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Collin, Gerd; Mildenberg, Rolf; Zander, Mechthild; Höke, Hartmut; McKillip, William; Freitag, Werner; Imöhl, Wolfgang (2000). "Resins, Synthetic".
962:
1081:
1097:
O'Connor, Joseph M.; Casey, Charles P. (1987). "Ring-Slippage
Chemistry of Transition Metal Cyclopentadienyl and Indenyl Complexes".
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liquid is colorless although samples often are pale yellow. The principal industrial use of indene is in the production of indene/
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by sodium to give the indenyl derivative. The sodio-indene is converted back to indene by steam
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to precipitate solid "sodio-indene". This step exploits indene's weak acidity evidenced by its
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Wu, Jie; Qiu, Guanyinsheng (2014). "Generation of Indene
Derivatives by Tandem Reactions".
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Nomenclature of
Organic Chemistry: IUPAC Recommendations and Preferred Names 2013
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boiling around 175–185 °C. It can be obtained by heating this fraction with
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Bordwell FG (1988). "Equilibrium acidities in dimethyl sulfoxide solution".
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thermoplastic resins. Substituted indenes and their closely related
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Except where otherwise noted, data are given for materials in their
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derivatives are important structural motifs found in many
820:-carboxylphenylacetic acid). It condenses with diethyl
685:
844:, which are highly coloured. Treatment of indene with
991:
National
Institute for Occupational Safety and Health
939:International Union of Pure and Applied Chemistry
312:
102:
27:Bicyclic hydrocarbon compound with formula C9H8
1158:Berichte der Deutschen Chemischen Gesellschaft
1133:Berichte der Deutschen Chemischen Gesellschaft
1073:Ullmann's Encyclopedia of Industrial Chemistry
390:InChI=1S/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2
400:InChI=1/C9H8/c1-2-5-9-7-3-6-8(9)4-1/h1-6H,7H2
8:
503:181.6 °C (358.9 °F; 454.8 K)
587:78.3 °C (172.9 °F; 351.4 K)
493:−1.8 °C (28.8 °F; 271.3 K)
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1181:. Longman Scientific & Technical.
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828:to form indene–oxalic ester, and with
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393:Key: YBYIRNPNPLQARY-UHFFFAOYSA-N
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403:Key: YBYIRNPNPLQARY-UHFFFAOYAJ
303:
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888:transition metal indenyl complexes
25:
1154:"Zur Synthese von Indenderivaten"
1129:"Zur Synthese von Indenderivaten"
808:. Oxidation of indene with acid
675:
45:
36:
671:(at 25 °C , 100 kPa).
623:TWA 10 ppm (45 mg/m)
947:The Royal Society of Chemistry
564:Occupational safety and health
1:
1007:Accounts of Chemical Research
597:(US health exposure limits):
1152:W. v. Miller, Rohde (1890).
1127:W. v. Miller, Rohde (1890).
81:Bicyclonona-1,3,5,7-tetraene
777:Indene occurs naturally in
1222:
1025:Bordwell pKa Table in DMSO
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1170:10.1002/cber.18900230228
1145:10.1002/cber.18900230227
884:organometallic chemistry
1076:. Weinheim: Wiley-VCH.
848:reagents gives lithium
734:. It is composed of a
540:Magnetic susceptibility
1057:10.1055/s-0034-1379318
886:, giving rise to many
1177:Finar, I. L. (1985).
955:10.1039/9781849733069
465:116.16
77:Benzocyclopentadiene
60:Preferred IUPAC name
1111:10.1021/cr00078a002
1020:10.1021/ar00156a004
836:in the presence of
824:in the presence of
765:molecules, such as
763:biologically active
510:Solubility in water
140:Beilstein Reference
32:
1030:2008-10-09 at the
698:Infobox references
641:Related compounds
632:(Immediate danger)
30:
1179:Organic Chemistry
1051:(19): 2703–2713.
964:978-0-85404-182-4
814:homophthalic acid
706:Chemical compound
704:
703:
647:Related compounds
473:Colorless liquid
346:CompTox Dashboard
128:Interactive image
16:(Redirected from
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424:c1ccc2c(c1)CC=C2
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79:Indonaphthene
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794:distillation
776:
745:ring. This
743:cyclopentene
709:
708:
593:
573:Main hazards
562:
524:
180:ChEMBL192812
87:Identifiers
75:Other names
65:
865:+ RLi → LiC
852:compounds:
806:polymerises
718:hydrocarbon
583:Flash point
567:(OHS/OSH):
483:0.997 g/mL
470:Appearance
433:Properties
238:100.002.176
160:CHEBI:41921
926:References
810:dichromate
800:Reactivity
652:Benzofuran
577:Flammable
515:Insoluble
461:Molar mass
334:67H8Y6LB8A
191:ChemSpider
115:3D model (
94:CAS Number
910:Isoindene
830:aldehydes
782:fractions
773:Isolation
751:coumarone
747:flammable
259:202-393-6
251:EC Number
1200:Category
1028:Archived
993:(NIOSH).
941:(2014).
920:Indenone
894:See also
840:to form
779:coal-tar
767:sulindac
714:aromatic
557:Hazards
542:(χ)
211:DrugBank
1206:Indenes
1045:Synlett
987:"#0340"
850:indenyl
834:ketones
822:oxalate
812:yields
736:benzene
691:what is
689: (
521:Acidity
479:Density
455:
301:PubChem
220:DB02815
145:635873
104:95-13-6
68:-Indene
31:Indene
18:Indenes
1185:
1080:
961:
905:Indole
900:Indane
880:ligand
838:alkali
786:sodium
755:indane
712:is an
710:Indene
686:verify
683:
660:Indole
547:−80.89
417:SMILES
289:C11565
274:27265
171:ChEMBL
54:Names
720:with
636:N.D.
610:none
594:NIOSH
382:InChI
151:ChEBI
117:JSmol
1183:ISBN
1078:ISBN
959:ISBN
873:+ RH
761:and
739:ring
630:IDLH
325:UNII
314:7219
280:KEGG
200:6949
1166:doi
1141:doi
1107:doi
1053:doi
1016:doi
951:doi
882:in
832:or
617:REL
604:PEL
351:EPA
304:CID
1202::
1162:23
1160:.
1156:.
1137:23
1135:.
1131:.
1103:87
1101:.
1049:25
1047:.
1012:21
1010:.
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973:^
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523:(p
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967:.
953::
871:7
869:H
867:9
863:8
861:H
859:9
857:C
818:o
816:(
731:8
729:H
727:9
725:C
681:Y
549:×
528:a
525:K
452:8
450:H
448:9
446:C
353:)
349:(
119:)
66:H
64:1
20:)
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