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Benzene, 1-bromo-4-[(4-octylphenyl)ethynyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62856-18-2

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62856-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62856-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,5 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62856-18:
(7*6)+(6*2)+(5*8)+(4*5)+(3*6)+(2*1)+(1*8)=142
142 % 10 = 2
So 62856-18-2 is a valid CAS Registry Number.

62856-18-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4-[2-(4-octylphenyl)ethynyl]benzene

1.2 Other means of identification

Product number -
Other names 1-(4-n-octylphenyl)-2-(4-bromophenyl)acetylene

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:62856-18-2 SDS

62856-18-2Relevant academic research and scientific papers

Synthesis and photoluminescence properties of heterocycle-containing poly(disubstituted acetylene)s

Muroga, Tatsuoki,Sakaguchi, Toshikazu,Hashimoto, Tamotsu

, p. 4380 - 4387 (2012/11/13)

The metathesis polymerizations of disubstituted acetylenes containing heterocycles such as thiophene, furan, benzo[b]thiophene, and benzothiazole were examined using NbCl5, TaCl5, and WCl6. Thiophene-containing monomers polymerized to afford relatively high-molecular-weight polymers in moderate yields. Benzo[b]thiophene-containing monomers also polymerized to give polymers with relatively high molecular weights. On the other hand, furan- and benzothiazole-containing monomers exhibited low metathesis polymerizability, and the polymerizations did not provide high-molecular-weight polymers. Poly(1-hexyl-2-arylacetylene)s having heterocycles [poly(1a) and poly(3a), Scheme 1] emitted blue-colored lights, and the emission maxima were around 480 nm. Heterocycle-containing poly(1-phenyl-2-arylacetylene) [poly(1b)] and poly(1-fluorenyl-2-arylacetylene) [poly(3d)] showed green-colored and yellow-colored emissions, and the emission maxima were 520 and 540 nm, respectively. The emission wavelengths of poly(disubstituted acetylene)s having heterocycles were almost the same as those of the corresponding poly(disubstituted acetylene)s without heterocycles. However, heterocycle-containing polymers showed high fluorescence quantum yields compared to the corresponding polymers without heterocycles. Diarylacetylene polymers showed emission red-shifts between the solution and cast film, while the emission maximum of poly(1-hexyl-2-phenylacetylene) [poly(1a)] in the cast film was almost the same as that in the solution. Benzo[b]thiophene-containing poly(1-(4-trimethylsilylphenyl)-2-phenylacetylene) [poly(3b)] and poly(1-(9,9-dimethyl-2-fluorenyl)-2-phenylacetylene) [poly(3d)] afforded the free-standing membranes because of their high molecular weights. The oxygen permeability coefficient (PO2) of poly(3b) was as large as 1400 barrers. Poly(3d) showed higher gas permeability, and its PO2 was 5300 barrers.

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