
}}
Julolidine is a heterocyclic aromatic organic compound. It has the formula C12H15N.
Synthesis
Applications
This compound and its derivatives have found recent interest as photoconductive materials, chemiluminescence
substances, chromogenic substrates in analytical redox reactions, dye intermediates, potential antidepressants
and tranquilizers, nonlinear optical materials, high sensitivity photopolymerizable materials, and for improving color stability in photography.
References
{{reflist}}
External links
- {{cite journal | doi = 10.1021/jo9519118| pmid = 11667174| title = Convenient Synthesis of Julolidines Using Benzotriazole Methodology| journal = The Journal of Organic Chemistry| volume = 61| issue = 9| pages = 3117| year = 1996| last1 = Katritzky| first1 = Alan R.| last2 = Rachwal| first2 = Bogumila| last3 = Rachwal| first3 = Stanislaw| last4 = Abboud| first4 = Khalil A.}}