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133997-05-4

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133997-05-4 Usage

General Description

4-(N-Octyl)benzeneboronic acid is an organic compound with the chemical formula C14H23BO2. It is a boronic acid derivative with an octyl group attached to the benzene ring. 4-(N-OCTYL)BENZENEBORONIC ACID is commonly used as a building block in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals and agrochemicals. It is also utilized as a ligand in various catalytic reactions, such as Suzuki-Miyaura cross-coupling and Negishi coupling, due to its ability to complex with transition metals. 4-(N-Octyl)benzeneboronic acid has demonstrated promising potential as a versatile and useful reagent in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 133997-05-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,9,9 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 133997-05:
(8*1)+(7*3)+(6*3)+(5*9)+(4*9)+(3*7)+(2*0)+(1*5)=154
154 % 10 = 4
So 133997-05-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H23BO2/c1-2-3-4-5-6-7-8-13-9-11-14(12-10-13)15(16)17/h9-12,16-17H,2-8H2,1H3

133997-05-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-octylphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 4-octylbenzeneboronic 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:133997-05-4 SDS

133997-05-4Relevant articles and documents

Design, synthesis and biological activity of sphingosine kinase 2 selective inhibitors

Raje, Mithun R.,Knott, Kenneth,Kharel, Yugesh,Bissel, Philippe,Lynch, Kevin R.,Santos, Webster L.

scheme or table, p. 183 - 194 (2012/02/06)

Sphingosine kinase (SphK) has emerged as an attractive target for cancer therapeutics due to its role in cell survival. SphK phosphorylates sphingosine to form sphingosine 1-phosphate (S1P), which has been implicated in cancer growth and survival. SphK ex

A deeper insight into the dithiocarbamate precursor route: Synthesis of soluble poly(thienylene vinylene) derivatives for photovoltaic applications

Dilien, Hanne,Palmaerts, Arne,Lenes, Martijn,De Boer, Bert,Blom, Paul,Cleij, Thomas J.,Lutsen, Laurence,Vanderzande, Dirk

scheme or table, p. 10231 - 10240 (2011/08/03)

The synthesis of, two new poly(thienylene vinylene) derivatives is described, i.e. poly(3-octyl-2,5-thienylene vinylene) (O-PTV) and poly(bis[octylphenyl-2,5-thienylene vinylene]) (BOP-PTV). Both polymers have been prepared via the dithiocarbamate (DTC) precursor route. The polymerization protocol of the monomer toward the precursor polymer has been optimized by the use of different bases, leading to improved reproducibility of the polymerization step. Processability has been guaranteed by the introduction of alkyl side chains. Finally the precursor polymers were converted toward conjugated polymers and they were fully characterized by UV/vis, IR, GPC, and cyclic voltammetry. Bulk heterojunction solar cells with PCBM as acceptor showed promising power conversion efficiencies of 0.80% for BOP-PTV and 0.92% for O-PTV.

DIIMIDE-BASED SEMICONDUCTOR MATERIALS AND METHODS OF PREPARING AND USING THE SAME

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Page/Page column 41, (2008/12/05)

Diimide-based semiconductor materials are provided with processes for preparing the same. Composites and electronic devices including the diimide-based semiconductor materials also are provided.

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