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Benzene, 1-methyl-3-(phenylethynyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14635-91-7

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14635-91-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14635-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,3 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14635-91:
(7*1)+(6*4)+(5*6)+(4*3)+(3*5)+(2*9)+(1*1)=107
107 % 10 = 7
So 14635-91-7 is a valid CAS Registry Number.

14635-91-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3-(2-phenylethynyl)benzene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14635-91-7 SDS

14635-91-7Relevant academic research and scientific papers

Copper-free Sonogashira cross-coupling reactions catalyzed by an efficient dimeric C,N-palladacycle in DMF/H2O

Karami, Kazem,Haghighat Naeini, Nasrin

, p. 1199 - 1207 (2015)

Very small concentrations of a dimeric C,N-palladacycle were used as an efficient homogeneous catalyst for Sonogashira cross-coupling reactions between various aryl halides and phenylacetylene. The catalytic reactions were performed without the need for copper in DMF/H2O. This catalytic system shows excellent yields for aryl iodides and bromides and even in the case of aryl chlorides.

Decorated palladium nanoparticles on mesoporous organosilicate as an efficient catalyst for Sonogashira coupling reaction

Mohajer, Fatemeh,Mohammadi Ziarani, Ghodsi,Badiei, Alireza

, p. 589 - 601 (2021)

Abstract: Reforming mesoporous silica was provided by the reaction of SBA‐15 with (3-aminopropyl)triethoxysilane, the product of which was treated with furfural to give SBA-propyl-imine-furan. In the next step, palladium chloride was attached to the funct

Phosphine-free copper-mediated Sonogashira coupling reaction

Borude, Vasant S.,Shah, Rikhil V.,Shukla, Sanjeev R.

, p. 1663 - 1669 (2013)

A new, efficient, and inexpensive system has been developed to catalyze Sonogashira cross-coupling reactions between aryl iodides and terminal alkynes. We have employed CuO as well as a novel polymer-supported Cu-N-heterocyclic carbene complex, synthesize

Alternating magnetic field mediated micro reaction system for palladium-catalyzed coupling reactions

Kim, Hee Jae,Choi, Jinseop,Choe, Jaehoon,Song, Kwang Ho,Lee, Sunwoo

, p. 37181 - 37184 (2017)

A continuous flow reaction system in which a palladium magnetic catalyst was immobilized and vibrated by an alternating induced magnetic field was developed. The alternating electromagnetic field improved the mixing efficiency and catalytic activity for the palladium-catalyzed coupling reactions. This flow reaction system showed good product yields for various reactions such as Sonogashira, Heck, Suzuki, Stille, Hiyama and decarboxylative coupling reactions.

Heterogeneous copper-free Sonogashira coupling reaction catalyzed by a reusable palladium Schiff base complex in water

He, Ying,Cai, Chun

, p. 2689 - 2692 (2011)

Heterogeneous Sonogashira coupling of terminal alkynes with aryl halides was studied over a polymer-supported macrocyclic Schiff base palladium complex. The cross-coupling reaction proceeded smoothly by adding a piperidine in water medium. The catalyst ex

A 1D palladium coordination polymer and its catalytic activity in microwave-assisted Sonogashira reactions

Lee, Gang Min,Lee, Soon W.

, (2021)

A palladium coordination polymer, [Pd(dppp)(L)](OTf)2·(H2O)] (1) (dppp = 1,3-bis(diphenylphosphino)propane), was prepared from a bipyridine-type ligand (L = (4-py)–CH = N–C10H6–N = CH–(4-py)) and [Pd(dppp)](OTf)

Reduced graphene oxide supported Cu2O nanoparticles as an efficient catalyst for Sonogashira coupling reaction

Wang, Bing,Wang, Yingyong,Guo, Xiaoning,Jiao, Zhifeng,Jin, Guoqiang,Guo, Xiangyun

, p. 36 - 39 (2017)

Reduced graphene oxide supported Cu2O nanoparticles were prepared by a liquid-phase reduction method and employed as an efficient heterogeneous catalyst for Sonogashira cross-coupling reaction. The catalyst exhibits high activity and selectivit

Synthesis of octasubstituted cyclooctatetraenes and their use as electron transporters in organic light emitting diodes

Lu, Ping,Hong, Haiping,Cai, Guoping,Djurovich, Peter,Weber, William P.,Thompson, Mark E.

, p. 7480 - 7486 (2000)

The synthesis and characterization of octasubstituted cyclooctatetraenes (COTs) as well as their use as electron transporting materials in organic LEDs are reported. Tetraaryl-tetraarylethynyl-cyclooctatetraenes [C8Ar4(C≡CAr)4/

Photocatalytic Sonogashira reaction over silicon carbide supported Pd-Cu alloy nanoparticles under visible light irradiation

Wang, Bing,Wang, Yingyong,Li, Jiazhou,Guo, Xiaoning,Bai, Gailing,Tong, Xili,Jin, Guoqiang,Guo, Xiangyun

, p. 3357 - 3362 (2018)

The Sonogashira reaction is an important reaction for forming carbon-carbon bonds in organic synthesis, which is typically carried out under harsh reaction conditions. We herein report that PdCu alloy nanoparticles supported on SiC can efficiently catalyz

Functionalized graphene oxide anchored to Ni complex as an effective recyclable heterogeneous catalyst for Sonogashira coupling reactions

Naeimi, Hossein,Kiani, Fatemeh

, p. 65 - 72 (2019)

The Sonogashira cross coupling reaction is an applied method for preparation of diarylethyne compounds from readily available aryl halide derivatives and phenyl acetylene. The coupling reaction using nickel complex of N,N′-Bis(2-hydroxyethyl)ethylenediami

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