ProName: Anthracene-maleic anhydride diels-alde CasNo: 5443-16-3; Molecular Formula: C18H12O3; Appearance: ask; Application: intermediates; DeliveryTime: Within 3 days after payment; PackAge: foil aluminium bag/vacuum packing; Port: shanghai; ProductionCapacity: 100 Kilogram/Week; Purity: 85.0-99.8%; Storage: Keep in dry and cool condition

Results 1 - 18 of 18 Anthracene, 2,5-furandione adduct. Anthracene,maleic anhydride adduct. Anthracene-maleic anhydride diels-alder adduct. Endo-9

1992-02-01 · The standard molar enthalpy of combustion of the (anthracene + maleic anhydride) adduct at p o = 0.1 MPa was determined to be Δ c H m o (C 18 H 12 O 3, cr, 298.15 K) = −(8380.0±5.9) kJ·mol −1. The molar enthalpy of fusion of this adduct at its melting temperature (534.07 K), as measured by a 910 DuPont d.s.c. and a 9900 DuPont thermal (analyzer + digital computer), was found to be (36.3 Organic Chemistry II Lab Diels Alder Reaction Purpose: In this experiment a Diels-Alder reaction was used to form the products. Cyclopentadiene and maleic anhydride were reacted together to form cis-Norbornene-5,6-endo-dicarboxylic anhydride. 7-oxabicyclo{2.2.1}hept-5-ene-2,3-dicarboxylic anhydride was also produced through a Diels-Alder reaction with the combination of furan and maleic In the present experimental work, the energy of combustion of the crystalline Diels-Alder adduct of anthracene and maleic anhydride: C18H12O3, was measured with a model 1241 Parr automatic Anthracene-maleic anhydride diels-alder adduct 5443-16-3 Suppliers,provide Anthracene-maleic anhydride diels-alder adduct 5443-16-3 product and the products related with China (Mainland) Anthracene-maleic anhydride diels-alder adduct 5443-16-3 Career Henan Chemical Co China (Mainland) Anthracene-maleic anhydride diels-alder adduct structure data file available for download. It can be imported to most of the chemistry software for further analysis. Obtain SDF at Mol-Instincts.

And Other Advent Substance record SID 341690678 for cis-9,10-dihydro-9,10-ethanoanthracene-11,12-dicarboxylic acid anhydride submitted by Springer Nature. Scheme 1. Synthesis of N-octylmaleimide Diels–Alder adducts of anthracene and a derivative. Scheme 2.

Anthracene, 2,5-furandione adduct. 17-oxapentacyclo[6.6.5.0~2,7~.0~9,14 Other names: Anthracene, 2,5-furandione adduct; Anthracene,maleic anhydride adduct; endo-9,10-(α,β-Succinic anhydride)anthracene; 9,10(3',4')-Furanoanthracene-12,14-dione; 9,10-Dihydroanthraceno-9,10-endo-α,β-succinic anhydride; 9,10-Ethanoanthracene-11,12-dicarboxylic anhydride Permanent link for this species. Use this link for bookmarking Find more compounds similar to Anthracene-maleic anhydride diels-alder adduct.

In the present experimental work, the energy of combustion of the crystalline Diels-Alder adduct of anthracene and maleic anhydride: C18H12O3, was measured with a model 1241 Parr automatic calorimeter and a Parr model 1710 calorimeter controller. The standard molar enthalpy of combustion of the (anthracene + maleic anhydride) adduct at po = 0.1 MPa was determined to be ΔcHmo(C18H12O3, …

Tabulate 3-5 relevant IR peaks for the Diels–Alder reaction product. Compare and contrast the IR spectra of your starting materials (anthracene and maleic anhydride) and product (9,10-dihydroanthracene-9,10-a,b-succinic anhydride) and explain how the IR data for the product confirms the formation of the Diels-Alder adduct. Scheme 1.

Experiment performed on February 25 and 27, 2003. Abstract: This experiment involved a reaction between anthracene and maleic anhydride via a Diels Alder reaction to yield 9, 10-dihydroanthracene-9,10-α, β-succinic anhydride. Anthracene was the diene and maleic anhydride was the dienophile. The percent yield of the crude product was 69.03%.

Anthracene-maleic anhydride diels-alder adduct

and a 9900 DuPont thermal (analyzer + digital computer), was found to be (36.3 Organic Chemistry II Lab Diels Alder Reaction Purpose: In this experiment a Diels-Alder reaction was used to form the products. Cyclopentadiene and maleic anhydride were reacted together to form cis-Norbornene-5,6-endo-dicarboxylic anhydride.

Synthesis of maleic anhydride Diels–Alder adducts of anthracene. Figure 1. A representation of the molecular structure of 1 and 2. Ellipsoids correspond to 50% probability level. S. K. Ayer et al. Tabulate 3-5 relevant IR peaks for the Diels–Alder reaction product. Compare and contrast the IR spectra of your starting materials (anthracene and maleic anhydride) and product (9,10-dihydroanthracene-9,10-a,b-succinic anhydride) and explain how the IR data for the product confirms the formation of the Diels-Alder adduct.
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(diene) maleic anhydride. (dienophile). The reaction is carried lective thermal Diels–Alder reaction, employing maleic anhydride as the dienophile.

Xylene 3 Mar 2013 The Diels-Alder Reaction of Anthracene with Maleic Anhydride - Lu Le Laboratory · This Diels-Alder reaction is carried out by boiling the reactants 25 Sep 2015 In general, Diels - Alder reaction can be represented as: higher for rigid dienophiles such as maleic anhydride and benzoquinone; for others, E- and Z- dienophiles, for example, give rise to the adducts with corresp 40 mM of initial concentrations, precipitation of the polymeric adduct gradually L.; Sumerlin, B. S., Dynamic-covalent nanostructures prepared by Diels-Alder reactions of styrene-maleic anhydride-derived copolymers obtained by one-step. Rosin modified with fumaric acid or maleic anhydride is often used in paper size. in both and was actually the dominating Diels-Alder adduct in one of these.
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The Diels-Alder Reactionof Anthracene withMaleic Anhydrideprepared by L. G. Wade, Jr., Whitman College. Use the Diels-Alder reaction to form a bridged polycyclic anhydride.Recrystallize the product and characterize it by using melting point andinfrared spectroscopy.

1H NMR Spectra of the Diels-Alder Adduct from anthracene and maleic anhydride. The possibility that the Diels-Alder adduct may form by reaction of the properties of the anthracene and maleic anhydride adduct derived from those measured The Diels-Alder reaction between cyclopentadiene and maleic anhydride can produce two possible products, the 'endo' and the 'exo' adducts. This is because Effect of 9- and 10-substituents on the reactivity of anthracene in the. Diels-Alder reaction has been studied by Biermann and Schmidt and it is found that in SYNT 717: The Diels-Alder Reaction of Anthracene with Maleic Anhydride ( adduct) anthracene.

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Anthracene-maleic anhydride diels-alder adduct contains total 33 atom(s); 12 Hydrogen atom(s), 18 Carbon atom(s) and 3 Oxygen atom(s). Learn more about Anthracene-maleic anhydride diels-alder adduct molecular weight at Mol-Instincts.

The expec 6 Nov 2020 Anthracenes typically undergo Diels-Alder reactions or electrophilic substitutions at (a) Inherent reactivity of anthracene with dienophiles.

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Anthracene-maleic anhydride diels-alder adduct 5443-16-3 Suppliers,provide Anthracene-maleic anhydride diels-alder adduct 5443-16-3 product and the products related with China (Mainland) Anthracene-maleic anhydride diels-alder adduct 5443-16-3 Career Henan Chemical Co China (Mainland) In the present experimental work, the energy of combustion of the crystalline Diels-Alder adduct of anthracene and maleic anhydride: C18H12O3, was measured with a model 1241 Parr automatic In the present experimental work, the energy of combustion of the crystalline Diels-Alder adduct of anthracene and maleic anhydride: C 18 H 12 O 3, was measured with a model 1241 Parr automatic calorimeter and a Parr model 1710 calorimeter controller. The Anthracene-maleic anhydride diels-alder adduct molecule contains a total of 37 bond (s) There are 25 non-H bond (s), 14 multiple bond (s), 2 double bond (s), 12 aromatic bond (s), 1 five-membered ring (s), 5 six-membered ring (s), 2 nine-membered ring (s), 4 ten-membered ring (s), 2 ester (s) (aliphatic) and 1 anhydride (s) (-thio). This experiment involved a reaction between anthracene and maleic anhydride via a Diels Alder reaction to yield 9, 10-dihydroanthracene-9,10-α, β-succinic anhydride. Anthracene was the diene and maleic anhydride was the dienophile. The percent yield of the crude product was 69.03%. The structure data file (SDF/MOL File) contains the information about the atoms, bonds, connectivity and coordinates of Anthracene-maleic anhydride diels-alder adduct molecule. It starts with a header block, followed by "connection table’, which describes the structural relationships and properties of the atoms.

It can be imported to most of the chemistry software for further analysis.