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Pyridine, 2-[4-(4-methylphenyl)-1,3-butadiynyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

117635-48-0

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117635-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 117635-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,6,3 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 117635-48:
(8*1)+(7*1)+(6*7)+(5*6)+(4*3)+(3*5)+(2*4)+(1*8)=130
130 % 10 = 0
So 117635-48-0 is a valid CAS Registry Number.

117635-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(4-methylphenyl)buta-1,3-diynyl]pyridine

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:117635-48-0 SDS

117635-48-0Relevant academic research and scientific papers

A convenient route to 1,3-diynes using ligand-free Cadiot–Chodkiewicz coupling reaction at room temperature under aerobic conditions

Asha, Sujatha,Anjana, Sasidharan,Thomas, Anns Maria,Thomas, Minu Elizabeth,Rohit,Krishnan, K. Keerthi,Ujwaldev, Sankuviruthiyil M,Anilkumar, Gopinathan

, p. 256 - 265 (2019/01/24)

In this study, we report a copper-catalyzed ligand-free Cadiot–Chodkiewicz coupling reaction. No additives or ligands are required for this Cu-catalyzed C(sp)–C(sp) coupling reaction of terminal alkynes with alkynyl halides. The low cost of copper catalyst, excellent yield of the products, suppression of side-products and mild reaction conditions are the major advantages of this protocol.

Highly efficient synthesis of unsymmetrical 1,3-diynes from organoalane reagents and alkynyl bromides mediated by a nickel catalyst

Mo, Song,Shao, Xue-Bei,Zhang, Gang,Li, Qing-Han

, p. 27243 - 27247 (2017/07/11)

Highly efficient and simple cross-coupling reactions of alkynylbromides with organoalane reagents for the synthesis of unsymmetrical 1,3-diynes derivatives using Ni(OAc)2 (2-5 mol%)/(o-furyl)3P (4-10 mol%) as a catalyst are reported. Excellent yields (up to 94%) were obtained for a wide range of substrates at rt or 60 °C for 2-3 h in Et2O or toluene.

Rapid access to unsymmetrical 1,3-diynes and 2,5-disubstituted thiophenes under ligand and Pd/Ni-free Cu-catalysis

Rao, Maddali L. N.,Islam, Sk Shamim,Dasgupta, Priyabrata

, p. 78090 - 78098 (2015/09/28)

A Pd/Ni-free copper-catalysed tandem synthesis was realized for rapid access to unsymmetrical 1,3-diynes from 1,1-dibromoalkenes and terminal alkynes. This method was extended to the straightforward synthesis of unsymmetrical 2,5-disubstituted thiophenes

Novel Synyhesis of Unsymmetrical Diarylbutadiynes

Nye, Susan Adams,Potts, Kevin T.

, p. 375 - 377 (2007/10/02)

Terminal arylbutadiynes, derived from 6-aryl-3,5-hexadin-2-ols, undergo a ready palladium-catalyzed coupling with activated aryl halides in the presence of a phase transfer catalyst to unsymmetrical diarylbutadiynes, not easily available by other coupling

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