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Boronic acid, [2,5-bis(dodecyloxy)-1,4-phenylene]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

211692-94-3

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211692-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 211692-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,6,9 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 211692-94:
(8*2)+(7*1)+(6*1)+(5*6)+(4*9)+(3*2)+(2*9)+(1*4)=123
123 % 10 = 3
So 211692-94-3 is a valid CAS Registry Number.

211692-94-3SDS

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 (4-borono-2,5-didodecoxyphenyl)boronic acid

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:211692-94-3 SDS

211692-94-3Downstream Products

211692-94-3Relevant academic research and scientific papers

Carbazole-containing conjugated copolymers as colorimetric/fluorimetric sensor for iodide anion

Vetrichelvan, Muthalagu,Nagarajan, Rajagopal,Valiyaveettil, Suresh

, p. 8303 - 8310 (2007/10/03)

A series of conjugated poly(p-phenylene carbazole) copolymers, poly(N-hexyl-3,6-carbazole-alt-2,5-bisdodecyloxyphenylene) [P1], poly(N-ethylhexyl-3,6-carbazole-alt-2,5-bisdodecyloxyphenylene) [P2], and poly(N-dodecyl-3,6-carbazole-alt-2,5-bisdodecyloxyphenylene) [P3] were prepared by using palladium-catalyzed Suzuki coupling reactions. All copolymers were characterized by means of FT-IR, GPC, 1H and 13C NMR, UV-vis, fluorescence spectroscopy, and X-ray powder diffraction patterns. All copolymers were soluble in common organic solvents, exhibited good thermal stability up to 390 °C, and showed UV-vis absorbance and fluorescence maxima around 328 and 394 nm, respectively. The polymers P1-P3 differed in N-alkyl substitution, i.e., n-hexyl (for P1), n-ethylhexyl (for P2), and n-dodecyl (for P3) groups. In addition, a third monomer, 2,5-substituted pyridine for poly(N-ethylhexyl-3,6-carbazole-co-2,5-didodecyloxy phenylene-co-2,5-pyridine) (P4) and dialkylated fluorene for poly(N-ethylhexyl-3,6-carbazole-co-2,5- didodecyloxy phenylene-co-9,9′-dihexylfluorene) (P5) was incorporated into the copolymer P2 to investigate the influence on their optical properties. The UV-vis and fluorescence maxima of P4 and P5 showed significant red shift in λmax by 29 and 19 nm and Δλem of 38 and 21 nm, respectively as compared to the polymers P1-P3. The quantum efficiencies of these polymers (52-78%) were relatively higher and may have good applications in the fabrication of LEDs. The UV-vis and fluorescence spectra of the polymers were significantly affected by the addition of tetrabutylammonium iodide and other metal iodides. A colorless polymer solution turns to deep yellow color on the addition of iodide salts. This change is, however, not observed in the presence of other anions such as fluoride, chloride and bromide salts. Therefore, the polymers P1-P5 may be useful in fabricating selective iodide sensors.

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