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derivatives, the diamine converts to phthaloperinones. The derivative from phthalic anhydride itself, Solvent Orange 60, is a useful orange pigment. It is a precursor to
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It is prepared by reduction of 1,8-dinitronaphthalene, which in turn is obtained as a mixture of isomers by nitration of 1-nitronaphthalene.
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448:. It is a colorless solid that darkens in air due to oxidation. It is a precursor to commercial pigments.
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545:"Green Synthesis of Polycyclic Benzimidazole Derivatives and Organic Semiconductors"
592:"A new catalyst for the synthesis of 2-substituted perimidines catalysed by FePO4"
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Chemical structure of 12-phthaloperinone, a derivative of 1,8-diaminonaphthalene
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Except where otherwise noted, data are given for materials in their
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Mamada, Masashi; PéRez-BolíVar, César; Anzenbacher, Pavel (2011).
475:. This compound used to produce perimidines by various aldehydes.
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InChI=1S/C10H10N2/c11-8-5-1-3-7-4-2-6-9(12)10(7)8/h1-6H,11-12H2
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InChI=1/C10H10N2/c11-8-5-1-3-7-4-2-6-9(12)10(7)8/h1-6H,11-12H2
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515:Booth, Gerald (2005). "Naphthalene Derivatives".
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267:Key: YFOOEYJGMMJJLS-UHFFFAOYSA-N
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590:F.K. Behbahani, F.M.Golchin (2017).
277:Key: YFOOEYJGMMJJLS-UHFFFAOYAU
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473:1,8-bis(dimethylamino)naphthalene
369:1,8-bis(dimethylamino)naphthalene
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50:Deltamin, 1,8-Naphthalenediamine
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380:(at 25 °C , 100 kPa).
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620:10.1016/j.jtusci.2015.10.004
298:C1=CC2=C(C(=C1)N)C(=CC=C2)N
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441:. It is one of several
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452:Synthesis and reactions
41:Naphthalene-1,8-diamine
17:1,8-Diaminonaphthalene
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419:1,8-Diaminonaphthalene
346:158.1998
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467:Upon treatment with
303:c1(cccc2cccc(N)c12)N
37:Preferred IUPAC name
611:2017JTUS...11...85B
446:naphthalenediamines
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469:phthalic anhydride
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425:with the formula C
407:Infobox references
351:Related compounds
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561:10.1021/ol201973w
555:(18): 4882–4885.
415:Chemical compound
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220:CompTox Dashboard
104:Interactive image
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124:ChEMBL595537
56:Identifiers
48:Other names
312:Properties
162:100.006.846
643:Categories
502:References
342:Molar mass
208:IKA7029YH9
135:ChemSpider
84:3D model (
63:CAS Number
654:Diamines
629:98648448
577:32185653
569:21863817
479:See also
443:isomeric
357:Related
73:479-27-6
607:Bibcode
400:what is
398: (
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175:PubChem
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421:is an
395:verify
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291:SMILES
115:ChEMBL
31:Names
625:S2CID
595:(PDF)
573:S2CID
256:InChI
188:68067
144:61381
86:JSmol
565:PMID
523:ISBN
199:UNII
615:doi
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433:(NH
225:EPA
178:CID
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493:N
489:H
485:C
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429:H
390:N
334:2
332:N
328:H
324:C
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223:(
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