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121219-08-7

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121219-08-7 Usage

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suzuki reaction

Check Digit Verification of cas no

The CAS Registry Mumber 121219-08-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,2,1 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 121219-08:
(8*1)+(7*2)+(6*1)+(5*2)+(4*1)+(3*9)+(2*0)+(1*8)=77
77 % 10 = 7
So 121219-08-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H19BO3/c1-2-3-4-5-10-16-12-8-6-11(7-9-12)13(14)15/h6-9,14-15H,2-5,10H2,1H3

121219-08-7 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (H1357)  4-Hexyloxyphenylboronic Acid (contains varying amounts of Anhydride)  

  • 121219-08-7

  • 1g

  • 390.00CNY

  • Detail
  • TCI America

  • (H1357)  4-Hexyloxyphenylboronic Acid (contains varying amounts of Anhydride)  

  • 121219-08-7

  • 5g

  • 1,250.00CNY

  • Detail
  • Alfa Aesar

  • (H52874)  4-n-Hexyloxybenzeneboronic acid, 96%   

  • 121219-08-7

  • 1g

  • 972.0CNY

  • Detail
  • Alfa Aesar

  • (H52874)  4-n-Hexyloxybenzeneboronic acid, 96%   

  • 121219-08-7

  • 5g

  • 3889.0CNY

  • Detail

121219-08-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Hexyloxyphenylboronic acid

1.2 Other means of identification

Product number -
Other names (4-hexoxyphenyl)boronic acid

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:121219-08-7 SDS

121219-08-7Relevant articles and documents

A novel trigeminal zinc porphyrin and corresponding porphyrin monomers for dye-sensitized solar cells

Chen, Bin,Li, Xin,Wu, Wenjun,Zha, Quanzheng,Xie, Yongshu

, p. 10439 - 10449 (2014)

A novel trigeminal zinc porphyrin sensitizer (T) and two zinc porphyrin monomers (M1 and M2) were successfully designed and synthesized. The spectral, electrochemical, and photovoltaic properties of the porphyrin dyes were investigated. Compared with M1, the molecule of M2 has an additional aliphatic n-hexyloxyl chain at the meso-position of the porphyrin framework, and such a structure is favorable for the formation of a compact hydrophobic layer at the TiO2 surface and the retardation of the diffusion of I 3- ions into the nanoporous TiO2 electrode, resulting in more effective suppression of the charge recombination process and a higher Voc. Meanwhile, M2 has larger IPCE values than those of M1, leading to the higher Jsc value. Thus, the DSSC devices based on M2 demonstrated a relatively high power conversion efficiency of 5.77%, with the Jsc, Voc and ff values of 13.93 mA cm-2, 732 mV, and 0.566, respectively. Even though dye T has the highest molar absorption coefficients and multiple binding moieties, the corresponding power conversion efficiency is 2.30%, which is lower than those for M1 and M2. These observations may be ascribed to the low efficiency of the electron injection process caused by the isolation of the LUMOs from the anchoring carboxyl groups in addition to the lowest adsorption amount.

CYCLOHEXADIENE FULLERENE DERIVATIVES

-

, (2015/03/28)

The invention relates to novel fullerene derivatives, to methods for their preparation and educts or intermediates used therein, to mixtures and formulations containing them, to the use of the fullerene derivatives, mixtures and formulations as organic semiconductors in, or for the preparation of, organic electronic (OE) devices, especially organic photovoltaic (OPV) devices and organic photodetectors (OPD), and to OE, OPV and OPD devices comprising, or being prepared from, these fullerene derivatives, mixtures or formulations.

Photoswitchable triple hydrogen-bonding motif

Herder, Martin,Paetzel, Michael,Grubert, Lutz,Hecht, Stefan

supporting information; experimental part, p. 460 - 462 (2011/02/28)

Photochromic bis(thiazol-4-yl)maleimides, displaying enhanced binding affinity to complementary melamine receptors in their ring-closed switching state, have been developed and could pave the way to light-responsive supramolecular assemblies.

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