71339-55-4

Basic information

• Product Name: 9-hydroxymethyl-10-methylanthracene
• Synonyms: 9-hydroxymethyl-10-methylanthracene
• CAS NO: 71339-55-4
• Molecular Formula: C₁₆H₁₄O
• Molecular Weight: 0
• Mol File: 71339-55-4.mol

Chemical Properties

• Boiling Point: 435.5°C at 760 mmHg
• Flash Point: 196.3°C
• Appearance: /
• Density: 1.183g/cm³
• Vapor Pressure: 2.35E-08mmHg at 25°C
• Refractive Index: 1.708
• CAS DataBase Reference: 9-hydroxymethyl-10-methylanthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 9-hydroxymethyl-10-methylanthracene(71339-55-4)
• EPA Substance Registry System: 9-hydroxymethyl-10-methylanthracene(71339-55-4)

Safety Data

• Hazardous Substances Data: 71339-55-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H14O/c1-11-12-6-2-4-8-14(12)16(10-17)15-9-5-3-7-13(11)15/h2-9,17H,10H2,1H3

Upstream product

• 56460-15-2 cis-9,10-dihydro-anthracene-9,10-dicarboxylic acid dimethyl ester 
• 875442-12-9 trans-9,10-dihydro-anthracene-9,10-dicarboxylic acid dimethyl ester 
• 123-51-3 i-Amyl alcohol 
• 3114-06-5 cis-9,10-bis(hydroxymethyl)-9,10-dihydroanthracene 
• 917-54-4 methyllithium 
• 84-65-1 9,10-phenanthrenequinone 
• 7072-00-6 10-methyl-9-anthraldehyde 
• 781-43-1 9,10-dimethylanthracene 
• 3114-05-4 trans-9,10-bis-hydroxymethyl-9,10-dihydro-anthracene 
• 17104-29-9 9r.10t-dimethyl-9.10-dihydro-anthracenediol-(9.10c) 

Downstream Products

• 309928-74-3 3-bromo-benzoic acid 10-methyl-anthracen-9-ylmethyl ester 
• 34373-96-1 9,10-dibromomethylanthracene 
• 309929-00-8 4-bromo-benzoic acid 10-methyl-anthracen-9-ylmethyl ester 
• 34331-95-8 9-bromomethyl-10-methylanthracene 

Relevant articles and documents

Energy Migration and Formation in Quasi-Two-Dimensional Polymer Films As Revealed by the Time-Resolved Fluorescence Depolarization Measurement

Excitation energy migration and subsequent energy transfer to excimer-forming sites occurring in a quasi-two-dimensional plane of poly(isobutyl methacrylate) Langmuir-Blodgett films were investigated through the time-resolved analyses of anthracene fluorescence. Fluorescence anisotropy decays showed that the energy migration occurred more efficiently as the anthracene fraction increased. A further increase of the anthracene gave rise to the excimer-forming sites acting as energy traps, and finally the anthracene fluorescence was markedly quenched from the energy transfer to the traps. The migration process was quantitatively analyzed by a computer simulation based on the Monte Carlo method, which allowed estimation of the number of hopping and the mean-square displacement of excitons. The initial growth of the mean-square displacement with time became gradually gentle, while the number of hopping linearly increased with time. This result shows that the excitons are not diffusive and tend to stay within a small cluster of chromophores, especially for small chromophore density at short times.

Synthesis and transformations of a few 9-(pent-4-yn-1-yl)anthracene-type systems

9-(Pent-4-yn-1-yl)anthracene-type compounds can potentially undergo intramolecular Diels-Alder (IMDA) reaction to form 9,11-annulated dibenzobarrelenes. Herein we report the synthesis and IMDA reactions of several heteroatom incorporated 9-(pent-4-yn-1-yl)anthracene-type compounds.