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Naphthalene, 6-(5-hexynyl)-1,2,3,4-tetrahydro- is a chemical compound with the molecular formula C16H18. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, with a 5-hexynyl group attached to the 6th carbon position. Naphthalene, 6-(5-hexynyl)-1,2,3,4-tetrahydro- is characterized by its unique structure, which features a hexynyl chain extending from the naphthalene core. It is an organic molecule with potential applications in various chemical and pharmaceutical industries, such as the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its specific structure, it may exhibit unique chemical properties and reactivity compared to other naphthalene derivatives.

1914-36-9

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1914-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1914-36-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1914-36:
(6*1)+(5*9)+(4*1)+(3*4)+(2*3)+(1*6)=79
79 % 10 = 9
So 1914-36-9 is a valid CAS Registry Number.

1914-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[Hexin-(5)-yl]3.4-tetramethylen-benzol

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

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More Details:1914-36-9 SDS

1914-36-9Downstream Products

1914-36-9Relevant academic research and scientific papers

Activation of Carbon Dioxide: Nickel-Catalyzed Electrochemical Carboxylation if Diynes

Derien, Sylvie,Clinet, Jean-Claude,Dunach, Elisabet,Perichon, Jacques

, p. 2578 - 2588 (2007/10/02)

The simualtaneous activation of carbon dioxide and diynes by electrogenerated LNi(0) complexes (L=bpy, pentamethyldiethylenetriamine: PMDTA) enables the selective incorporation of one molecule of CO2 into the unsaturated systems and the preparative-scale

From Stoichiometry to Catalysis: Electroreductive Coupling of Alkynes and Carbon Dioxide with Nickel-Bipyridine Complexes. Magnesium Ions as the Key for Catalysis

Derien, Sylvie,Dunach, Elisabet,Perichon, Jacques

, p. 8447 - 8454 (2007/10/02)

The incorporation of carbon dioxide into nonactivated alkynes catalyzed by electrogenerated nickel-bipyridine complexes affords α,β-unsaturated acids in moderate to good yields.The electrocarboxylation reaction was undertaken on a preparative scale in the presence of a sacrificial magnesium anode: the formation of acids from alkynes is stoichiometric with respect to the nickel complex if performed in a two-compartment cell but can be made catalytic in a single-compartment cell.An intermediate nickelacycle was isolated from the reaction with 4-octyne.The cleavage ofthis metallacycle by magnesium ions is the key step to explain catalysis.

Electrogenerated nickel(0) catalyzed carbon dioxide incorporation into α,ω-diynes

Derien, S.,Dunach, E.,Perichon, J.

, p. C43 - C46 (2007/10/02)

Electrogenerated low-valent nickel complexes are active catalysts for carbon dioxide incorporation into α,ω-diynes.A strong influence of the nature of the ligand on the selectivity of this carboxylation has been observed.

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