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Merck
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Documenti

P73005

Sigma-Aldrich

Pyromellitic diimide

97%

Sinonimo/i:

Benzene-1,2,4,5-tetracarboxylic diimide, Reillex® 402

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About This Item

Formula empirica (notazione di Hill):
C10H4N2O4
Numero CAS:
2550-73-4
Peso molecolare:
216.15
Beilstein:
214780
Numero CE:
219-852-1
Numero MDL:
MFCD00005004
Codice UNSPSC:
12352100
ID PubChem:
24898838
NACRES:
NA.22

Saggio

97%

Forma fisica

powder

Punto di fusione

>320 °C (lit.)

Stringa SMILE

O=C1NC(=O)c2cc3C(=O)NC(=O)c3cc12

InChI

1S/C10H4N2O4/c13-7-3-1-4-6(10(16)12-8(4)14)2-5(3)9(15)11-7/h1-2H,(H,11,13,15)(H,12,14,16)
UGQZLDXDWSPAOM-UHFFFAOYSA-N

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Categorie correlate

Note legali

Reillex is a registered trademark of Vertellus Specialties, Inc.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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S A Martin et al.
Journal of animal science, 60(2), 544-550 (1985-02-01)
The effects of monensin, 2-bromoethanesulfonic acid (2-BES) and pyromellitic diimide (diimide) on gas and volatile fatty acid (VFA) production by the rumen microbiota were compared in mixed culture. Oat hay, a hay-concentrate mixture (48% hay, 43% concentrate) and a soluble
Rocío García-Bueno et al.
Dalton transactions (Cambridge, England : 2003), 39(24), 5728-5736 (2010-05-25)
The hydroxo-complexes [Ni(2)(mcN(3))(2)(mu-OH)](2)(PF(6))(2)] [mcN(3) = 2,4,4-trimethyl-1,5,9-triazacyclododec-1-ene (Me(3)-mcN(3)) or 2,4,4,9-tetramethyl-1,5,9-triazacyclododec-1-ene (Me(4)-mcN(3))] react with imides (Him) in 1 : 2 (succinimide, glutarimide, saccharine and 1,8-naphthalimide) or 1 : 1 (pyromellitic diimide) molar ratio, leading to the formation of the imidate complexes: [Ni(mcN(3))(H(2)O)(Im)](+)
Shin-ichiro Kato et al.
The Journal of organic chemistry, 71(13), 4723-4733 (2006-06-17)
This paper reports the electroscopic and electrochemical properties of [2 + 2] pyromellitic diimide-based cyclophane 1 as well as acyclic N,N'-bis(2-methoxybenzyl)pyromellitic diimide 2 and the clathrate compounds formed by 1. Compound 1 was synthesized by direct cyclocondensation. Its structure was
Bijitha Balan et al.
Organic letters, 9(14), 2709-2712 (2007-06-07)
Complex formation of pyromellitic diimide derivatives with beta-cyclodextrin and anthracene-appended beta-cyclodextrin was studied with use of induced circular dichroism and 1H NMR spectroscopies. It is revealed that pyromellitic diimides form rim-binding type complexes with beta-CD and in these complexes the
Meisa S Khoshbin et al.
Chemistry, an Asian journal, 1(5), 686-692 (2007-04-19)
Pyromellitic diimide and naphthalene diimide moieties were incorporated into hemilabile phosphanylalkyl thioether ligands. These ligands reacted with [Cu(CH3CN)4]PF6 and [Rh(NBD)Cl]2 (NBD = norbornadiene) by the weak-link approach to form condensed intermediates. Upon reaction of each diimide ligand with these transition-metal
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