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Benzene, 1,1'-(1,3-butadiyne-1,4-diyl)bis[4-fluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55606-94-5

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55606-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55606-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,0 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55606-94:
(7*5)+(6*5)+(5*6)+(4*0)+(3*6)+(2*9)+(1*4)=135
135 % 10 = 5
So 55606-94-5 is a valid CAS Registry Number.

55606-94-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-fluoro-4-[4-(4-fluorophenyl)buta-1,3-diynyl]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:55606-94-5 SDS

55606-94-5Relevant academic research and scientific papers

A copper based pillared-bilayer metal organic framework: Its synthesis, sorption properties and catalytic performance

Parshamoni, Srinivasulu,Sanda, Suresh,Jena, Himanshu Sekhar,Konar, Sanjit

, p. 7191 - 7199 (2014)

A new 2D pillared-bilayer flexible open metal organic framework {[Cu(tdc)(bpe)]n·2n(H2O)·n(MeOH)} (compound 1) [H2tdc = 2,5 thiophenedicarboxylic acid; bpe = 1,2-bis(4-pyridyl)ethane] has been synthesized through a solvent

Glycosyl Triazole Ligand for Temperature-Dependent Competitive Reactions of Cu-Catalyzed Sonogashira Coupling and Glaser Coupling

Mishra, Nidhi,Singh, Sumit K.,Singh, Anoop S.,Agrahari, Anand K.,Tiwari, Vinod K.

, p. 17884 - 17895 (2021/12/17)

Glycosyl triazoles have been introduced as efficient ligands for the Cu-catalyzed Sonogashira reaction to overcome the challenges of sideways homocoupling reactions in Cu catalysis in this reaction. The atmospheric oxygen in a sealed tube did not affect t

In Situ Synthesis of CuN4/Mesoporous N-Doped Carbon for Selective Oxidative Crosscoupling of Terminal Alkynes under Mild Conditions

Cao, Yue,Gu, Dong,Lei, Aiwen,Liang, Zhenjin,Su, Yaqiong,Wu, Jinsong,Wu, Yong,Xiao, Wei,Yang, Dali,Yu, Ruohan,Zhang, Dongchao,Zhang, Yuanteng

, (2021/12/23)

The 1,3-conjugated diynes are an important class of chemical intermediates, and the selective crosscoupling of terminal alkynes is an efficient chemical process for manufacturing asymmetrical 1,3-conjugated diynes. However, it often occurs in homogenous conditions and costs a lot for reaction treatment. Herein, a copper catalyzed strategy is used to synthesize highly ordered mesoporous nitrogen-doped carbon material (OMNC), and the copper species is in situ transformed into the copper single-atom site with four nitrogen coordination (CuN4). These features make the CuN4/OMNC catalyst efficient for selective oxidative crosscoupling of terminal alkynes, and a wide range of asymmetrical and symmetrical 1,3-diynes (26 examples) under mild conditions (40?°C) and low substrates ratio (1.3). Density functional theory (DFT) calculations reveal that the aryl–alkyl crosscoupling has the lowest energy barrier on the CuN4 site, which can explain the high selectivity. In addition, the catalyst can be separated and reused by simply centrifugation or filtration. This work can open a facile avenue for constructing single-atom loaded mesoporous materials to bridge homogeneous and heterogeneous catalysis.

Preparation method of water-soluble vitamin E participated conjugated diyne compound

-

Paragraph 0077-0081, (2021/11/14)

The water-soluble vitamin E participates in the green preparation method of the conjugated diyne compound, the water serves as a reaction solvent, the use amount of the organic solvent is reduced, and zero emission of the solvent is realized. The excellent physicochemical properties of water are fully utilized, the reaction conditions are mild and efficient, the surfactant TPGS - 750 - M can be recycled through treatment, and the principle of environmental friendliness is completely met. The reaction substrate is wide in applicability, can catalyze the aryl alkyne, can catalyze the aliphatic hydrocarbon, and provides a simple and environment-friendly preparation method for the synthesis of the conjugated diyne. The copper catalyst which is more suitable for the reaction and reaction medium of the invention is screened out, and the yield is greatly improved.

Leaf-like CuO nanosheets on rGO as an efficient heterogeneous catalyst for Csp-Csp homocoupling of terminal alkynes

Gao, Lingfeng,Wang, Bin,Zheng, Gengxiu

, (2020/12/21)

In this work, the economic and well-defined leaf-like CuO nanosheets on rGO (CuO nanosheets/rGO) was synthesized by a convenient hydrothermal method. The morphology and chemical composition of CuO nanosheets/rGO were confirmed by XRD, SEM-EDS, TEM, HR-TEM, and XPS techniques. The CuO nanosheets/rGO was successfully applied as a high-performance heterogeneous catalyst in the homocoupling of 12 terminal alkynes, and the isolated yield of each product was more than 80%, except for propargyl alcohol. This catalyst could be reused five times with little activity loss. Thus, it is beneficial for green and sustainable development of organic synthetic chemistry.

Cu-Catalyzed solvent-free, pot-economic synthesis of 1,3-dynes from 1,1-dibromoalkenes in the presence of DBU?H2O

Moodapelly, Shiva Krishna,Nanaji, Yerramsetti,Sharma, Gangavaram V.M.,Suneeel, Kanaparthy,Doddi, Venkata Ramana

, (2021/05/27)

An efficient synthesis of 1,3-diynes directly from 1,1-dibromoalkenes has been achieved by utilizing hydrated 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU.H2O) as a sole reagent and a catalyst CuI. In general, 1,3-diynes were synthesized from corresponding terminal alkynes, which in turn were obtained from 1,1-dibromoalkenes. The DBU.H2O allowed the synthesis of 1,3-diynes not only in a pot-efficient manner but also under solvent-free conditions at ambient temperature. A plausible mechanism is proposed via 1-bromoalkynes intermediate instead of terminal alkynes.

Synthesis of 1,3-Diynes Using Calcium Carbide as an Alkyne Source

Liu, Zhenrong,Li, Zheng

, p. 302 - 308 (2020/12/11)

A simple method for the synthesis of 1,3-diynes from iodoarenes using calcium carbide as an alkyne source and air as an oxidant is described. A series of 1,4-diarylbuta-1,3-diynes were efficiently synthesized by this strategy. The salient features of this protocol are the use of inexpensive and easy-to-handle alkyne source, broad substrate scope, open-air condition, and simple operation procedure.

Reduced graphene oxide supported copper oxide nanocomposites: An efficient heterogeneous and reusable catalyst for the synthesis of ynones, 1,3-diynes and 1,5-benzodiazepines in one-pot under sustainable reaction conditions

Sarkar, Rajib,Gupta, Ajay,Jamatia, Ramen,Pal, Amarta Kumar

, (2020/03/16)

A greener and efficient method for the synthesis of ynones and 1,3-diynes using copper oxide nanoparticles (CuONPs) doped reduced graphene oxide (CuO@rGO) catalyst under palladium, ligand and solvent free conditions have been developed. The catalyst was s

Functionalization of graphene oxide sheets with magnetite nanoparticles for the adsorption of copper ions and investigation of its potential catalytic activity toward the homocoupling of alkynes under green conditions

Baouab, Mohammed Hassen V.,Beyou, Emmanuel,Chaabane, Laroussi,Luneau, Dominique

, p. 91 - 103 (2020/05/29)

This paper deals with the preparation of graphene oxide sheets (GO) modified with magnetite nanoparticles (Fe3O4NPs) for removing Cu(II) ions from aqueous solutions. Moreover, the recovered Cu(II)-based material was recycled as a cat

Trithiocarbonate Anion as a Sulfur Source for the Synthesis of 2,5-Disubstituted Thiophenes and 2-Substituted Benzo[ b]thiophenes

Paix?o, Douglas B.,Rampon, Daniel S.,Salles, Helena D.,Soares, Eduardo G. O.,Bilheri, Filipe N.,Schneider, Paulo H.

supporting information, p. 12922 - 12934 (2020/11/26)

The trithiocarbonate anion (CS32-) was generated in situ from CS2 and KOH in dimethyl sulfoxide by a simple method and used as a novel synthetic equivalent of the S2- synthon for the synthesis of 2,5-disubstituted thiophenes from 1,3-butadiynes. Additionally, this system was employed for the metal-free synthesis of 2-substituted benzo[b]thiophenes from 2-haloalkynyl (hetero)arenes. These compounds were obtained from a cheap and readily available sulfur source in moderate to good yields, with good functional group tolerance.

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