julolidine

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| 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

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}}

Julolidine is a heterocyclic aromatic organic compound. It has the formula C12H15N.

Synthesis

The first synthesis of julolidine was first reported by G. Pinkus in 1892.Pinkus, G. Ueber die Einwirkung von Trimethylenchlorbromid auf einige aromatische Amine und Amide. Berichte der deutschen chemischen Gesellschaft 1892, 25 (2), 2798–2806

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

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