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InChI=1S/C36H32Cl4N6O4/c1-17-7-9-29(19(3)11-17)41-35(49)33(21(5)47)45-43-31-15-25(37)23(13-27(31)39)24-14-28(40)32(16-26(24)38)44-46-34(22(6)48)36(50)42-30-10-8-18(2)12-20(30)4/h7-16,33-34H,1-6H3,(H,41,49)(H,42,50)/b45-43+,46-44+
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Cc1cc(C)ccc1NC(=O)C(C(=O)C)/N=N/c2cc(Cl)c(cc2Cl)-c3cc(Cl)c(cc3Cl)/N=N/C(C(=O)C)C(=O)Nc4ccc(C)cc4C
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Except where otherwise noted, data are given for materials in their
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The compound is synthesized from three components. Treatment of
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373:aniline. This compound is then coupled to the bis
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38:Benzidine Yellow 10G, Sanyo Pigment Yellow 8105
398:Ullmann's Encyclopedia of Industrial Chemistry
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396:K. Hunger. W. Herbst "Pigments, Organic" in
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246:Key: GPWXTTPSHZOIKO-MWOVFPFUSA-N
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362:. It is used as a yellow colorant.
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336:(at 25 °C , 100 kPa).
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400:, Wiley-VCH, Weinheim, 2012.
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406:10.1002/14356007.a20_371
358:that is classified as a
369:with diketene gives an
379:3,3'-dichlorobenzidine
318:754.49
367:2,4-dimethylaniline
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438:Diarylide pigments
340:Infobox references
17:Pigment Yellow 81
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360:diarylide pigment
352:Pigment Yellow 81
348:Chemical compound
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199:CompTox Dashboard
85:Interactive image
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433:Shades of yellow
428:Organic pigments
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356:organic compound
283:Chemical formula
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371:acetoacetylated
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375:diazonium salt
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44:Identifiers
36:Other names
323:Appearance
276:Properties
123:100.040.691
417:Categories
385:References
314:Molar mass
187:DGH1X24C9Z
96:ChemSpider
72:3D model (
61:22094-93-5
51:CAS Number
144:244-776-0
136:EC Number
423:Pigments
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154:PubChem
354:is an
260:SMILES
31:Names
235:InChI
167:89597
105:80866
74:JSmol
178:UNII
402:doi
204:EPA
157:CID
419::
381:.
296:Cl
294:32
290:36
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306:4
304:O
302:6
300:N
298:4
292:H
288:C
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202:(
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