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

Description

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

Uses

Used in Organic Synthesis:
(10-[(Acetyloxy)methyl]-9-anthryl)methyl acetate is used as a reagent in chemical reactions for the synthesis of other organic compounds. Its unique structure and functional groups make it a valuable building block in the preparation of a wide range of organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (10-[(Acetyloxy)methyl]-9-anthryl)methyl acetate is used as a key intermediate in the synthesis of various drug molecules. Its versatility and reactivity in chemical reactions allow for the development of new and innovative pharmaceutical compounds.
Used in Chemical Research:
(10-[(Acetyloxy)methyl]-9-anthryl)methyl acetate is also used in chemical research as a model compound to study various reaction mechanisms and to develop new synthetic methodologies. Its unique properties and reactivity make it an interesting subject for research in the field of organic chemistry.

Upstream product

• 781-43-1 9,10-dimethylanthracene 
• 546-67-8 lead(IV) tetraacetate 
• 64-19-7 acetic acid 
• 10387-13-0 9,1-bis(chloromethyl)anthracene 
• 7072-02-8 9,10-bis-ethoxymethyl-anthracene 
• 120-12-7 anthracene 
• 127-09-3 sodium acetate 
• 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 
• 127-08-2 potassium acetate 

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.