9-methylidenefluorene

Catalog Number Size Price Stock Quantity
B0001-285837 500 mg $439 In stock
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Product Information

Molecular Formula:
C14H10
Molecular Weight:
178.23
Description
9-Methylidenefluorene is an analog of 9-Methylfluorene; a compound that has been shown to be mutagenic in Salmonella typhimurium TA98 and TA100 in the presence of 9000 X g supernantant from Aroclor-induced rats.
Synonyms
9-Methylene-9H-fluorene; 9H-Fluorene, 9-Methylene-; Fluorenylidenemethane; 9-Methylene-fluorene
IUPAC Name
9-methylidenefluorene
Canonical SMILES
C=C1C2=CC=CC=C2C3=CC=CC=C13
InChI
InChI=1S/C14H10/c1-10-11-6-2-4-8-13(11)14-9-5-3-7-12(10)14/h2-9H,1H2
InChI Key
ZYASLTYCYTYKFC-UHFFFAOYSA-N
Boiling Point
305.9±12.0 °C (Predicted)
Melting Point
46-48 °C
Density
1.12±0.1 g/cm3(Predicted)
Appearance
Solid
Storage
Amber Vial, -20 °C Freezer, Under inert atmosphere

Safety Information

Hazards
H302:
Harmful if swallowed.
H401:
Toxic to aquatic life.
H411:
Toxic to aquatic life with long-lasting effects.
Precautionary Statement
P273:
Avoid release to the environment.
P301:
IF SWALLOWED:
P312:
Call a POISON CENTER or doctor/physician if you feel unwell.

Computed Properties

XLogP3
3.7
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
0
Exact Mass
178.078250319 g/mol
Monoisotopic Mass
178.078250319 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
14
Formal Charge
0
Complexity
216
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-113354514-A Method for controllable high-selectivity synthesis of 9-fluorenylmethanol and 9, 9-bis (hydroxymethyl) fluorene 2021-06-07
CN-112608222-A Method for preparing aldehyde ketone compound by olefin oxidation 2020-12-03
CN-111362955-A Organic compound and application thereof to OLED device 2018-12-26
US-2020016185-A1 Senolytic compositions and uses thereof 2018-07-11
WO-2020014409-A1 Senolytic compositions and uses thereof 2018-07-11
CA-3105982-A1 Senolytic compositions and uses thereof 2018-07-11
CN-112469697-A Anti-aging composition and application thereof 2018-07-11
EP-3790861-A1 Senolytic compositions and uses thereof 2018-07-11
KR-20210030905-A Senolytic composition and use thereof 2018-07-11
US-11026963-B2 Senolytic compositions and uses thereof 2018-07-11

Literatures

PMID Publication Date Title Journal
22327299 2012-03-21 Design of small molecule reagents that enable signal amplification via an autocatalytic, base-mediated cascade elimination reaction Chemical communications (Cambridge, England)
21210693 2011-02-03 Controlling the spatial orientation of molecular actuators: polarized photoisomerization of 2-nitro-9-(2,2,2-triphenylethylidene)fluorene in a thin polymer matrix The journal of physical chemistry. A
20725626 2010-06-13 Synthesis and g-quadruplex-binding properties of defined acridine oligomers Journal of nucleic acids
21140921 2010-01-01 Thermal cleavage of the fmoc protection group Chimia
21197436 2010-01-01 Synthesis of Peptides from α- and β-Tubulin Containing Glutamic Acid Side-Chain Linked Oligo-Glu with Defined Length International journal of peptides
16366613 2005-12-29 Syntheses, structures, and photoisomerization of (E)- and (Z)-2-tert-butyl-9-(2,2,2-triphenylethylidene)fluorene The journal of physical chemistry. A
18969837 2005-01-30 Measurement of the FMOC loading of protected amine-functionalised polymer beads Talanta
11552835 2001-09-19 Dibenzofulvene, a 1,1-diphenylethylene analogue, gives a pi-stacked polymer by anionic, free-radical, and cationic catalysts Journal of the American Chemical Society
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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