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rings. Relative to the properties of ferrocene, its melting point is lower and its solubility of the compound in
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It was once used as an additive in rocket propellant, to promote the burning rate. It can be synthesized by the
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InChI=1S/C7H9.C5H5.Fe/c1-2-7-5-3-4-6-7;1-2-4-5-3-1;/h3-6H,2H2,1H3;1-5H;
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Except where otherwise noted, data are given for materials in their
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81 to 86 °C (178 to 187 °F; 354 to 359 K)
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414:containing an ethyl group on one of the two
458:. Watson International Ltd. Archived from
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327:264 °C (507 °F; 537 K)
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220:Key: XEYMPZDIHJESAH-UHFFFAOYSA-N
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486:Selected Works in Organic Chemistry
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494:10.1016/b978-0-08-010158-3.50085-8
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337:(at 25 °C , 100 kPa).
488:, Elsevier, pp. 665–668,
482:"Synthesis of Alkylferrocenes"
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480:Vol'Kenau, N.A. (1963),
410:. It is a derivative of
422:solvents is improved.
241:.1(CC)C=CC=C1.1C=CC=C1
432:Clemmensen reduction
37:Preferred IUPAC name
426:Use and preparation
380:organoiron compound
289: g·mol
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364:Infobox references
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503:978-0-08-010158-3
382:with the formula
372:Chemical compound
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173:CompTox Dashboard
97:Interactive image
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456:"Ethylferrocene"
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416:cyclopentadienyl
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257:Chemical formula
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436:acetylferrocene
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359: ?)
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297:Dark brown oil
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17:Ethylferrocene
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376:Ethylferrocene
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190:DTXSID60925841
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50:Ethylferrocene
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462:on 2012-04-02
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129:ECHA InfoCard
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507:, retrieved
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464:. Retrieved
460:the original
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56:Identifiers
48:Other names
420:hydrocarbon
307:1.256 g/mL
294:Appearance
250:Properties
135:100.013.688
529:Ferrocenes
509:2021-11-03
466:2012-08-06
442:References
282:Molar mass
108:ChemSpider
84:3D model (
63:CAS Number
412:ferrocene
73:1273-89-8
523:Category
161:16213263
117:24767649
357:what is
355: (
303:Density
287:214.089
148:PubChem
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378:is an
352:verify
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234:SMILES
31:Names
209:InChI
86:JSmol
498:ISBN
384:Fe(C
490:doi
434:of
178:EPA
151:CID
525::
496:,
484:,
438:.
392:)C
275:Fe
272:14
266:12
492::
469:.
408:)
406:5
404:H
402:2
400:C
398:4
396:H
394:5
390:5
388:H
386:5
347:Y
269:H
263:C
180:)
176:(
88:)
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