10273-84-4

Basic information

• Product Name: (10-[(Acetyloxy)methyl]-9-anthryl)methyl acetate
• Synonyms: (10-[(Acetyloxy)methyl]-9-anthryl)methyl acetate
• CAS NO: 10273-84-4
• Molecular Formula: C20H18 O4
• Molecular Weight: 322.35
• Mol File: 10273-84-4.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (10-[(Acetyloxy)methyl]-9-anthryl)methyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: (10-[(Acetyloxy)methyl]-9-anthryl)methyl acetate(10273-84-4)
• EPA Substance Registry System: (10-[(Acetyloxy)methyl]-9-anthryl)methyl acetate(10273-84-4)

Safety Data

• Hazardous Substances Data: 10273-84-4(Hazardous Substances Data)

Usage

General Description

The chemical "(10-[(Acetyloxy)methyl]-9-anthryl)methyl acetate" is a compound with the molecular formula C26H22O5. It is a derivative of anthracene and contains two acetyl groups. (10-[(Acetyloxy)methyl]-9-anthryl)methyl acetate is primarily used in organic synthesis and as a building block for the preparation of various organic molecules. It is a colorless to pale yellow solid at room temperature and is soluble in organic solvents. Its primary use is as a reagent in chemical reactions for the synthesis of other organic compounds.

Upstream product

• 10387-13-0 9,1-bis(chloromethyl)anthracene 
• 127-08-2 potassium acetate 
• 64-19-7 acetic acid 
• 1187784-90-2 9,10-bis(4-amino-5-phenyl-1,2,4-triazol-3-ylsulfanylmethyl)anthracene 
• 135879-38-8 2,2′-((anthracene-9,10-diylbis(methylene)) bis(oxy))dibenzaldehyde 
• 127-09-3 sodium acetate 
• 120-12-7 anthracene 
• 7072-02-8 9,10-bis-ethoxymethyl-anthracene 
• 781-43-1 9,10-dimethylanthracene 
• 546-67-8 lead(IV) tetraacetate 

Downstream Products

• 7044-91-9 9,10-diformylanthracene 

Relevant articles and documents

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Metal-organic frameworks (MOFs) composed of (triptycenedicarboxylato)zinc

Two novel 2D and 3D coordination polymers of 9,10-trip-tycenedicarboxylic acid and zinc nitrate, which form under solvothermal reaction conditions, are described. As determined by single-crystal X-ray structure analysis, their frameworks are assembled from dinuclear zinc coordination units which are interlinked by triptycenedicarboxylato (TDC) struts. In the 2D-MOF reported here, the extended network of van der Waals interactions between triptycene units as well as coordinated solvent molecules is responsible for the dense assembly of layers with a 44 net topology into the final crystal structure. The framework of the 3D-MOF is composed from [Zn2(TDC) 1.5]∞ layers with a 63 topology, the layers being interlinked by triptycenedicarboxylato pillars (bnn-net). This MOF possesses hexagonal channels which are filled with guest molecules. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

Synthesis of novel amide-crownophanes and Schiff base-crownophanes based on p-phenylene, 2,6-naphthalene, and 9,10-anthracene

(Chemical Equation Presented) The novel macrocyclic diamides 11-13, 16-18 are obtained in 45-66% yields by the reaction of dipotassium salts 10a-c and 15 with each of 1,4-di(bromomethyl)benzene 4, 2,6-di(bromomethyl)naphthalene 6 and 9,10-di(bromomethyl)anthracene 8, repectively, in boiling DMF. On the other hand, the new macrocyclic Schiff bases 28 and 29 are obtained in 44% and 42% yields by heating the appropriate bis-amines 25b, 26b with the corresponding bis-aldehydes 21, 22, respectively, in refluxing acetic acid under high-dilution conditions.