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MedKoo Cat#: 581679 | Name: Decacyclene

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Decacyclene is a biochemical.

Chemical Structure

Decacyclene
Decacyclene
CAS#191-48-0

Theoretical Analysis

MedKoo Cat#: 581679

Name: Decacyclene

CAS#: 191-48-0

Chemical Formula: C36H18

Exact Mass: 450.1409

Molecular Weight: 450.54

Elemental Analysis: C, 95.97; H, 4.03

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
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Synonym
Decacyclene; EINECS 205-889-0; Diacenaphtheno(1,2-j:1',2'-l)fluoranthen; NSC 60676; UNII-EZG7J41ZUH.
IUPAC/Chemical Name
diacenaphtho[1,2-j:1',2'-l]fluoranthene
InChi Key
CUIWZLHUNCCYBL-UHFFFAOYSA-N
InChi Code
InChI=1S/C36H18/c1-7-19-8-2-14-23-28(19)22(13-1)31-32(23)34-26-17-5-11-21-12-6-18-27(30(21)26)36(34)35-25-16-4-10-20-9-3-15-24(29(20)25)33(31)35/h1-18H
SMILES Code
c12c(c3c4c1cccc4ccc3)c1c(c3c4c5c(cccc5ccc4)c23)c2c3c1cccc3ccc2
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 450.54 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Yamamoto Y, Yoshida M, Morii T, Nishida JI, Kitamura C, Kawase T. Synthesis and Properties of a Decacyclene Monoimide and a Naphthalimide Derivative as Three-Dimensional Acceptor-Donor-Acceptor Systems. Chem Asian J. 2018 Apr 4;13(7):790-798. doi: 10.1002/asia.201701668. Epub 2018 Mar 2. PubMed PMID: 29405632. 2: Sumy DP, Dodge NJ, Harrison CM, Finke AD, Whalley AC. Tridecacyclene: A Cyclic Tetramer of Acenaphthylene. Chemistry. 2016 Mar 24;22(14):4709-12. doi: 10.1002/chem.201600165. Epub 2016 Feb 17. PubMed PMID: 26791961. 3: de Oteyza DG, Garcia-Lastra JM, Toma FM, Borghetti P, Floreano L, Verdini A, Cossaro A, Pho TV, Wudl F, Ortega JE. Decacyclene Trianhydride at Functional Interfaces: An Ideal Electron Acceptor Material for Organic Electronics. J Phys Chem Lett. 2016 Jan 7;7(1):90-5. doi: 10.1021/acs.jpclett.5b02562. Epub 2015 Dec 17. PubMed PMID: 26651535. 4: Toma FM, Puntoriero F, Pho TV, La Rosa M, Jun YS, Tremolet de Villers BJ, Pavlovich J, Stucky GD, Campagna S, Wudl F. Polyimide dendrimers containing multiple electron donor-acceptor units and their unique photophysical properties. Angew Chem Int Ed Engl. 2015 Jun 1;54(23):6775-9. doi: 10.1002/anie.201501298. Epub 2015 Apr 27. PubMed PMID: 25925409. 5: Cataldo F, Angelini G, García-Hernández DA, Manchado A. Far infrared (terahertz) spectroscopy of a series of polycyclic aromatic hydrocarbons and application to structure interpretation of asphaltenes and related compounds. Spectrochim Acta A Mol Biomol Spectrosc. 2013 Jul;111:68-79. doi: 10.1016/j.saa.2013.03.077. Epub 2013 Mar 26. PubMed PMID: 23603577. 6: Pawin G, Stieg AZ, Skibo C, Grisolia M, Schilittler RR, Langlais V, Tateyama Y, Joachim C, Gimzewski JK. Amplification of conformational effects via tert-butyl groups: hexa-tert-butyl decacyclene on Cu(100) at room temperature. Langmuir. 2013 Jun 18;29(24):7309-17. doi: 10.1021/la304634n. Epub 2013 Jan 30. PubMed PMID: 23311621. 7: Pho TV, Toma FM, Chabinyc ML, Wudl F. Self-assembling decacyclene triimides prepared through a regioselective hextuple Friedel-Crafts carbamylation. Angew Chem Int Ed Engl. 2013 Jan 28;52(5):1446-51. doi: 10.1002/anie.201207608. Epub 2012 Dec 17. PubMed PMID: 23255510. 8: Wesoloski LM, Stieg AZ, Kunitake M, Dultz SC, Gimzewski JK. Observations of image contrast and dimerization of decacyclene by low temperature scanning tunneling microscopy. J Chem Phys. 2007 Nov 7;127(17):174703. PubMed PMID: 17994838. 9: Schneider JJ, Spickermann D, Lehmann CW, Magull J, Krüger HJ, Ensling J, Gütlich P. Decacyclene as complexation manifold: synthesis, structure and properties of its Fe2 and Fe4 slipped triple-decker complexes. Chemistry. 2006 Feb 1;12(5):1427-35. PubMed PMID: 16276505. 10: Fialkov AB, Gordin A, Amirav A. Extending the range of compounds amenable for gas chromatography-mass spectrometric analysis. J Chromatogr A. 2003 Apr 4;991(2):217-40. PubMed PMID: 12741601. 11: Schunack M, Laegsgaard E, Stensgaard I, Johannsen I, Besenbacher F. A Chiral Metal Surface. Angew Chem Int Ed Engl. 2001 Jul 16;40(14):2623-2626. doi: 10.1002/1521-3773(20010716)40:14<2623::AID-ANIE2623>3.0.CO;2-X. PubMed PMID: 29712303. 12: Amirav A, Gordin A, Tzanani N. Supersonic gas chromatography/mass spectrometry. Rapid Commun Mass Spectrom. 2001;15(10):811-20. PubMed PMID: 11344542. 13: Schneider JJ, Spickermann D, Labahn T, Magull J, Fontani M, Laschi F, Zanello P. Mono-, di-, and trimetallic complexes of the nonalternating polycondensed pi-perimeter decacyclene, C36H18: synthesis, structure, and spectroelectrochemistry of. Chemistry. 2000 Oct 16;6(20):3686-91. PubMed PMID: 11073238.