1468-95-7
- Product Name：9-Anthracenemethanol
- Molecular Formula：C15H12O
- Purity：99%
- Molecular Weight：208.26
Product Details
pd_meltingpoint:160-164 ºC
Appearance:light yellow solid
Purity:99%
Reputable supplier selling 9-Anthracenemethanol 1468-95-7 with stock
- Molecular Formula:C15H12O
- Molecular Weight:208.26
- Appearance/Colour:light yellow solid
- Vapor Pressure:6.35E-08mmHg at 25°C
- Melting Point:160-164 ºC
- Refractive Index:1.729
- Boiling Point:423.4ºC at 760 mmHg
- PKA:14.36±0.10(Predicted)
- Flash Point:196.3 ºC
- PSA：20.23000
- Density:1.214 g/cm3
- LogP:3.48530
9-Anthracenemethanol(Cas 1468-95-7) Usage
|
Preparation |
9-Anthracenemethanol is synthesized by hydrogenation of 9-anthracenecarboxaldehyde. It is a versatile precursor to supramolecular assemblies. |
|
Safety Profile |
Mutation data reported. Whenheated to decomposition it emits acrid smoke andirritating vapors. |
|
General Description |
9-Anthracenemethanol participates in ring-opening polymerization of L-lactide catalyzed by alumoxane. It undergoes proton exchange reaction with potassium tert-butoxide to yield potassium 9-anthracenemethoxide. |
InChI:InChI=1/C15H12O/c16-10-15-13-7-3-1-5-11(13)9-12-6-2-4-8-14(12)15/h1-9,16H,10H2
1468-95-7 Relevant articles
Light- and heat-triggered reversible luminescent materials based on polysiloxanes with anthracene groups
Han, Dongdong,Lu, Hang,Li, Wensi,Li, Yonghao,Feng, Shengyu
, p. 56489 - 56495 (2017)
In this study, reversible silicone elast...
A Fluorescent Silver(I) Carbene Complex with Anticancer Properties: Synthesis, Characterization, and Biological Studies
Fabbrini, Maria Giulia,Cirri, Damiano,Pratesi, Alessandro,Ciofi, Lorenzo,Marzo, Tiziano,Guerri, Annalisa,Nistri, Silvia,Dell'Accio, Alfonso,Gamberi, Tania,Severi, Mirko,Bencini, Andrea,Messori, Luigi
, p. 182 - 188 (2019)
The silver(I) N-heterocyclic carbene (NH...
A simple and robust PET-based anthracene-appended O-N-O chelate for sequential recognition of Fe3+/CN– ions in aqueous media and its multimodal applications
Pandith, Anup,Choi, Jun-Hyeak,Jung, Ok-Sang,Kim, Hong-Seok
, p. 669 - 680 (2018)
A very simple, robust, and pico/nanomola...
Synthesis of 9-Substituted Triptycene Building Blocks for Solid-Phase Diversification and Nucleic Acid Junction Targeting
Yoon, Ina,Suh, Sung-Eun,Barros, Stephanie A.,Chenoweth, David M.
, p. 1096 - 1099 (2016)
Triptycenes have been shown to bind nucl...
Activation of promutagens by endogenous and heterologous sulfotransferases expressed in continuous cell cultures
Glatt, Hansruedi,Pauly, Karin,Piee-Staffa, Andrea,Seidel, Albrecht,Hornhardt, Sabine,Czich, Andreas
, p. 13 - 22 (1994)
various environmental chemical are metab...
Preparation and characterisation of fluorescent chitosans using 9-anthraldehyde as fluorophore
Tommeraas, Kristoffer,Strand, Sabina P.,Tian, Wei,Kenne, Lennart,Varum, Kjell M.
, p. 291 - 296 (2001)
Chitosans with chemical composition rang...
Experimental and DFT studies on the vibrational and electronic spectra of 9-anthracenemethanol
Kou, Shanshan,Zhou, Hu,Tang, Guodong,Li, Rongqing,Zhang, Yu,Zhao, Jianying,Wei, Changmei
, p. 768 - 775 (2012)
Vibrational spectral measurements were m...
-
Schreiber,K.C.,Emerson,W.
, p. 95 - 99 (1966)
-
A Photo-Triggered Traceless Staudinger–Bertozzi Ligation Reaction
Hu, Peng,Feng, Tianshi,Yeung, Chi-Chung,Koo, Chi-Kin,Lau, Kai-Chung,Lam, Michael H. W.
, p. 11537 - 11542 (2016)
The use of light to control the course o...
Fluorometric analysis of borohydrides based on reductive aldehyde-to-alcohol conversion of arylaldehydes
Kim, Na Yeong,Baek, Ji Hye,Chang, Suk-Kyu
, p. 59 - 62 (2019)
Fluorometric analysis of borohydride (BH...
The synthesis of a new type of anthracene DNA intercalator
Ostaszewski, Ryszard,Wilczynska, Edyta,Wolszczak, Marian
, p. 2995 - 2996 (1998)
A new type of DNA intercalator based on ...
An easy synthesis of lepidopterene from 9-chloromethyl anthracene. Evidence for a free radical mechanism
Fernández, María-José,Gude, Lourdes,Lorente, Antonio
, p. 891 - 893 (2001)
This communication reports a novel and e...
Aromatic thioesters as protecting groups for thiols against 1,2-didehydrobenzenes
Fowelin, Christian,Schuepbach, Bjoern,Terfort, Andreas
, p. 1013 - 1017 (2007)
Divalent sulfur compounds usually react ...
Synthesis of a New Fluorescent Probe Specific for Catechols
Stack, Douglas E.,Hill, Anastacia L.,Diffendaffer, Clark B.,Burns, Nicole M.
, p. 4487 - 4490 (2002)
(Matrix Presented) The synthesis of a ne...
Synthesis of corrole-fullerene dyads via [4 + 2] cycloaddition reaction
Li, Chengjie,Zhang, Jie,Liu, Xiujun,Zhou, Yongzhu,Sun, Dongming,Cheng, Ping,Zhang, Bao,Feng, Yaqing
, p. 40758 - 40762 (2014)
Three corrole-fullerene dyads were prepa...
[60]Fullerene adducts with 9-substituted anthracenes: Mechanochemical preparation and retro Diels-Alder reaction
Wang, Guan-Wu,Chen, Zhong-Xiu,Murata, Yasujiro,Komatsu, Koichi
, p. 4851 - 4856 (2005)
Three 9-substituted anthracene derivativ...
Arene-ruthenium complexes with 2-(arylazo)phenol as ancillary ligand: Synthesis, characterization, and utilization in catalytic transfer-hydrogenation
Karmakar, Jit,Bhattacharya, Samaresh
, p. 39 - 44 (2019)
Reaction of 2-(arylazo)phenols (HL-R, wh...
Chemical syntheses of novel fluorescent labelled fatty acids, phosphatidylcholines and cholesterol esters
Stoffel,Michaelis
, p. 7 - 19 (1976)
The synthesis of a novel class of fluore...
-
Greene et al.
, p. 3852,3855 (1955)
-
Expected and unexpected photoreactions of 9-(10-)substituted anthracene derivatives in cucurbit[: N] uril hosts
Hu, Xianchen,Liu, Fengbo,Liu, Simin,Zhang, Xiongzhi,Zhao, Zhiyong
, p. 4779 - 4785 (2020)
By arranging substrates in a reaction r...
Porphyrin-Cored Polymer Nanoparticles: Macromolecular Models for Heme Iron Coordination
Rodriguez, Kyle J.,Hanlon, Ashley M.,Lyon, Christopher K.,Cole, Justin P.,Tuten, Bryan T.,Tooley, Christian A.,Berda, Erik B.,Pazicni, Samuel
, p. 9493 - 9496 (2016)
Porphyrin-cored polymer nanoparticles (P...
Dual utility of a single diphosphine-ruthenium complex: A precursor for new complexes and, a pre-catalyst for transfer-hydrogenation and Oppenauer oxidation
Mukherjee, Aparajita,Bhattacharya, Samaresh
, p. 15617 - 15631 (2021/05/19)
The diphosphine-ruthenium complex, [Ru(d...
PHOTOLYTIC COMPOUNDS AND TRIPLET-TRIPLET ANNIHILATION MEDIATED PHOTOLYSIS
-
Paragraph 0026, (2021/04/17)
The invention provides novel photolytic ...
Small-Molecule Investigation of Diels-Alder Complexes for Thermoreversible Crosslinking in Polymeric Applications
Rowlett, Jarrett R.,Deglmann, Peter,Sprafke, Johannes,Roy, Nabarun,Mülhaupt, Rolf,Bruchmann, Bernd
, p. 8933 - 8944 (2021/07/20)
Combinations of dienes and dienophiles w...
BiCl3-Facilitated removal of methoxymethyl-ether/ester derivatives and DFT study of -O-C-O- bond cleavage
Pacherille, Angela,Tuga, Beza,Hallooman, Dhanashree,Dos Reis, Isaac,Vermette, Mélodie,Issack, Bilkiss B.,Rhyman, Lydia,Ramasami, Ponnadurai,Sunasee, Rajesh
supporting information, p. 7109 - 7116 (2021/05/03)
A simple method for the cleavage of meth...
1468-95-7 Process route
-
-
4671-58-3
N-Benzoyl-glycin-<9>-anthrylmethylester
-
-
495-69-2,140480-84-8,21251-67-2,91787-63-2,66407-11-2
Hippuric Acid
-
-
1468-95-7
9-hydroxymethylanthracene
| Conditions | Yield |
|---|---|
|
In
water; acetonitrile;
for 0.166667h;
Quantum yield;
Photolysis;
|
51 % Chromat. |
-
-
23674-17-1
9-bromo-10-methylanthracene
-
-
1468-95-7
9-hydroxymethylanthracene
-
-
779-02-2
9-methylanthracene
-
-
84-65-1
9,10-phenanthrenequinone
-
-
86170-51-6
(trimethyl-2,4,6 phenoxy)methyl-9 anthracene
| Conditions | Yield |
|---|---|
|
With
trimethyl-2,4,6 phenate de potassium;
In
N,N,N,N,N,N-hexamethylphosphoric triamide;
at 100 ℃;
for 10h;
|
18% 6.5% 8.5% 31.5% |
1468-95-7 Upstream products
-
67-63-0
isopropyl alcohol
-
642-31-9
9-anthracene aldehyde
-
67-56-1
methanol
-
2417-77-8
9-bromoethylanthracene
1468-95-7 Downstream products
-
24463-19-2
anthracenylmethyl chloride
-
529-85-1
9-fluoroantracene
-
642-31-9
9-anthracene aldehyde
-
80615-69-6
(9-anthranylmethyloxymethyl)-benzene
Relevant Products
-
Tris(2-(2-methoxyethoxy)ethyl)amineCAS：70384-51-9
-
1-Bromo-3-chloropropaneCAS：109-70-6
-
2-Bromobutyric acidCAS：80-58-0
