Dibenzosuberane - CAS 833-48-7
Catalog: |
BB037017 |
Product Name: |
Dibenzosuberane |
CAS: |
833-48-7 |
Synonyms: |
tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,11,13-hexaene |
IUPAC Name: | tricyclo[9.4.0.03,8]pentadeca-1(15),3,5,7,11,13-hexaene |
Description: | Dibenzosuberane (CAS# 833-48-7) is used as the base structure of various tricyclic antidepressants. Studies suggest that Dibenzosuberane and its analogues may have anti-viral properties. |
Molecular Weight: | 194.27 |
Molecular Formula: | C15H14 |
Canonical SMILES: | C1CC2=CC=CC=C2CC3=CC=CC=C31 |
InChI: | InChI=1S/C15H14/c1-3-7-14-11-15-8-4-2-6-13(15)10-9-12(14)5-1/h1-8H,9-11H2 |
InChI Key: | PJQCANLCUDUPRF-UHFFFAOYSA-N |
Boiling Point: | 160-165 °C2 mmHg (lit.) |
Melting Point: | 74-76 °C (lit.) |
Purity: | 95 % |
Density: | 1.056 g/cm3 |
Appearance: | Off-white crystals |
LogP: | 3.37600 |
Publication Number | Title | Priority Date |
CN-112175004-A | Method for constructing dibenzosuberone skeleton through free radical cyclization reaction | 20201015 |
CN-112175004-B | Method for constructing dibenzosuberone skeleton through free radical cyclization reaction | 20201015 |
CN-113429559-A | Six-arm polyethylene glycol derivative with end hetero-functionalized and preparation method thereof | 20200323 |
WO-2021154976-A1 | Methods of treating brain cancer with panobinostat | 20200128 |
CN-112321644-A | Spiro dibenzosuberene phosphine oxide compound and application thereof | 20191224 |
PMID | Publication Date | Title | Journal |
23025417 | 20121026 | Dibenzocycloheptanoids from the leaves of Cinnamomum subavenium | Journal of natural products |
22243960 | 20120201 | Structure-based design, synthesis and structure-activity relationships of dibenzosuberyl- and benzoate-substituted tropines as ligands for acetylcholine-binding protein | Bioorganic & medicinal chemistry letters |
22112366 | 20111123 | In vitro antiplasmodial activity of crude extracts of Tetrapleura tetraptera and Copaifera religiosa | BMC research notes |
21413695 | 20110415 | Chiral magnesium BINOL phosphate-catalyzed phosphination of imines: access to enantioenriched α-amino phosphine oxides | Organic letters |
20967908 | 20101115 | Modulation of photoswitching profiles by 10,11-dialkoxymethyl substituents in c(2)-symmetric dibenzosuberane-based helicenes | Chemistry (Weinheim an der Bergstrasse, Germany) |
Complexity: | 186 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 194.109550447 |
Formal Charge: | 0 |
Heavy Atom Count: | 15 |
Hydrogen Bond Acceptor Count: | 0 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 194.109550447 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 0 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 4.5 |
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