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About This Item
Empirical Formula (Hill Notation):
C14H6F2O2
CAS Number:
Molecular Weight:
244.19
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
Quality Level
Assay
96%
mp
228-232 °C (lit.)
SMILES string
Fc1ccc(F)c2C(=O)c3ccccc3C(=O)c12
InChI
1S/C14H6F2O2/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-6H
InChI key
DTNCXQHDOJRTCD-UHFFFAOYSA-N
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Heterogeneous organocatalysis for the asymmetric desymmetrization of meso-cyclic anhydrides using silica gel-supported bis-cinchona alkaloids.
Kim HS, et al.
Tetrahedron, 60(52), 12051-12051 (2004)
Synthesis of a New Chiral Ligand (QN)2AQN and Its Application to the Catalytic Asymmetric Aminohydroxylation of Methyl Cinnamates.
Si-Kun C, et al.
Chin. J. Chem., 25(8), 982-986 (2005)
Synthesis of fluorine-substituted anthraquinones and aza-anthraquinones.
Khanapure SP, et al.
Journal of Fluorine Chemistry, 68(2), 131-134 (1994)
H-J Lehmler et al.
Tetrahedron, 66(14), 2561-2569 (2010-03-23)
A series of colored hydrocarbon and fluorocarbon tagged 1-fluoro-4-alkylamino-anthraquinones and 1,4-bis-alkylamino-anthraquinone probe molecules were synthesized from a (fluorinated) alkyl amine and 1,4-difluoroanthraquinone to aid in the development of fluorous separation applications. The anthraquinones displayed stacking of the anthraquinone tricycle and
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