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18442-29-0

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18442-29-0 Usage

Physical form

Crystalline, yellow solid

Solubility

Insoluble in water, soluble in organic solvents

Use in organic synthesis

Building block for the production of advanced materials

Applications

Liquid crystals, organic light-emitting diodes, high-performance electronic and optoelectronic devices

Unique properties

Electronic and optical properties

Potential future applications

Molecular electronics, nanotechnology

Check Digit Verification of cas no

The CAS Registry Mumber 18442-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,4 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18442-29:
(7*1)+(6*8)+(5*4)+(4*4)+(3*2)+(2*2)+(1*9)=110
110 % 10 = 0
So 18442-29-0 is a valid CAS Registry Number.

18442-29-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethynyl-2-(2-ethynylphenyl)benzene

1.2 Other means of identification

Product number -
Other names 2,2'-DIETHYNYL-1,1'-BIPHENYL

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:18442-29-0 SDS

18442-29-0Relevant articles and documents

Copper-Catalyzed Chemoselective Silylative Cyclization of 2,2′-Diethynylbiaryl Derivatives

Zhao, Meng,Wang, Ying,Wang, Zi-Lu,Xu, Jian-Lin,Dai, Kai-Yang,Xu, Yun-He

supporting information, p. 3859 - 3863 (2021/05/26)

In this protocol, copper-catalyzed diverse silylative carbocyclization reactions of 2,2′-diethynylbiaryl derivatives with silaboronate were reported. Three new and novel types of domino reactions for the copper-catalyzed transformation of silaboronate were discovered. The corresponding cyclobuta[l]phenanthrene, bis((silyl)methyl)phenanthrene, and silyl-substituted exocyclic diene products were chemoselectively formed with high efficiency.

Ruthenium-Catalyzed Cycloisomerization of 2,2′-Diethynyl- biphenyls Involving Cleavage of a Carbon-Carbon Triple Bond

Matsuda, Takanori,Kato, Kotaro,Goya, Tsuyoshi,Shimada, Shingo,Murakami, Masahiro

supporting information, p. 1941 - 1943 (2016/02/14)

A ruthenium complex catalyzes a new cycloisomerization reaction of 2,2′-diethynylbiphenyls to form 9-ethynylphenanthrenes, thereby cleaving the carbon-carbon triple bond of the original ethynyl group. A metal-vinylidene complex is generated from one of th

Synthesis of a 2D lander

Basu, Chaitali,Barthes, Cecile,Sadhukhan, Subir K.,Girdhar, Navdeep K.,Gourdon, Andre

, p. 136 - 140 (2007/10/03)

A method for the preparation of an asymmetric superbenzene is presented. The synthesis proceeds through the 12-fold cyclodehydrogenation of a polyaromatic precursor obtained by successive Diels-Alder additions of cyclopentadienones and alkynes. Wiley-VCH

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