11 -Phenylnaphthalene
- Name 11 -Phenylnaphthalene
- CAS 605-02-7
- Purity 99%
Product Details
Cost-effective and customizable 11 -Phenylnaphthalene 605-02-7 for sale
- Molecular Formula: C16H12
- Molecular Weight: 204.271
- Appearance/Colour: clear colorless to yellow viscous liquid
- Vapor Pressure: 0.000219mmHg at 25°C
- Refractive Index: n20/D 1.664(lit.)
- Boiling Point: 336.4 °C at 760 mmHg
- Flash Point: 148.2 °C
- PSA： 0.00000
- Density: 1.081 g/cm3
- LogP: 4.50680
11 -Phenylnaphthalene(Cas 605-02-7) Usage
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General Description |
11-Phenylnaphthalene is a polycyclic aromatic hydrocarbon chemical compound composed of two fused benzene rings with a phenyl group attached at the 11th carbon. It is a colorless solid at room temperature and is insoluble in water. 11-Phenylnaphthalene is primarily used as a starting material in the production of dyes, pigments, and fluorescent whitening agents. It is also utilized as an intermediate in the synthesis of pharmaceuticals and other organic compounds. However, |
InChI:InChI=1/C16H12/c1-2-7-13(8-3-1)16-12-6-10-14-9-4-5-11-15(14)16/h1-12H
605-02-7 Relevant articles
Palladium-catalyzed coupling of aryl halides with arylhalosilanes in air and water
Huang, Taisheng,Li, Chao-Jun
, p. 403 - 405 (2002)
In the presence of a palladium catalyst,...
A highly acid labile silicon linker for solid phase synthesis
Hone, Neal D.,Davies, Stephen G.,Devereux, Nicholas J.,Taylor, Sara L.,Baxter, Anthony D.
, p. 897 - 900 (1998)
A novel arylsilane based linker has been...
One-pot Solvent-free Catalytic Dimerization Reaction of Phenylacetylene to 1-Phenylnaphthalene
Taherpour, Avat,Taban, Sepehr,Yari, Ako
, p. 1523 - 1530 (2015)
In this study, we report a smooth one-po...
Confinement effects at the external surface of delaminated zeolites (ITQ-2): An inorganic mimic of cyclodextrins
Galletero, Mariì?a S.,Corma, Avelino,Ferrer, Beleì?n,Forneì?s, Vicente,Garciì?a, Hermenegildo
, p. 1135 - 1141 (2003)
Novel delaminated ITQ-2 zeolite has a re...
Solid-supported palladium nano and microparticles: An efficient heterogeneous catalyst for ligand-free Suzuki-Miyaura cross coupling reaction
Das, Pralay,Sharma, Dharminder,Shil, Arun K.,Kumari, Avnesh
, p. 1176 - 1178 (2011)
Solid-supported nano and microparticles ...
Pd(II)-catalyzed synthesis of unsymmetrical biaryls from tetraphenylborate and aryl halides under microwave activation
Wang, Jin-Xian,Yang, Yihua,Wei, Bangguo
, p. 2063 - 2069 (2004)
A rapid and efficient method for synthes...
Deposited zirconocene chloride on silica-layered CuFe2O4 as a highly efficient and reusable magnetically nanocatalyst for one-pot Suzuki-Miyaura coupling reaction
Zeynizadeh, Behzad,Sepehraddin, Farhad
, p. 70 - 77 (2018)
The novel core-shell magnetically nanopa...
Heterogeneous Suzuki reactions catalyzed by Pd(0)-Y zeolite
Artok, Levent,Bulut, Hatice
, p. 3881 - 3884 (2004)
The Pd(0)-Y zeolite showed high activity...
Combination of polymer and halloysite chemistry for development of a novel catalytic hybrid system
Sadjadi, Samahe,Malmir, Masoumeh,Pourmohammad, Nargess,Ahmadi, Shervin,Heravi, Majid M.
, p. 4349 - 4366 (2019)
Abstract: A covalent hybrid of halloysit...
Highly dispersed palladium(II) in a defective metal-organic framework: Application to C-H activation and functionalization
Park, Tae-Hong,Hickman, Amanda J.,Koh, Kyoungmoo,Martin, Stephen,Wong-Foy, Antek G.,Sanford, Melanie S.,Matzger, Adam J.
, p. 20138 - 20141 (2011)
High reversibility during crystallizatio...
Stereo- and Regio-specific Photochemical Cycloaddition of Furan to Benzonitrile and Phenylacetylene
Gilbert, Andrew,Rodwell, Paul
, p. 1057 - 1058 (1985)
Benzonitrile and phenylacetylene undergo...
A green and efficient Pd-free protocol for the Suzuki–Miyaura cross-coupling reaction using Fe3O4@APTMS@Cp2ZrClx(x = 0, 1, 2) MNPs in PEG-400
Zeynizadeh, Behzad,Mousavi, Hossein,Sepehraddin, Farhad
, p. 3361 - 3382 (2020)
Abstract: In this paper, a new applicati...
Silver(I), mercury(II) and palladium(II) complexes of functionalized N-heterocyclic carbenes: Synthesis, structural studies and catalytic activity
Liu, Qing-Xiang,Li, Hui-Long,Zhao, Xiao-Jun,Ge, Shu-Sheng,Shi, Meng-Chao,Shen, Gang,Zang, Yan,Wang, Xiu-Guang
, p. 437 - 445 (2011)
A series of NHC silver(I), mercury(II) a...
Selective and efficient synthesis of decahedral palladium nanoparticles and its catalytic performance for Suzuki coupling reaction
Patil, Aniruddha B.,Patil, Dinkar S.,Bhanage, Bhalchandra M.
, p. 146 - 153 (2012)
A convenient, mild and cost-effective sy...
Electrostatic Grafting of a Palladium N-Heterocyclic Carbene Catalyst on a Periodic Mesoporous Organosilica and its Application in the Suzuki-Miyaura Reaction
Rajabi, Fatemeh,Schaffner, Dirk,Follmann, Sascha,Wilhelm, Christian,Ernst, Stefan,Thiel, Werner R.
, p. 3513 - 3518 (2015)
A periodic mesoporous organosilica mater...
Synthesis and characterization of palladium nanoparticles immobilized on graphene oxide functionalized with triethylenetetramine or 2,6-diaminopyridine and application for the Suzuki cross-coupling reaction
Mirza-Aghayan, Maryam,Mohammadi, Marzieh,Boukherroub, Rabah
, (2021/11/22)
Graphene oxide (GO) was functionalized w...
Pd–Ni bimetallic catalyst supported on dendrimer-functionalized magnetic graphene oxide for efficient catalytic Suzuki-Miyaura coupling reaction
Masteri-Farahani, Majid,Niakan, Mahsa
, (2022/01/26)
A novel type of dendritic structure was ...
Ring Contraction of Tropylium Ions into Benzenoid Derivatives
Crocker, Reece D.,Dinh, An H.,Lyons, Demelza J. M.,Mai, Binh Khanh,Nguyen, Thanh Vinh,Ton, Nhan N. H.
supporting information, p. 2520 - 2525 (2022/04/12)
We report a method to convert substitute...
Fe3O4-SAHPG-Pd0 nanoparticles: A ligand-free and low Pd loading quasiheterogeneous catalyst active for mild Suzuki–Miyaura coupling and C-H activation of pyrimidine cores
Azizollahi, Hamid,Eshghi, Hossein,García-López, José-Antonio
, (2020/09/17)
This paper reports a green magnetic quas...
605-02-7 Process route
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98-81-7
1-bromovinylbenzene
-
-
100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6
styrene
-
-
1445-78-9
2,5-Diphenyl-thiophene
-
-
605-02-7
1-phenylnaphthalene
-
-
α-styryl-β-styryl sulfide
| Conditions | Yield |
|---|---|
|
With
hydrogen sulfide;
at 170 ℃;
for 4h;
|
20%
12.8% 8.5% 37% |
-
-
98-81-7
1-bromovinylbenzene
-
-
100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6
styrene
-
-
605-02-7
1-phenylnaphthalene
| Conditions | Yield |
|---|---|
|
at 170 ℃;
for 10h;
|
2.4%
75% |
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